AU741806B2 - Thermal cycler for automatic performance of the polymerase chain reaction with close temperature control - Google Patents

Thermal cycler for automatic performance of the polymerase chain reaction with close temperature control Download PDF

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Publication number
AU741806B2
AU741806B2 AU97002/98A AU9700298A AU741806B2 AU 741806 B2 AU741806 B2 AU 741806B2 AU 97002/98 A AU97002/98 A AU 97002/98A AU 9700298 A AU9700298 A AU 9700298A AU 741806 B2 AU741806 B2 AU 741806B2
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Australia
Prior art keywords
sample
temperature
block
power
tubes
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AU97002/98A
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AU9700298A (en
Inventor
John Girdner Atwood
Lisa May Goven
Richard Leath
Marcel Margulies
Albert Carmelo Mossa
Robert P Ragusa
Fenton Williams
Timothy M. Woudenberg
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Applied Biosystems LLC
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Perkin Elmer Corp
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Priority claimed from AU24934/95A external-priority patent/AU696482B2/en
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Publication of AU9700298A publication Critical patent/AU9700298A/en
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Publication of AU741806B2 publication Critical patent/AU741806B2/en
Assigned to APPLERA CORPORATION reassignment APPLERA CORPORATION Assignment by Patentee under S 187, Reg 19.1 Assignors: PERKIN-ELMER CETUS INSTRUMENTS
Assigned to APPLIED BIOSYSTEMS, LLC reassignment APPLIED BIOSYSTEMS, LLC Assignment by Patentee under S 187, Reg 19.1 Assignors: APPLERA CORPORATION
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Classifications

    • GPHYSICS
    • G05CONTROLLING; REGULATING
    • G05DSYSTEMS FOR CONTROLLING OR REGULATING NON-ELECTRIC VARIABLES
    • G05D23/00Control of temperature
    • G05D23/19Control of temperature characterised by the use of electric means
    • G05D23/1927Control of temperature characterised by the use of electric means using a plurality of sensors
    • G05D23/193Control of temperature characterised by the use of electric means using a plurality of sensors sensing the temperaure in different places in thermal relationship with one or more spaces
    • G05D23/1935Control of temperature characterised by the use of electric means using a plurality of sensors sensing the temperaure in different places in thermal relationship with one or more spaces using sequential control
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/508Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above
    • B01L3/5085Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above for multiple samples, e.g. microtitration plates
    • B01L3/50851Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above for multiple samples, e.g. microtitration plates specially adapted for heating or cooling samples
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/508Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above
    • B01L3/5085Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above for multiple samples, e.g. microtitration plates
    • B01L3/50853Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above for multiple samples, e.g. microtitration plates with covers or lids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L7/00Heating or cooling apparatus; Heat insulating devices
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L7/00Heating or cooling apparatus; Heat insulating devices
    • B01L7/52Heating or cooling apparatus; Heat insulating devices with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples
    • GPHYSICS
    • G05CONTROLLING; REGULATING
    • G05DSYSTEMS FOR CONTROLLING OR REGULATING NON-ELECTRIC VARIABLES
    • G05D23/00Control of temperature
    • G05D23/19Control of temperature characterised by the use of electric means
    • G05D23/1917Control of temperature characterised by the use of electric means using digital means
    • GPHYSICS
    • G05CONTROLLING; REGULATING
    • G05DSYSTEMS FOR CONTROLLING OR REGULATING NON-ELECTRIC VARIABLES
    • G05D23/00Control of temperature
    • G05D23/19Control of temperature characterised by the use of electric means
    • G05D23/1919Control of temperature characterised by the use of electric means characterised by the type of controller
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/14Process control and prevention of errors
    • B01L2200/143Quality control, feedback systems
    • B01L2200/147Employing temperature sensors
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/04Closures and closing means
    • B01L2300/041Connecting closures to device or container
    • B01L2300/042Caps; Plugs
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/04Closures and closing means
    • B01L2300/046Function or devices integrated in the closure
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/08Geometry, shape and general structure
    • B01L2300/0809Geometry, shape and general structure rectangular shaped
    • B01L2300/0829Multi-well plates; Microtitration plates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/18Means for temperature control
    • B01L2300/1805Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks
    • B01L2300/1822Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks using Peltier elements
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/18Means for temperature control
    • B01L2300/1805Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks
    • B01L2300/1827Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks using resistive heater
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/18Means for temperature control
    • B01L2300/1838Means for temperature control using fluid heat transfer medium
    • B01L2300/185Means for temperature control using fluid heat transfer medium using a liquid as fluid
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/508Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above
    • B01L3/5082Test tubes per se

Description

S F Ref: 307640D1
AUSTRALIA
PATENTS ACT 1990 COMPLETE SPEIFICATION FOR A STANDARD PATENT 0 0000 0@ *0 0
ORIGINAL
Name and Address of Applicant: 0e* 0 S 00 0 0 0 ooze 0 0000
S
0 S 0 Actual Inventor(s): Perkin-Elmer Cetus Instruments 1400 Fifty-Third Street Emeryville California 94608 UNITED STATES OF AMERICA Albert Carmelo Mossa, Lisa May Goven, John Girdner Atwood, Fenton Williams, Timothy M Woudenberg, Marcel Margulles, Robert P Ragusa, Richard Leath Spruson Ferguson, Patent Attorneys Level 33 St Martins Tower, 31 Market Street Sydney, New South Wales, 2000, Australia Thermal Cycler for Automatic Performance of the Polymerase Chain Reaction with Close Temperature Control Address for Service: Invention Title: The following statement is a full description of this invention, best method of performing it known to me/us:including the 5845 1 THERMAL CYCLER FOR AUTOMATIC PERFORMn CE THE RrSECHAIN CTION WIT CLOS
O
Background Of the Invention 0.0 00.
0 0000 00 0 00 0000 00 @0 0 0 00 *00 0 00 0S 0 0 0
S
The invention pertains to the field of computer directed instruments for performing the polymerase chain 10 reaction (hereafter PCR). More particularly, the invention pertains to automated instruments that can perform the polymerase chain reaction simultaneously on many samples with a very high degree of precision as to results obtained for each sample. This high precision provides the capability, among other things, of performing so-called "quantitative
PCR".
To amplify DNA (Deoxyribose Nucleic Acid) using the PCR process, it is necessary to cycle a specially constituted liquid reaction mixture through a PCR protocol includin 20 several different temperature incubation periods. The reaction mixture is comprised of various components such as the DNA to be amplified and at least two primers selected in a predetermined way so as to be sufficiently compl-qentary to the sample DNA as to be able to create extension products of the DNA to be amplified. The reaction mixture includes various enzymes and/or other reagents, as well as several deoxyribonucleoside triphosphates such as dATP, dCTP, dGTP and dTTP. Generally, the primers are oligonucleotides which are capable of acting as a point of initiation of synthesis when placed under conditions in which synthesis of a primer extension product which is complimentary to a nucleic acid strand is induced, in the presence of nucleotides and inducing agents such as thermostable DNA polymerase at a suitable temperature and pH.
The Polymerase Chain Reaction (PCR) has proven a 2phenomenally successful technology for genetic analysis largely because it is so simple and requires relatively low cost instrumentation. A key to PCR is the concept of thermocycling: alternating steps of melting DNA, annealing short primers to the resulting single strands, and extending those primers to make new copies of double stranded DNA. In thermocycling, the PCR reaction mixture is repeatedly cycled from high temperatures (>90o C) for melting the DNA, to lower temperatures (40oC to 70 0 C) for primer annealing and extension. The first commercial system for performing the S* thermal cycling required in the polymerase chain reaction, the Perkin-Elmer Cetus DNA Thermal Cycler, was introduced in 1987.
Applications of PCR technology are now moving from basic S. 15 research to applications in which large numbers of similar amplifications are routinely run. These areas include diagnostic research, biopharmaceutical development, genetic analysis, and environmental testing. Users in these areas would benefit from a high performance PCR system that would S 20 provide the user with high throughput, rapid turn-around time, and reproducible results. Users in these areas must be assured of reproducibility from sample-to-sample, run-torun, lab-to-lab, and instrument-to-instrument.
For example, the physical mapping process in the Human 25 Genome Project may become greatly simplified by utilizing sequence tagged sites. An STS is a short, unique sequice easily amplified by PCR and which identifies a location on the chromosome. Checking for such sites to make genome maps requires amplifying large numbers of samples in a short time with protocols which can be reproducibly run throughout the world.
As the number of PCR samples increases, it becomes more important to integrate amplification with sample preparation and post-amplification analysis. The sample vessels must not only allow rapid thermal cycling but also permit more automated handling for operations such as solvent 3 O extractions and centrifugation. The vessels should work consistently at low volumes, to reduce reagent costs.
Generally PCR temperature cycling involves at least two incubations at different temperatures. One of these incubations is for primer hybridization and a catalyzed primer extension reaction. The other incubation is for denaturation, separation of the double stranded extension products into single strand templates for use in the next hybridization and extension incubation interval.
10 The details of the polymerase chain reaction, the temperature cycling and reaction conditions necessary for PCR as well as the various reagents and enzymes necessary to perform the reaction are described in U.S. patents 4,683,202, 4,683,195, EPO Publication 258,017 and 4,889,818 15 (Taq polymerase enzyme patent) and all other PCR patents which are assigned to Cetus Corporation, which are hereby incorporated by reference.
The purpose of a polymerase chain reaction is to manufacture a large volume of DNA which is identical to an initially supplied small volume of "seed" DNA. The reaction involves copying the strands of the DNA and then using the copies to generate other copies in subsequent cycles. Under ideal conditions, each cycle will double the amount of DNA present thereby resulting in a geometric progression in the volume of copies of the "target" or "seed" DNA strnds S* present in the reaction mixture.
A typical PCR temperature cycle requires that the reaction mixture be held accurately at each incubation temperature for a prescribed time and that the identical cycle or a similar cycle be repeated many times. A typical PCR program starts at a sample temperature of 94C held for seconds to denature the reaction mixture. Then, the temperature of the reaction mixture is lowered to 370C and held for one minute to permit primer hybridization. Next, the temperature of the reaction mixture is raised to a temperture in the range from 500C to 720C where it is held 4 Sfor two minutes to promote the synthesis of extension products. This completes one cycle. The next PCR cycle then starts by raising the temperature of the reaction mixture to 94 0 C again for strand separation of the extension products., formed in the previous cycle (denaturation).
Typically, the cycle is repeated 25 to 30 times.
Generally, it is desirable to change the sample temperature to the next temperature in the cycle as rapidly as possible for several reasons. First, the chemical 10 reaction has an optimum temperature for each of its stages.
see. Thus, less time spent at nonoptimum temperatures means a better chemical result is achieved. Another reason is--that a minimum time for holding the reaction mixture at each incubation temperature is required after each said 15 incubation temperature is reached. These minimum incubation times establish the "floor" or minimum time it takes to complete a cycle. Any time transitioning between sample incubation temperatures is time which is added to this minimum cycle time. Since the number of cycles is fairly 20 large, this additional time unnecessarily lengthens the C total time needed to complete the amplification.
In some prior automated PCR instruments, the reaction mixture was stored in a disposable plastic tube which is closed with a cap. A typical sample volume for such tubes was approximately 100 microliters. Typically, such instruments used many such tubes filled with sample DNAand reaction mixture inserted into holes called sample wells in a metal block. To perform the PCR process, the temperature of the metal block was controlled according to prescribed temperatures and times specified by the user in a PCR protocol file. A computer and associated electronics then controlled the temperature of the metal block in accordance with the user supplied data in the PCR protocol file defining the times, temperatures and number of cycles, etc.
As the metal block changed temperature, the samples in the various tubes followed with similar changes in temperature.
5 However, in these prior art instruments not all samples experienced exactly the same temperature cycle. In these prior art PCR instruments, errors in sample temperature were generated by nonuniformity of temperature from place to place within the metal sample block, temperature gradients existed within the metal of the block thereby causing some samples to have different temperatures than other samples at particular times in the cycle. Further, there were delays in transferring heat from the sample block 10 to the sample, but the delays were not the same for all samples. To perform the PCR process successfully and efficiently, and to enable so called "quantitative"-PCR, these time delays and temperature errors must be minimized to a great extent.
0 e 15 The problems of minimizing time delays for heat S transfer to and from the sample liquid and minimizing temperature errors due to temperature gradients or nonuniformity in temperature at various points on the metal block become particularly acute when the size of the region 20 containing samples becomes large. It is a highly desirable attribute for a PCR instrument to have a metal block which is large enough to accommodate 96 sample tubes arranged in the format of an industry standard microtiter plate.
The microtiter plate is a widely used means for handling, processing and analyzing large numbers of small samples in the biochemistry and biotechnology fields.
Typically, a microtiter plate is a tray which is 3 5/8 inches wide and 5 inches long and contains 96 identical sample wells in an 8 well by 12 well rectangular array on 9 millimeter centers. Although microtiter plates are available in a wide variety of materials, shapes and volumes of the sample wells, which are optimized for many different uses, all microtiter plates have the same overall outside dimensions and the same 8 x 12 array of wells on 9 millimeter centers. A wide variety of equipment is available for automating the handling, processing and 6 analyzing of samples in this standard microtiter plate format.
Generally microtiter plates are made of injection molded or vacuum formed plastic and are inexpensive and considered disposable. Disposability is a highly desirable characteristic because of the legal liability arising out of cross contamination and the difficulty of washing and drying microtiter plates after use.
It is therefore a highly desirable characteristic for 10 a PCR instrument to be able to perform the PCR reaction on up to 96 samples simultaneously said samples being arranged in a microtiter plate format.
Of course, the size of the metal block which is necessary to heat and cool 96 samples in an 8 x 12 well 15 array on 9 millimeter centers is fairly large. This large area block creates multiple challenging engineering problems for the design of a PCR instrument which is capable of heating and cooling such a block very rapidly in a temperature range generally from 0 to 1000C with very little 20 tolerance for temperature variations between samples. These problems arise from several sources. First, the large thermal mass of the block makes it difficult to move the block temperature up and down in the operating range with great rapidity. Second, the need to attach the block to various external devices such as manifolds for supply and withdrawal of cooling liquid, block support attachment 0 points, and associated other peripheral equipment creates the potential for temperature gradients to exist across the block which exceed tolerable limits.
There are also numerous other conflicts between the requirements in the design of a thermal cycling system for automated performance of the PCR reaction or other reactions requiring rapid, accurate temperature cycling of a large number of samples. For example, to change the temperature of a metal block rapidly, a large amount of heat must be added to, or removed from the sample block in a short period 7 of time. Heat can be added from electrical resistance heaters or by flowing a heated fluid in contact with the block. Heat can be removed rapidly by flowing a chilled fluid in contact with the block. However, it is seemingly impossible to add or remove large amounts of heat rapidly in a metal block by these means without causing large differences in temperature from place to place in the block thereby forming temperature gradients which can result in nonuniformity of temperature among the samples.
o .10 Even after the process of addition or removal of heat is terminated, temperature gradients can persist for a time roughly proportional to the square of the distance that- the heat stored in various points in the block must travel to cooler regions to eliminate the temperature gradient. Thus, 15 as a metal block is made larger to accommodate more samples, the time it takes for temperature gradients existing in the block to decay after a temperate change causes temperature gradients which extend across the largest dimensions of the block can become markedly longer. This makes it 20 increasingly difficult to cycle the temperature of the S:'o sample block rapidly while maintaining accurate temperature uniformity among all the samples.
Because of the time required for temperature gradients to dissipate, an important need has arisen in the design of a high performance PCR instrument to prevent the creation of s .e temperature gradients that extend over large distances in the block. Another need is to avoid, as much as possible, the requirement for heat to travel across mechanical boundaries between metal parts or other peripheral equipment attached to the block. It is difficult to join metal parts in a way that insures uniformly high thermal conductance everywhere across the joint. Nonuniformities of thermal conductance will generate unwanted temperature gradients.
Summary of the Invention According to the teachings of the invention, there is 8 disclosed herein a thin walled sample tube for decreasing the delay between changes in sample temperature of the sample block and corresponding changes in temperature of the reaction mixture. Two different sample tube sizes are disclosed, but each has a thin walled conical section that fits into a matching conical recess in the sample block.
Typically, cones with 170 angles relative to the longitudinal axis are used to prevent jamming of the tubes into the sample block but to allow snug fit. Other shapes 10 and angles would also suffice for purposes of practicing the invention.
•Also, other types of heat exchangers can also be-used Sother than sample blocks such as liquid baths, ovens, etc.
However, the wall thickness of the section of the sample 15 tube which is in contact with whatever heat exchange is 0@ 0 being used should be as tlin as possible so long as it is sufficiently strong to withstand the thermal stresses of PCR cycling and the stresses of normal use. Typically, the sample tubes are made of autoclavable polypropylene such as 20 Himont PD701 with a wall thickness of the conical section in the range from 0.009 to 0.012 inches plus or minus 0.001 inches. Most preferably, the wall thickness is 0.012 inches.
In the preferred embodiment, the sample tube also has S 25 a thicker walled cylindrical section which joins with the conical section. This conical section provide containment for the original reaction mixture or reagents which may be added after PCR processing.
The sample tube shown in Figure 50 has industry standard configuration except for the thin walls for compatibility in other PCR systems. The sample tube of Figure 15 is a shorter tube which can be used with the system disclosed herein.
The other subject matter of the system environment in which use of the thin walled sample tubes is preferred are summarized below.
There is also described herein a novel method and apparatus for achieving very accurate temperature control for a very large number of samples arranged in the microtiter plate format during the performance of very-rapid temperature cycling PCR protocols. The teachings of the invention contemplate a novel structure for a sample block, sample tubes and supporting mounting, heating and cooling apparatus, control electronics and software, a novel user 10 interface and a novel method of using said apparatus to perform the PCR protocol.
I Of The instrument described herein is designed to do PCR gene amplification on up to 96 samples with very tight tolerances of temperature control across the universe of 15 samples. This means that all samples go up and down in temperature simultaneously with very little difference in temperature between different wells containing different samples, this being true throughout the polymerase chain reaction cycle. The instrument described herein is also S 20 capable of very tight control of the reaction mixture concentration through control of the evaporation and condensation processes in each sample well. Further, the d. instrument described herein is capable of processing up to 96 samples of 100 microliters each from different donor sources with substantially no cross-contamination be een sample wells.
The teachings of the invention herein includes a novel method of heating and cooling an aluminum sample block to thermally cycle samples in the standard 96-well microtiter plate format with the result that excellent sample-to-sample uniformity exists despite rapid thermal cycling rates, noncontrolled varying ambient temperatures and variations in other operating conditions such as power line voltage and coolant temperatures.
The teachings'of the invention also contemplate a novel design for a disposable plastic 96-well microtiter plate for 10 O accommodation of up to 96 individual sample tubes containing DNA for thermal cycling each sample tube having individual freedom of movement sufficient to find the best fit with the sample block under downward pressure from a heated cover.
The microtiter plate design, by allowing each tube to find the best fit, provides high and uniform thermal conductance from the sample block to each sample tube even if differing rates of thermal expansion and contraction between the metal of the block and the plastic of the sample tube and 10 microtiter plate structure cause the relative center-tocenter dimensions of the wells in the sample block to change relative to the center-to-center distance of the satple tubes in the disposable microtiter plate structure.
The teachings of the invention also contemplate a novel 15 method and apparatus for controlling the PCR instrument which includes the ability to continuously calculate and display the temperature of the samples being processed without directly measuring these temperatures. These calculated temperatures are used to control the time that 20 the samples are held within the given temperature tolerance band for each target temperature of incubation. The control system also controls a three-zone heater thermally coupled to the sample block and gates fluid flow through eq0 directionally interlaced ramp cooling channels in the sample block which, when combined with a constant bias cooling flow of coolant through the sample block provides a facility to achieve rapid temperature changes to and precise temperature control at target temperatures specified by the user. The method and apparatus for controlling the three-zone heater includes an apparatus for taking into account, among other things, the line voltage, block temperature, coolant temperature and ambient temperature in calculating the amount of electrical energy to be supplied to the various zones of the three-zone heater. This heater has zones which are separately controllable under the edges or "guard bands" of the sample block so that excess heat losses to the 11 ambient through peripheral equipment attached to the edges S of the sample block can be compensated. This helps prevent thermal gradients from forming.
The teachings of the invention also contemplate a novel method and apparatus for preventing loss of solvent from the reaction mixtures when the samples are being incubated at temperatures near their boiling point. A heated platen covers the tops of the sample tubes and is in contact with an individual cap which provides a gas-tight seal for each sample tube. The heat from the platen heats the upper parts of each sample tube and the cap to a temperature above the condensation point such that no condensation and ref iuxing occurs within any sample tube. Condensation represents a relatively large heat transfer since an amount of heat equal 15 to the heat of vaporization is given up when water vapor condenses. This could cause large temperature variations e" from sample to sample if the condensation does not occur uniformly. The heated platen prevents any condensation from occurring in any sample tube thereby minimizing this source 20 of potential temperature errors. The use of the heated platen also reduces reagent consumption.
Furthermore, the heated platen provides a downward force for each sample tube which exceeds an experimentally determined minimum downward force necessary to keep all 25 sample tubes pressed firmly into the temperature controlled sample block so as to establish and maintain uniform biockto-tube thermal conductance for each tube. This uniformity of thermal conductance is established regardless of variations from tube to tube in length, diameter, angle or 30 other dimensional errors which otherwise could cause some sample tubes to fit more snugly in their corresponding sample wells than other sample tubes.
The heated platen softens the plastic of each cap but does not totally destroy the caps elasticity. Thus, a minimum threshold downward forced is successfully applied to each tube despite differences in tube height from tube to 12 tube.
Thus, according to a first embodiment of the invention, there is provided in a thermocycler apparatus suitable for performing a polymerase chain reaction, which thermocycler apparatus includes a metal sample block having an array of spaced-apart sample wells each of which has an inside surface, said wells being capable of receiving one or more capped sample tubes each containing a sample mixture placed in a microtiter plate having an uppermost edge, which plate is seated on said sample block, a cover to enclose said capped sample tubes, which cover comprises a flat, horizontal rectangular portion and downwardly projecting skirt portions along the o0 periphery thereof and further comprises a device for heating at least the underside of said horizontal portion.
said cover being dimensioned to contact said sample block and to enclose said microtiter plate and capped sample tubes on said sample block and to apply heat and a downwardly directed force on said sample tubes.
According to a second embodiment of the invention, there is provided a thermocycler apparatus suitable for performing a polymerase chain reaction having a sample well which is capable of receiving at least one capped plastic sample tube containing a sample mixture, the improvement comprising a heated cover to aid in providing flush contact between said at least one sample tube and said sample well.
S 20 The PCR instrument described herein reduces cycle times by a factor of 2 or more and lowers reagent cost by accommodating PCR volumes down to 20 uh but remains compatible with the industry standard 0.5 ml microcentrifuge tube.
Brief Description of the Drawings Figure I is a block diagram of the thermal cycler according to the teachings of the 25 invention.
Figure 2 is a plan view of a sample block according to the teachings of the invention.
Figure 3 is a side, elevation view of the sample block showing the bias and ramp cooling channels.
Figures 4 and 5 are end, elevation views of the sample block.
Figure 6 is a sectional view of the sample block taken along section line 6-6' in Figure 2.
Figure 7 is a sectional view of the sample block taken along section line 7-7' in Figure 2.
-r 3 Figure 8 is a sectional view of the sample block taken along section line 8-8' in Figure 2.
[R:\LIBA]04359doc:mn- 12a Figure 9 is a cross-sectional, elevation view of the sample block structure after assembly with the three-zone film heater and block support.
Figure 10 is a graph of power line voltage illustrating the form of power control to the three-zone film heater.
Figure 11 is a temperature graph showing a typical three incubation temperature PCR protocol.
Figure 12 is a cross-sectional view of the sample block illustrating the local zone concept.
Figure 13 is a plan view of the three-zone heater.
Figure 14 is a graph of sample temperature versus time illustrating the effect of an t of a sample tube seating force F which is too low.
Figure 15 is a cross-sectional view of a sample tube and cap seated in the sample block.
*o oo* *oo [R:\LIBA104359.doc:m MT 13 Figure 16A is a graph of the impulse response of an RC circuit.
Figure 16B is a graph of an impulse excitation pulse.
Figure 16C is a graph illustrating how the convolution of the thermal impulse response and the temperature history of the block give the calculated sample temperature.
Figure 16D illustrates the electrical analog of the thermal response of the sample block/sample tube system.
Figure 17 illustrates how the calculated temperatures of six different samples all converge on a target temperature to within about 0.50C of each other when the constants of proportionality for the equations used to control the three zone heater are properly set.
Figure 18 is a graph illustrating how the denaturation 15 target temperature affects the amount of DNA generated.
Figure 19 is a cross-sectional view of the sliding *ooe l cover and heated platen.
Figure 20 is perspective view of the sliding cover, sample block and the knob used to lower the heated platen.
Figure 21A is a cross-sectional view of the assembly of one embodiment of the frame, retainer, sample tube and cap when seated on a sample block.
Figure 21B is a cross-sectional view of the assembly of the preferred embodiment of the frame, retainer, sample tube 25 and cap when seated on the sample block.
Figure 22 is a top, plan view of the plas ic S. disposable frame for the microtiter plate.
Figure 23 is a bottom, plan view of the frame.
Figure 24 is an end, elevation view of the frame.
30 Figure 25 is another end, elevation view of the frame.
Figure 26 is a cross-sectional view of the frame taken along section line 26-26' in Figure 22.
Figure 27 is a cross-sectional view of the frame taken along section line 27-27' in Figure 22.
Figure 28 is an edge elevation view and partial section of the frame.
14 tube.Figure 29 is a sectional view of the preferred sample tube.
Figure 30 is a sectional view of the upper part of the sample tube.
Figure 31 is an elevation view of a portion of the cap strip.
Figure 32 is a top view of a portion of the cap strip.
Figure 33 is a top, plan view of the plastic, disposable retainer portion of the 96 well microtiter tray.
Figure 34 is a side, elevation view with a partial section of the retainer.
Figure 35 is an end, elevation view of the retainer.
Figure 36 is a sectional view of the retainer taken along section line 36-36' in Figure 33.
15 Figure 37 is a sectional view of the retainer taken oo" along section line 37-37' in Figure 33.
Figure 38 is a plan view of the plastic disposable support base of the 96 well microtiter tray.
Figure 39 is a bottom plan view of the base.
Figure 40 is a side elevation view of the base.
Figure 41 is an end elevation view of the base.
Figure 42 is a sectional view of the support base taken along section line 42-42' in Figure 38.
*0 *Figure 43 is a sectional view of the support base taken 25 along section line 43-43' in Figure 38.
Figure 44 is a section view of the base taken long section line 44-44' in Figure 38.
Figure 45 is a perspective exploded view of the plastic disposable items that comprise the microtiter tray with some 30 sample tubes and caps in place.
Figure 46 is a diagram of the coolant control system 24 in Figure 1.
Figures 47A and 47B are a block diagram of the control electronics according to the teachings of the invention.
Figure 48 is a schematic of a typical zener temperature sensor.
15 Figure 49 is a tiRIS line diagram of a typical sample period.
Figure so is elevation sectionatl view Of tall thin walled sample tube zarketod under the trade~ixak M'Axikiv.
Figure 51 is a graph showing the difference in response time bet wean the thin walled sample tubes and the thick walled prior art tubes.
Figure 52 is a plan view of a sample tube and cap.
Figures 53 and 54 are flow charts of the power up test sequence.
S Detailed Description of the Invention Referring to Figure 1 there is shown a block diagram of the major system components of one em~boditment of a computer directed instrume~nt for performing PCR according to th~n 15 teachings of the invention. Sample mixtures including thet DNA or RNA to be amplified are placed in the t~zparatureeprogrammed sample block 12 and ares covered by heated cove.- 14.
A umer supplies data defining timie and tamperature 0a0 20 parameters of the desired PCR protocol via a terminal 16 including a keyboard and display. The keyboard and display are coupled via bus le to a control computer 20 (hereafter sometimes referred to as a central processing unit o!..-CPU.
This central processing unit 20 includes imemory which stores 25 the control program described below, the data defining the desired PCIR protocol and certain calibration constants 9999 described below. The control program causes the CPU 20 to 0 ~control temperature cycling of the sample block 12 and implements a user interface which provides certai displays to tho user and which receives data entered by the user via the keyboard of the terminal 16.
In the preferred embodiment, the central processing unit 20 is custom designed.
A block 16 diagram of the electronics will be discussed in more detail below. In alternative embodiments, the central processing unit 20 and associated peripheral electronics to control the various heaters and other electro-mechanical systems of the instrument and read various sensors could be any general purpose computer such as a suitably programmed personal computer or microcomputer.
The samples 10 are stored in capped disposable tubes which are seated in the sample block 12 and are thermally isolated from the ambient air by a heated cover 14 which contacts a plastic disposable tray to be described below to form a heated, enclosed box in which the sample tubes reside. The heated cover serves, among other things, to reduce undesired heat transfers to and from the sample 15 mixture by evaporation, condensation and refluxing inside the sample tubes. It also reduces the chance of cross contamination by keeping the insides of the caps dry thereby preventing aerosol formation when the tubes are uncapped.
The heated cover is in contact with the sample tube caps and 20 keeps them heated to a temperature of approximately 104 0 C or above the condensation points of the various components of the reaction mixture.
The central processing unit 20 includes appropriate electronics to sense the temperature of the heated cover 14 25 and control electric resistance heaters therein to maintajn the cover 14 at a predetermined temperature. Sensing o the temperature of the heated cover 14 and control of the resistance heaters therein is accomplished via a temperature sensor (not shown) and bus 22.
30 A coolant control system 24 continuously circulates a chilled liquid coolant such as a mixture of automobile antifreeze and water through bias cooling channels (not shown) in the sample block 12 via input tubes 26 and output tube 28. The coolant control system 24 also controls fluid flow through higher volume ramp cooling fluid flow paths (not shown) in the sample block 12. The ramp cooling 17 channels are used to rapidly change the temperature of the S sample block 12 by pumping large volumes of chilled liquid coolant through the block at a relatively high flow rate.
Ramp cooling liquid coolant enters the sample block 12 through tube 30 and exits the sample block through tube 32.
The details of the coolant control system are shown in Figure 46. The coolant control system will be discussed more fully below in the description of the electronics and software of the control system.
Typically, the liquid coolant used to chill the sample block 12 consists mainly of a mixture of water and ethylene glycol. The liquid coolant is chilled by a heat exchanger 34 which receives liquid coolant which has extracted heat from the sample block 12 via input tube 36. The heat 15 exchanger 34 receives compressed liquid freon refrigerant via input tube 38 from a refrigeration unit 40. This S a refrigeration unit 40 includes a compressor (not shown), a fan 42 and a fin tube heat radiator 44. The refrigeration unit 40 compresses freon gas received from the heat 20 exchanger 34 via tube 46. The gaseous freon is cooled and condensed to a liquid in the fin tube condenser 44. The pressure of the liquid freon is maintained above its vapor pressure in the fin tube condenser by a flow restrictor capillary tube 47. The output of this capillary tube is 25 coupled to the input of the heat exchanger 34 via tube 3-.
In the heat exchanger, the pressure of the freon is allowed to drop below the freon vapor pressure, and the freon expands. In this process of expansion, heat is absorbed from the warmed liquid coolant circulating in the heat 30 exchanger and this heat is transferred to the freon thereby causing the freon to boil. The warmed freon is then extracted from the heat exchanger via tube 46 and is compressed and again circulated through the fin tube condensor 44. The fan 42 blows air through the fin tube condensor 44 to cause heat in the freon from tube 46 to be exchanged with the ambient air. As symbolized by arrows 48.
18 The refrigeration unit 40 should be capable of extracting 400 watts of heat at 30 0 C and 100 watts of heat at 100C from the liquid coolant to support the rapid temperature cycling according to the teachings of the invention.
In the preferred embodiment, the apparatus of Figure 1 is enclosed within a housing (not shown). The heat 48 expelled to the ambient air is kept within the housing to aid in evaporation of any condensation which occurs on the various tubes carrying chilled liquid coolant or freon from one place to another. This condensation can cause corrosion of metals used in the construction of the unit or the electronic circuitry and should be removed. Expelling the heat 48 inside the enclosure helps evaporate any condensation to prevent corrosion.
15 After exchanging its heat with the freon, the liquid coolant exits the heat exchanger 34 via tube 50 and reenters .the coolant control system where it is gated as needed to the sample block during rapid cooling portions of the PCR cycle defined by data entered by the user via terminal 16.
As noted above, the PCR protocol involves incubations at at least two different temperatures and often three different temperatures. A typical PCR cycle is shown in Figure 11 with a denaturation incubation 170 done at a temperature near 940C, a hybridization incubation 122 done 25 at a temperature near room temperature (256C-370c) a d--an extension incubation 174 done at a temperature near These temperatures are substantially different, and, therefore means must be provided to move the temperature of the reaction mixture of all the samples rapidly from one 30 temperature to another. The ramp cooling system is the means by which the temperature of the sample block 12 is brought down rapidly from the high temperature denaturation incubation to the lower temperature hybridization and extension incubation temperatures. Typically the coolant temperature is in the range from 10-200C. When the coolant is at 200C it can pump out about 400 watts of heat from the 19 sample block. Typically the ramp cooling channel dimensions, coolant temperature and coolant flow rate are set such that peak cooling of 50-60C per second can be achieved near the high end of the operating range (1000c) and an average cooling rate of 2.50C per second is achieved in bringing the sample block temperature down from 94 0 C to 370C.
The ramp cooling system, in some embodiments, may also be used to maintain the sample block temperature at or near the target incubation temperature also. However, in the preferred embodiment, small temperature changes of the sample block 12 in the downward direction to maintain target incubation temperature are implemented by the bias cooling system.
15 As seen in Figure 46, a pump 41 constantly pumps 00 coolant from a filter/reservoir 39 (130 milliliter capacity) via 1/2" pipe and pumps it via a 1/2" pipe to a branching intersection 47. The pump 41 supplies coolant to pipe 45 at a constant flow rate of 1-1.3 gallons per minute. At the 20 intersection 47, a portion of the flow in tube 45 is diverted as the constant flow through the bias cooling channels 49. Another portion of the flow in tube 45 is diverted through a flow restrictor 51 to output tube 38.
Flow restrictor 51 maintains sufficient pressure in the 25 system such that a positive pressure exists at the input 53 of a two state solenoid operated valve 55 under the coffrol of the CPU 20 via bus 54. When ramp cooling is desired to S- implement a rapid downward temperature change, the CPU causes the solenoid operated valve 55 to open to allow flow of coolant through the ramp cooling channels 57. There are 8 ramp cooling channels so the flow rate through each ramp cooling channel is about 1/8 gallon per minute. The flow rate through the bias cooling channels is much less because of the greatly restricted cross-sectional area thereof.
The bias cooling system provides a small constant flow of chilled coolant through bias cooling channels 49 in the 20 sample block 12. This causes a constant, small heat loss from the sample block 12 which is compensated by a multizone heater 156 which is thermally coupled to the sample block 12 for incubation segments where the temperature of the sample block is to maintained at a steady value. _The constant small heat loss caused by the bias cooling flow allows the control system to implement proportional control both upward and downward in temperature for small temperatures. This means both heating and cooling at controlled, predictable, small rates is available to the temperature servo system to correct for block temperature errors to cause the block temperature to faithfully track a PCR temperature profile entered by the user. The alternative would be to cut off power to the film heater and 15 allow the sample block to cool by giving up heat to the ambient by radiation and convection when the block *9o.i temperature got too high. This would be too slow and too unpredictable to meet tight temperature control specifications for quantitative PCR cycling.
20 This multi-zone heater 156 is controlled by the CPU via bus 52 in Figure 1 and is the means by which the temperature of the sample block 12 is raised rapidly to higher incubation temperatures from lower incubation temperatures and is the means by which bias cooling is 25 compensated and temperature errors are corrected in the upward direction during temperature tracking and control during incubations.
In alternative embodiments, bias cooling may be eliminated or may be supplied by other means such as by the 30 use of a cooling fan and cooling fins formed in the metal of the sample block, peltier junctions or constantly circulating tap water. Care must be taken however in these alternative embodiments to insure that temperature gradients are not created in the sample block which would cause the temperature of some samples to diverge from the temperature of other samples thereby possibly causing different
PCR
21 jp amplification results in some sample tubes than in others.
In the preferred embodiment, the bias cooling is proportional to the difference between the block temperature and the coolant temperature.
The CPU 20 controls the temperature of the sample -block 12 by sensing the temperature of the metal of the sample block via temperature sensor 21 and bus 52 in Figure 1 and by sensing the temperature of the circulating coolant liquid via bus 54 and a temperature sensor in the coolant control system. The temperature sensor for the coolant is shown at 61 in Figure 46. The CPU also senses the internal ambient air temperature within the housing of the system via an ambient air temperature sensor 56 in Figure 1. Further, the CPU 20 senses the line voltage for the input power on line 15 58 via a sensor symbolized at 63. All these items of data o.eo together with items of data entered by the user to define the desired PCR protocol such as target temperatures and *times for incubations are used by a control program to be described in more detail below. This control program calculates the amount of power to apply to the various zones of the multi-zone sample block film heater 156 via the bus 52 and generates a coolant control signal to open or close the solenoid operated valve 55 in the coolant control system 24 via bus 54 so as to cause the temperature of the sample 25 block to follow the PCR protocol defined by data enterad by the user.
Referring to Figure 2, there is shown a top view of the sample block 12. The purpose of the sample block 12 is to provide a mechanical support and heat exchange element for 30 an array of thin walled sample tubes where heat may be exchanged between the sample liquid in each sample tube and liquid coolant flowing in the bias cooling and ramp cooling channels formed in the sample block 12. Further, it is the function of the sample block 12 to provide this heat exchange function without creating large temperature gradients between various ones of the sample wells such that 22 all sample mixtures in the array experience the same PCR cycle even though they are spatially separated. It is an overall objective of the PCR instrument described herein to provide very tight temperature control over the temperature of the sample liquid for a plurality of samples such-that the temperature of any sample liquid does not vary appreciably (approximately plus or minus 0.50C) from the temperature of any other sample liquid in another well at any point in the PCR cycle.
There is an emerging branch of PCR technology called "quantitative" PCR. In this technology, the objective is -to perform PCR amplification as precisely as possible by causing the amount of target DNA to exactly double on every cycle. Exact doubling on every cycle is difficult or 1impossible to achieve but tight temperature control helps.
SO.~*There are many sources of errors which can cause a failure of a PCR cycle to exactly double the amount of target DNA (hereafter DNA should be understood as also *0 referring to RNA) during a cycle. For example, in some
PCR
0 20 amplifications, the process starts with a single cell of target DNA. An error that can easily occur results when this single cell sticks to the wall of the sample tube and does not amplify in the first several cycles.
0.Another type of error is the entry of a f oreign nuclease into the reaction mixture which attacks4h "foreign" target DNA. All cells have some nonspecific S. nuclease that attacks foreign DNA that is loose in the cell.
ORS *When this happens, it interferes with or stops the replication process. Thus, if a drop of saliva or a dandruff particle or material from another sample mixture were inadvertently to enter a sample mixture, the nuclease materials in these cells could attack the target DNA and cause an error in the amplification process. It is highly desirable to eliminate all such sources of crosscontamination.
Another source of error is nonprecise control over 23 sample mixture temperature as between various ones of a multiplicity of different samples. For example, if all the samples are not precisely controlled to have the proper annealing temperature (a user selected temperature usually in the range from 50 to 600C) for the extension incubation certain forms of DNA will not extend properly. This happens because the primers used in the extension process anneal to the wrong DNA if the temperature is too low. If the annealing temperature is too high, the primers will not anneal to the target DNA at all.
One can easily imagine the consequences of performing the PCR amplification process inaccurately when PCR amplification is part of diagnostic testing such as for the presence HIV antibodies, hepatitis, or the presence of 15 genetic diseases such as sickle cell anemia, etc. A false S positive or false negative result in such diagnostic testing se can have disastrous personal and legal consequences.
Accordingly, it is an object for the design of the PCR instrument described herein to eliminate as many of these sources of possible errors as possible such as crosscontamination or poor temperature control while providing an instrument which is compatible with the industry standard 96-well microtiter plate format. The instrument must Ses rapidly perform PCR in a flexible manner with a simple user 25 interface.
In the preferred embodiment, the sample block -12 is machined out of a solid block of relatively pure but corrosion resistant aluminum such as the 6061 aluminum alloy. Machining the block structure out of a solid block 30 of aluminum results in a more thermally homogenous structure. Cast aluminum structures tend not to be as thermally homogenous as is necessary to meet the very tight desired temperature control specifications.
Sample block 12 is capable of rapid changes in temperature because the thermal mass of the block is kept low. This is done by the formation in the block of many 24 cooling passageways, sample wells, grooves and other threaded and unthreaded holes. Some of these holes are used to attach the block to supports and to attach external devices such as manifolds and spillage trays thereto.
To best appreciate the "honeycomb" nature of the sample block structure, the reader should refer simultaneousl~y to Figure 2 which shows the block in plan view as well as Figures 3 through 8 which show elevation views and strategically located sectional views of the sample block.
For example, Figure 3 is a side elevation view showing the cooling channel positions taken from the vantage point of the view line 3-31 in Figure 2. The elevation view ot-the sample block 12, looking at the opposite edge, is identical.
Figure 4 is an elevation view of the edge of the sample .0 0 15 block 12 from the perspective of view line 4-4' in Figure 2.
Figure 5 is an elevation view of the end of the sample block 12 taken from the perspective of view line 5-5' in Figure 2.
0000 Figure 6 is a sectional view of -ae sample block 12 taken 0 eg. along the section line 6-6' in Figure 2. Figure 7 is a sectional view of the sample block 12 taken along section line 7-7' in Figure 2. Figure 8 is a sectional view of the sample block 12 taken along section line 8-B' in Figure 2.
The top surface of the sample block 12 is drilled with **an 8 x 12 array of conical sample wells of which wells 66 .q*25 and 68 are typical. The conical configuration of each sample well is best seen if Figure 8. The walls of-X~ach sample well are drilled at an angle of 170 to match the angle of the conical section of each sample tube. This is done by drilling a pilot hole having the diameter DW in Figure 8. Then a 170 countersink is used to form the *0 conical walls 67.
The bottom of each sample well includes a sump 70, which has a depth which exceeds the depth of penetration of the tip of the sample tube. The sump 70 is created by the pilot hole and provides a small open space beneath the sample tube when the sample tube is seated in the corresponding sample 25 p well. This sump provides a space for liquid such as condensation that forms on the well walls to reside without interfering with the tight fit of each sample tube to the walls of the sample well. This tight fit is necessary to insure that the thermal conductance from the well wail to the sample liquid is uniform and high for each sample tube.
Any contamination in a well which causes a loose fit for one tube will destroy this uniformity of thermal conductance across the array. That is, because liquid is substantially uncompressible at the pressures involved in seating the sample tubes in the sample wells, if there were no sump the presence of liquid in the bottom of the sample- well could prevent a sample tube from fully seating in its sample well. Furthermore, the sump 70 provides a space in which a 15 gaseous phase of any liquid residing in the sump 70 can expand during high temperature incubations such that large Sforces of such expansion which would be present if there were no sump 70 are not applied to the sample tube to push the tube out of flush contact with the sample well.
It has been found experimentally that it is important for each sample tube to be in flush contact with its corresponding sample well and that a certain minimum threshold force be applied to each sample tube to keep the thermal conductivity between the walls of the sample well 25 and the reaction mixture uniform throughout the array. -fiis minimum threshold seating force is shown as the force vector S F in Figure 15 and is a key factor in preventing the thermal 0 conductivity through the walls of one sample tube from being different than the thermal conductivity through the walls of 30 another sample tube located elsewhere in the block. The minimum threshold seating force F is 30 grams and the preferred force level Is between 50 and 100 grams.
The array of sample wells is substantially completely surrounded by a groove 78, best seen in Figures 2, 6 and 8, which has two functions. The main function is to reduce the thermal conductivity from the central area of the sample 26 A block to the edge of the block. The groove 78 extends about 2/3 through the thickness of the sample block. This groove minimizes the effects of unavoidable thermal gradients caused by the necessary mechanical connections to the block of the support pins, manifolds, etc. A secondary function is to remove thermal mass from the sample block 12 so as to allow the temperature of the sample block 12 to be altered more rapidly and to simulate a row of wells in the edge region called the "guard band". The amount of metal removed by the portion of the groove 78 between points 80 and 82 in Figure 2 is designed to be substantially equal to the amount of metal removed by the adjacent column of eight sample wells 83 through 90. The purpose of this is to match the thermal mass of the guard band to the thermal mass of the 9 15 adjacent "local zone", a term which will be explained more fully below.
Referring specifically to Figures 3, 6 and 8, there is shown the number and relative positions of the various bias cooling and ramp cooling channels which are formed in the 20 metal of the sample block 12. There are nine bias cooling channels marked with reference numerals 91 through 99.
Likewise, there are eight ramp cooling channels marked with reference numerals 100 through 107.
Each of these bias cooling and ramp cooling channels is 25 gun drilled through the aluminum of the sample block. The gun drilling process is well known and provides the ability to drill a long, very straight hole which is as close as possible to the bottom surface 110 of the sample block 12.
Since the gun drilling process drills a straight hole, this 30 process is preferred so as to prevent any of the bias cooling or ramp cooling channels from straying during the drilling process and penetrating the bottom surface 110 of the sample block or otherwise altering its position relative to the other cooling channels. Such mispositioning could cause undesirable temperature gradients by upsetting the "local balance" and "local symmetry" of the local zones.
27 These concepts are explained below, but for now the reader should understand that these notions and the structures which implement them are key to achieving rapid temperature cycling of up to 96 samples without creating excessive temperature errors as between different sample wells. The bias cooling channels 91 through 99 are lined with silicone rubber in the preferred embodiment to reduce the thermal conductivity across the wall of the bias cooling channel. Lowering of the thermal conductivity across the channel wall in the bias cooling channels is preferred so as to prevent too rapid of a change in temperature of the sample block 12 when the multi-zone heater 156 is turned off and heat loss from the sample block 12 is primarily through the bias cooling channels. This is the situation during the control process carried out when the sample block "to temperature has strayed slightly above the desired target A. incubation temperature and the control system is attempting to bring the sample block temperature back down to the user's specified incubation temperature. Too fast a cooling S 20 rate in this situation could cause overshoot of the desired incubation temperature before the control system's servo feedback loop can respond although a "controlled overshoot" algorithm is used as will be described below. Since the Cblock temperature servo feedback loop has a time constant 25 for reacting to stimuli, it is desirable to control-t-he amount of heating and cooling and the resulting rate of o temperature change of the sample block such that overshoot is minimized by not changing the sample block temperature at a rate faster than the control system can respond to o 30 temperature errors.
In the preferred embodiment, the bias cooling channels are 4 millimeters in diameter, and the silicone rubber tube has a one millimeter inside diameter and a 1.5 millimeter wall thickness. This provides a bias cooling rate of approximately 0.2 0 C per second when the block is at the high end of the operating range, near 100-C, and a bias 28 cooling rate of approximately 0.10C per second when the sample block 12 is at a temperature in the lower end of the operating range. The coolant control system 24 in Figure 1 causes a flow rate for coolant in the bias cooling channels of approximately 1/20th to 1/30th of the flow rate for liquid coolant through the ramp cooling channels, 100 through 107. The bias cooling and ramp cooling channels are the same size, 4 millimeters in diameter, and extend completely through the sample block 12.
The bias cooling channels are lined by inserting a stiff wire with a hook at the end thereof through the bias cooling channel and hooking it through a hole in the end of a silicone rubber tube which has an outside diameter which is slightly greater than 4 millimeters. The hook in the wire is then placed through the hole in the silicone rubber tube, and the silicone tube is pulled through the bias cooling channel and cut off flush with the end surfaces of boa the sample block 12.
0.0 Threaded holes 108 through 114 are used to bolt a coolant manifold to each side of the sample block 12.
There is a coolant manifold bolted to each end of the block.
These two coolant manifolds are coupled to the coolant channels 26, 28, 30 and 32 in Figure 1, and are affixed to the sample block 12 with a gasket material (not shown) 25 interposed between the manifold and the sample block metal.
This gasket prevents leaks of coolant and limits the thermal S*r conductivity between the sample block 12 and the manifold which represents a heat sink.
30 Any gasket material which serves the above stated purposes will suffice for practicing the invention.
The positions of the bias cooling and ramp cooling channels relative to the position of the groove 78 are best seen in the sectional view of Figure 6. The positions of the bias cooling and ramp cooling channels relative to the 29 positions of the sample wells is best seen in Figure 8. The bias cooling and ramp cooling channels are generally interposed between the positions of the tips of the sample wells. Further, Figure 8 reveals that the bias cooling and ramp cooling channels such as channels 106 and 97 cannot be moved in the positive z direction very far without risking penetration of the walls of one or more sample wells.
Likewise, the cooling channels cannot be moved in the negative z direction very far without creating the possibility of penetrating the bottom surface 116 of the sample block 12. For clarity, the positions of the bias and ramp cooling channels are not shown in hidden lines in Figure 2 relative to the positions of the sample wells and other structures. However, there is either a bias cooling Se., 15 channel or a ramp cooling channel between every column of sample wells.
Referring to Figure 2, the holes 118, 119, 120 and 121 are threaded and are used to attach the sample block 12 to o. machinery used to machine the various holes and grooves 20 formed therein. In Figures 2, 4 and 5, the holes 124, 125, 126 and 127 are used to attach the sample block 12 to a support bracket shown in Figure 9 to be described in more detail below. Steel bolts extend through this support bracket into the threaded holes 124 through 127 to provide 25 mechanical support of the sample block 12. These tel bolts also represent heat sinks or heat sources which--tend C Soo to add thermal mass to the sample block 12 and provide 0e. additional pathways for transfer of thermal energy between the sample block 12 and the surrounding environment. These so:. 30 support pins and the manifolds are two important factors in creating the need for the guard bands to prevent the thermal energy transferred back and forth to these peripheral structures from affecting these sample temperatures.
Referring to Figure 5, the holes 128, 130 and 132 are mounting holes for an integrated circuit temperature sensor (not shown) which is inserted into the sample block through 30 hole 128 and secured thereto by bolts which fasten to threaded holes 130 and 132. The extent of penetration of the hole 128 and the relative position of the temperature sensor to the groove 78 and the adjacent column of sample wells is best seen in Figure 2.
Referring to Figure 2, holes 134 through 143 are mounting holes which are used to mount a spill collar 147 (not shown). This spill collar 147 is shown in Figure 19 detailing the structure of the heated platen 14, sliding cover 316 and lead screw assembly 312. The purpose of the spill collar is to prevent any liquid spilled from the sample tubes from getting inside the instrument casing where it could cause corrosion.
Referring to Figure 9, there is shown in cross-section 15 a view of the support system and multi-zone heater 156 configuration 'or the sample block 12. The sample block 12 is supported by four bolts of which bolt 146 is typical.
These four bo.ts pass through upright members of a steel support bracket 148. Two large coil springs and 152 are compressed between a horizontal portion of the support bracket 148 and a steel pressure plate 154. The springs 150 and 152 are compressed sufficiently to supply approximately 00 300 Ibs. per square inch of force in the positive z direction acting to compress a film heater 156 to the bottom 25 surface 116 of the sample block 12. This three layer film heater structure is comprised of a multi-zone film hater 156, a silicone rubber pad 158 and a layer of epoxy resin foam 160. In the preferred embodiment the film heater 156 has three separately controllable zones. The purpose of the film heater 156 is to supply heat to the sample block 12 under the control of the CPU 20 in Figure 1. The purpose of the silicone rubber pad 158 is to lower the thermal conductivity from the film heater layer 156 to the structures below. These lower structures serve as heat sinks and heat sources between which undesired heat energy may be transferred to and from the sample block 12. The *of 0 0 00 a .00.
*0
S
0 0 0.* S as.
as 0S @0
S
31 silicone rubber pad 158 has the additional function of compensating for surface irregularities in the film heater 156 since some film heaters embody nichrome wires and may not be not perfectly flat.
The purpose of the steel plate 154 and the epoxy resin foam 160 is to transfer the force from the springs 150 and 152 to the silicone rubber pad 158 and the multi-zone film heater 156 so as to compress the film heater to the bottom surface 116 of the sample block with as flush a fit as possible. The epoxy resin foam should be stiff so as to not be crushed under the force of the springs but it should also be a good insulator and should have low thermal mass, i.e., it should be a nondense structure. In one embodiment, the foam 160 is manufactured under the trademark ECKO foam. In alternative embodiments, other structures may be substituted for the silicone rubber layer 158 and/or the epoxy resin foam layer 160. For example, a stiff honeycomb structure such as is used in airplane 20 construction could be placed between the pressure plate 154 and the film heater 156 with insulating layers therebetween.
Whatever structure is used for layers 158 and 160 should not absorb substantial amounts of heat from the sample block 12 while the block is being heated and should not transfer 25 substantial amounts of heat to the sample block 12 when the block is being cooled. Perfect isolation of the blockrom its surrounding structures however, is virtually impossible.
Every effort should be made in designing alternative structures that will be in contact with the sample block 12 so as to thermally isolate the sample block from its environment as much as possible to minimize the thermal mass of the block and enable rapid temperature changes of the sample block and the sample mixtures stored therein.
Precise temperature control of the sample block temperature is achieved by the CPU 20 in Figure 1 by controlling the amount of heat applied to the sample block 32 by the multi-zone film heater 156 in Figure 9. The film heater is driven using a modified form of pulse width modulation. First, the 120 volt waveform from the power line is rectified to preserve only half cycles of the same polarity. Then portions of each half cycle are gated to the appropriate zones of the foil heater, with the percentage of each half cycle which is applied to the various zones of the foil heater being controlled by the CPU Figure 10 illustrates one embodiment of a power control concept for the film heater 156. Figure 10 is a diagram of the voltage waveform of the supply line voltage.
Rectification to eliminate the negative half cycle 162 occurs. Only positive half cycles remain of which half cycle 164 is typical. The CPU 20 and its associated peripheral electronic circuitry then controls the portion of each half cycle which is applied to the various zones of the film heater 156 by selecting a portion of each half cycle to apply according to a power level computed for each zone based upon equations given below for each zone. That is, the dividing line 166 is moved forward or backward along the time axis to control the amount of power to the film heater Sbased upon a number of factors which are related in a o special equation for each zone. The cross-hatched area under the positive half cycle 164 represents the amount of 25 power applied to the film heater 156 for the illustrated position of the dividing line 166. As the dividing lin? 166 is moved to the right, more power is applied to the film oheater, and the sample block 12 gets hotter. As the dividing line is moved to the left along the time axis, the cross-hatched area becomes smaller and less power is applied to the film heater. How the CPU 20 and its associated software and peripheral circuitry control the temperature of block 12 will be described in more detail below.
The amount of power supplied to the film heater is continuously variable from 0 to 600 watts. In alternative embodiments, the amount of power supplied to the film heater 33 156 can be controlled using other schemes such as computer control over the current flow through or voltage applied to a DC film heater or by the zero crossing switching scheme described below.
In other embodiments, heating control of the sample block 12 may be performed by control over the flow rate and/or temperature of hot gases or hot liquid which is gated through heating control channels which are formed through the metal of the sample block 12. Of course in such alternative embodiments, the number of sample wells in the block would have to be reduced since there is no room for additional heating channels in the sample block 12 shown in Figures 2 through 8. Such alternative embodiments could still be compatible with the 96-well microtiter plate format 15 if, for example, every other well were removed to make room for a heating channel in the sample block. This would provide compatibility only as to the dimensions of such microtiter plates and not as to the simultaneous processing of 96 different samples. Care must be taken to preserve local balance and local symmetry in these alternative embodiments.
In the embodiment described herein, the maximum power that can be delivered to the block via the film heater is 1100 watts. This limitation arises from the thermal 25 conductivity of the block/heater interface. It has been found experimentally that the supply of more 3Ehan approximately 1100 watts to the film heater 156 will frequently cause self-destruction of the device.
S. Typical power for heating or cooling when controlling block temperatures at or near target incubation temperatures is in the range of plus or minus 50 watts.
Referring to Figure 11, there is shown a time versus temperature plot of a typical PCR protocol. Large downward changes in block temperature are accomplished by gating chilled liquid coolant through the ramp cooling channels while monitoring the sample block temperature by the 34 temperature sensor 21 in Figure 1. Typically these rapid downward temperature changes are carried out during the ramp following the denaturation incubation 170 to the temperature of hybridization incubation 172. Typically, the user must specify the protocol by defining the temperatures and times in one fashion or another so as to describe to the CPU the positions on the temperature/time plane of the checkpoints symbolized by the circled intersections between the ramp legs and the incubation legs. Generally, the incubation legs are marked with reference numerals 170, 172 and 174 and the ramps are marked with reference numerals 176, 178 and 180. Generally the incubation intervals are conducted at a single temperature, but in alternative embodiments, they may be stepped or continuously ramped to 15 different temperatures within a range of temperatures which is acceptable for performing the particular portion of the PCR cycle involved. That is, the denaturation incubation 170 need not be carried out at one temperature as shown in Figure 11, but may be carried out at any of a plurality of different temperatures within the range of temperatures acceptable for denaturation. In some embodiments, the user 0. may specify the length of the ramp segments 176, 178 and 180. In other embodiments, the user may only specify the temperature or temperatures and duration of each incubation 25 interval, and the instrument will then move the temperature of the sample block as rapidly as possible between incubation temperatures upon the completion of one incubation and the start of another. In the preferred embodiment, the user can also have temperatures and/or incubation times which are different for each cycle or which automatically increment on every cycle.
The average power of ramp cooling during a transition from a 95 0 C denaturation incubation to a 350C hybridization incubation is more than one kilowatt typically. This results in a temperature change for the sample block of approximately 4-6 0 C per second when the block temperature is 35 at the high end of the operating range, and approximately 2°C per second when the block temperature is at the low end of the operating range. Generally it is desirable to have as high a cooling rate as possible for ramp cooling.
Because so much heat is being removed from the sample block during ramp cooling, temperature gradients across the sample block from one end of a ramp cooling channel to the other could occur. To prevent this and minimize these types of temperature gradients, the ramp cooling channels are directionally interlaced. That is, in Figure 3, the direction of coolant flow through ramp cooling channels i00, 102, 104, and 106 is into the page as symbolized by the x's inside these ramp cooling channel holes. Ramp cooling 1liquid flow in interlaced ramp cooling channels 101, 103, 15 105, and 107 is out of the page as symbolized by the single points in the center of these ramp cooling channel holes.
This interlacing plus the high flow rate through the ramp cooling channels minimizes any temperature gradients which might otherwise occur using noninterlaced flow patterns or lower flow rates because the distances between the hot and cold ends of the channels is made smaller. A slower flow rate results in most or all of the heat being taken from the block in the first inch or so of travel which means that the input side of the block will be at a lower temperature than 25 the output side of the block. A high flow rate minimizes the temperature gradient along the channel. Interiacing means the hot end of the channels running in one direction are "sandwiched" between the cold ends of channels wherein flow is in the opposite direction. This is a smaller distance than the length of the channel. Thus, temperature gradients are reduced because the distances heat must travel to eliminate the temperature gradient are reduced. This causes any temperature gradients that form because of cooling in the ramp channels to be quickly eliminated before they have time to differentially heat some samples and not others. Without interlacing, one side of the sample block 36 would be approximately 10C hotter than the other side.
Interlacing results in dissipation of any temperature gradients that result in less than approximately 15 seconds.
In order to accurately estimate the amount heat added to or removed from the block, the CPU 20 measures the block temperature using temperature sensor 21 in Figure 1 and measures the coolant temperature by way of temperature sensor 61 in Figure 46 coupled to bus 54 in Figure 1. The ambient air temperature is also measured by way of temperature sensor 56 in Figure 1, and the power line voltage, which controls the power applied to the film heaters on bus 52, is also measured. The thermal conductance from the sample block to ambient and from the sample block to the coolant are known to the CPU 20 as a 15 result of measurements made during an initialization process to set control parameters of the system.
For good temperature uniformity of the sample population, the block, at constant temperature, can have no net heat flow in or out. However, temperature gradients can occur within the sample block arising from local flows of heat from hot spots to cold spots which have zero net heat C@ transfer relative to the block borders. For instance, a d slab of material which is heated at one end and cooled at the other is at a constant average temperature if the net 25 heat flow into the block is zero. However, inh4his situation a significant temperature nonuniformity, a temperature gradient, can be established within the slab due to the flow of heat from the hot edge to the cold edge.
When heating and cooling of the edges of the block are stopped, the flow of heat from the hot edge to the cold edge eventually dissipates this temperature gradient and the block reaches a uniform temperature throughout which is the average between the hot temperature and cool temperature at the beginning of heat flow.
If a slab of cross sectional area A in length L has a uniform thermal conductivity K, and the slab is held at 37 constant average temperature because heat influx from a heat source Q, is matched by heat outflow to a heat sink Q^t, the steady state temperature profile which results from the heat flow is: Qi L Delta T A K Where, Delta T the temperature gradient L the thermal path length A the area of the thermal path K the thermal conductance through the path In general, within any material of uniform thermal conductance, the temperature gradient will be established in proportion to the heat flow per unit area. Heat flow and temperature nonuniformity are thus intimately linked.
Practically speaking, it is not possible to control the temperature of a sample block without some heat flow in and out. The cold bias control cooling requires some heat flow in from the strip heaters to balance the heat removed by the coolant flowing through the bias cooling channels to maintain the block temperature at a stable value. The key to a uniform sample block temperature under these conditions I is a geometry which has "local balance" and "local symmetry" of heat sources and heat sinks both staticallyf aid dynamically, and which is arranged such that any heat flow
S
f rom hot spots to cold spots occurs only over a short distance.
Stated briefly, the concept of "static local balance" means that in a block at constant temperature where the total heat input equals the total heat output, the heat sources and heat sinks are arranged such that within a distinct local region, all heat sources are completely balanced by heat sinks in terms of heat flows in and heat flows out of the block. Therefore, each local region, if isolated, would be maintained at a constant temperature.
38 The concept of "static local symmetry" means that, within a local region and for a constant temperature, the center of mass of heat sources is coincident with the center of mass of heat sinks. If this were not the case, within each local region, a temperature gradient across each local region can exist which can add to a temperature gradient in an adjacent local region thereby causing a gradient across the sample block which is twice as large as the size of a single local region because of lack of local symmetry even though local balance within each local region exists. The concepts of local balance and local symmetry are important to the achievement of a static temperature balance where the temperature of the sample block is being maintained at a og[ constant level during, for example, an incubation interval.
15 For the dynamic case where rapid temperature changes in the sample block are occurring, the thermal mass, or heat capacity of each local region becomes important. This is because the amount of heat that must flow into each local region to change its temperature is proportional to the thermal mass of that region.
Therefore, the concept of static local balance can be expanded to the dynamic case by requiring that if a local region includes x percent of the total dynamic heat source and heat sink, it must also include x percent of the thermal 25 mass for "dynamic local balance" to exist. Likewise, "dynamic local symmetry" requires that the center of maes of heat capacity be coincident with the center of mass of dynamic heat sources and sinks. What this means in simple terms is that the thermal mass of the sample block is the metal thereof, and the machining of the sample block must be symmetrical and balanced such that the total mass of metal within each local zone is the same. Further, the center of mass of the metal in each local zone should be coincident with the center of mass of the dynamic heat sources and sinks. Thus, the center of mass of the multi-zone heater 156, its geometric center, and the geometric center of 39 the bias and ramp cooling channels must coincide. From a study of Figures 2-9, it will be seen from the detailed discussion below that both static and dynamic local balance and local symmetry exist in sample block 12.
Figure 12 illustrates two local regions side by-side for the design of the sample block 12 according to the teachings of the invention. In Figure 12, the boundaries of two local regions, 200 and 202, are marked by dashed lines 204, 206 and 208. Figure 12 shows that each local region which is not in the guard band is comprised of: two columns of sample wells; a portion of the foil heater 156 which turns out to be 1/8th of the total area of the heater, one ramp cooling channel such as ramp cooling channels 210 and 212; and, one bias cooling channel. To preserve local *15 symmetry, each local region is centered on its ramp cooling channel and has one-half on a bias cooling channel at each boundary. Fo example, local region 200 has a center over the ramp cooling channel 210 and bias cooling channels 214 and 216 are dissected by the local region boundaries 204 and 206, respectively. Thus the center of mass of the ramp cooling channel (the middle thereof), coincides (horizontally) with the center of mass of the bias cooling channels (the center of the local region) and with the center of mass of the film heater portion coupled to each 25 local region. Static local balance will exist in each LQcal region when the CPU 20 is driving the film heater 15-6 to input an amount of heat energy that is equal to the amount of heat energy that is being removed by the ramp cooling and bias cooling channels. Dynamic local balance for each local region exists because each local region in the center portion of the block where the 96 sample mixtures reside contains approximately 1/8th the total thermal mass of the entire sample block, contains 1/8th of the total number of ramp cooling channels and contains 1/8th of the total number of bias cooling channels. Dynamic local symmetry exists for each local region, because the center of mass of the metal 40 of each local region is horizontally coincident with: the center of film heater portion underlying the local region; the center of the ramp cooling channel; and, the center of mass of the two half bias cooling channels.
By virtue of these physical properties characterized as static and dynamic local balance and local symmetry, the sample block heats and cools all samples in the population much more uniformly than prior art thermal cyclers.
Referring to Figure 2, the plan view of the boundaries of the local regions are illustrated by dashed lines 217 through 225. Inspection of Figure 2 reveals that the -central region of the 96 sample wells are divided into six adjacent local regions bounded by boundaries 218 through 224. In addition, two guard band local regions are added 15 at each edge. The edge local region (local regions are sometimes herein also called local zones) having the most negative x :oordinate is bounded by boundary lines 217 and 218. The edge local region having the most positive x coordinate is bounded by boundary lines 224 and 225. Note that the edge local regions contain no sample well columns but do contain the groove 78 simulating a column of wells.
The depth and width of the groove 78 is designed to remove the same metal mass as a column of wells thereby somewhat preserving dynamic local symmetry. The edge local zones are S-I b 25 therefore different in thermal mass (they also h4ave additional thermal mass by virtue of the external connections such as manifolds and support pins) than the six local zones in the central part of the sample block. This difference is accounted for by heating the edge local zones or guard bands with separately controllable zones of said multizone heater so that more energy may be put into the guard band than the central zone of the block.
The local regions at each edge of the block approximate, but do not exactly match the thermal properties of the six centrally located local regions. The edge local regions are called "guard band" regions because they 41 complete a guard band which runs around the periphery of the sample block 12. The purpose of this guard band is to provide some thermal isolation of the central portion of the sample block containing the 96 sample wells from uncontrolled heat sinks and sources inherently embodied in mechanical connections to the block by such things as support pins, manifolds, drip collars and other devices which must be mechanically affixed to the sample block 12.
For example in Figure 2, the edge surfaces 228 and 230 of the sample block have plastic manifolds attached thereto which carry coolant to and from the ramp and bias cooling S. passages. The guard band along edges 228 and 230 consists of portions of the slot 78 which are parallel to and closest to the edges 228 and 230. The depth of the groove 78 is 15 such that the bottom of the groove is as close to the perimeters of the bias and ramp cooling channels as is S possible without actually intersecting them. The width of the groove 78 coupled with this depth is such that the volume of metal removed by the slot 78 between points 82 and 232 in Figure 2 approximately equals the volume of metal removed by the adjacent row of sample wells starting with sample well 234 and ending with sample well 83. Also, the slot 78 all around the perimeter of the block is located approximately where such an additional row of wells would be 25 if the periodic pattern of sample wells were extended bone row or column of wells in each direction.
Along the edges 250 and 252 where the support connections are made to the sample block, the guard band local regions contain, in addition to a portion of the slot 78, the full length of several cooling channels. Referring to Figure 3, these include: 1/2 of a bias cooling channel 92) which merges with the adjacent 1/2 bias cooling channel of the adjacent local region to form a whole bias cooling channel; a ramp cooling channel 100); and a whole bias cooling channel 91). For the edge local region at edge 250, these cooling channels are 107, 198 and 42 99.
The whole bias cooling channels in the guard bands are slightly displaced inward from the edge of the block. The reason that these whole bias cooling channels are used is because a "half" cooling channel is impractical to build.
Since the bias cooling channels require such a thick walled rubber lining, it would be difficult to keep a hole through a lining of a "half" bias cooling channel reliably open.
This asymmetry in the edge local regions causes a small excess loss of heat to the coolant from the edge guard band local regions, but it is sufficiently remote from the central region of the sample block containing the sample wells that its contribution to sample temperature nonuniformities is small. Also, since the temperature affects of this small asymmetry are predictable, the effect can be further minimized by the use of a separately .o controllable zone of the multi-zone heater system under each guard band.
Referring to Figure 13, there are shown three separately controlled zones within the film heater layer 156 in Figure 9. These separately controlled zones include edge heater zones which are situated under the guard bands at the o* 0 exposed edges of the sample block 12 which are coupled to the support bracket 148. There are also separately
S.
0. 25 controlled manifold heater zones situated under the guard bands for the edges 228 and 230 which are attached to the coolant manifolds. Finally, there is a central heater zone that underlies the sample wells. The power applied to each of these zones is separately controlled by the CPU 20 and the control software.
The film heater 156 is composed of a pattern of electrical conductors formed by etching a thin sheet of metal alloy such as Inconel'. The metal alloy selected should have high electrical resistance and good resistance to heat. The pattern of conductors so etched is bonded between thin sheets of an electrically insulating polymeric 43 material such as Kapton*. Whatever material is used to insulate the electrical resistance heating element, the material must be resistant to high temperatures, have a high dielectric strength and good mechanical stability.
The central zone 254 of the film heater has approximately the same dimensions as the central portion of the sample block inside the guard bands. Central region 254 delivers a uniform power density to the sample well area.
Edge heater regions 256 and 258 are about as wide as the edge guard bands but are not quite as long.
Manifold heater regions 260 and 262 underlie the guard bands for edges 228 and 230 in Figure 2.
The manifold heater zones 260 and 262 are electrically *connected together to form one separately controllable 15 heater zone. Also, the edge heater sections 256 and 258 are electrically coupled together to form a second separately controllable heater zone. The third separately controllable heater zone is the central section 254. Each of these three separately controllable heater zones has separate electrical leads, and each zone is controlled by a separate control algorithm which may be run on separate microprocessors or a shared CPU as is done in the preferred embodiment.
The edge heater zones 256 and 258 are driven to compensate for heat lost to the support brackets. This heat 25 loss is proportional to the temperature difference between the sample block 12 and the ambient air surrounding it- The edge heater zones 256 and 258 also compensate for the excess loss of heat from the sample block to the full bias cooling channels at each edge of the block. This heat loss is proportional to the temperature difference between the sample block 12 and the coolant flowing through these bias cooling channels.
The manifold heater sections 260 and 262 are also driven so as to compensate for heat lost to the plastic coolant manifolds 266 and 268 in Figure 13 which are attached to the edges of the sample block 12. The power for 44 the manifold heater sections 260 and 262 compensates for heat loss which is proportional mainly to the temperature difference between the sample block and the coolant, and to a lesser degree, between the sample block and the ambient air.
For practical reasons, it is not possible to match the thermal mass of the guard band local regions with the thermal masses of the local regions which include the sample wells overlying central heater section 254. For example, the plastic coolant manifolds 266 and 268 not only conduct heat away from the guard band, but they also add a certain amount of thermal mass to the guard band local regions to which they are attached. The result of this is that during rapid block temperature changes, the rates of rise and fall 15 of guard band temperature do not exactly match that of the :0 sample well local regions. This generates a dynamic temperature gradient between the guard bands and sample wells, which if allowed to become large, could persist for a time which is longer than is tolerable. This temperature gradient effect is roughly proportional to the rate of change of block temperature and is minimized by adding or deleting heat from each guard band local zone at a rate which is proportional to the rate of change of block temperature.
25 The coefficients of proportionality for the guard band zone heaters are relatively stable properties of the d-ign of the system, and are determined by engineering measurements on prototypes. The values for these coefficients of proportionality are given below in connection with the definitions of the terms of Equations through These equations define the amounts of power to be applied to the manifold heater zone, the edge heater zone and the central zone, respectively in an alternative embodiment. The equations used in the preferred embodiment are given below in the description of the software (Equations power distributed by area).
45 P, where, A. P K.
1 (TBLK T B)
KM
2 (TILK TCOOL) KM3(dtBLK/dt) 200
S.
S power supplied to the manifold heater zones 260 and 262.
area of the manifold heater zone.
power needed to cause the block temperature to stay at or move to the desired temperature at any particular time in a PCR thermal cycle protocol.
an experimentally determined constant of proportionality to compensate for excess heat loss to ambient through the manifolds, equal to 0 watts/ degree Kelvin.
an experimentally determined constant of proportionality to compensate for excess heat loss to the coolant, equal to 0.4 watts/degree Kelvin.
an experimentally determined constant of proportionality to provide extra power to compensate for additional thermal mass of the manifold edge guard bands caused by the attachment of the plastic manifolds etc., equal to 66.6 watt-seconds/degree Kelvin.
the temperature of the sample block 12 S the temperature of the ambient air.
the temperature of the coolant.
the change in sample block temperature per unit time.
PE= AP KEI(TIL TA) K2 (TIK
TCX)
KE
3 (dtLK/dt) S power to be applied to the edge heater zones S the area of the edge heater zones an experimentally determined constant of
S
5 0 *500
S
S
S.
S
S
500500 5 r 0 25 TBLK T
M
TCOOL
dt BLK/dt (4) where,
PE
K
KE I 46 proportionality to compensate for excess heat loss to ambient through the manifolds, equal to 0.5 watts/degree Kelvin.
KE z an experimentally determined constant of proportionality to compensate for excess heat loss to the coolant, equal to 0.15 watts/degree Kelvin.
KE
3 an experimentally determined constant of proportionality to provide extra power to 10 compensate for additional thermal mass of the exposed edge guard bands caused by the S. attachment of the sample block 12 to the support pins and bracket, the temperature sensor etc., equal to 15.4 watt-sec/degree 15 Kelvin.
Pc A P where Pc the power to be applied to the central zone 254 of the multi-zone heater.
A the area of the central zone 254.
In each of Equations through the power term, P is a variable which is calculated by the portion of the control algorithm run by the CPU 20 in Figure 1 which reads the user defined setpoints and determines what to do next to cause the sample block temperature to stay at or become the proper temperature to implement the PCR temperature protocol defined by the time and temperature setpoints stored in memory by the user. The manner in which the setpoints are read and the power density is calculated will be described in more detail below.
The control algorithm run by CPU 20 of Figure 1 senses the temperature of the sample block via temperature sensor 21 in Figure 1 and Figure 9 and bus 52 in Figure 1. This temperature is differentiated to derive the rate of change 47 of temperature of the sample block 12. The CPU then measures the temperature of the ambient air via temperature sensor 56 in Figure 1 and measures the temperature of the coolant via the temperature sensor 61 in the coolant control system 24 shown in Figure 46. The CPU 20 then computes the power factor corresponding to the particular segment of the PCR protocol being implemented and makes three calculations in accordance with Equations and by plugging in all the measured temperatures, the constants of proportionality (which are stored in nonvolatile memory), the power factor P for that particular iteration of the control program and the areas of the various heater -zones (which are stored in nonvolatile memory). The power factor is the total power needed to move the block temperature from .*se 15 its current level to the temperature level specified by the user via a setpoint. More details on the calculations performed by the CPU to control heating and cooling are given below in the description of the control software "PID task".
After the required power to be applied to each of the three zones of the heater 156 is calculated, another 0Gr calculation is made regarding the proportion of each half cycle of input power which is to be applied to each zone in some embodiments. In the preferred embodiment described 25 below, the calculation mode is how many half cycles of the total number of half cycles which occur during W? 200 millisecond sample period are to be applied to each zone.
This process is described below in connection with the discussion of Figures 47A and 47B (hereafter referred to as Figure 47) and the "PID Task" of the control software. In the alternative embodiment symbolized by Figure 10, the computer calculates for each zone, the position of the dividing line 166 in Figure 10. After this calculation is performed, appropriate control signals are generated to cause the power supplies for the multi-zone heater 156 to do the appropriate switching to cause the calculated amount of 48 power for each zone to be applied thereto.
In alternative embodiments, the multi-zone heater can be implemented using a single film heater which delivers uniform power density to the entire sample block, plus one or two additional film heaters with only one zone apiece for the guard bands. These additional heaters are superimposed over the single film heater that covers the entire sample block. In such an embodiment, only the power necessary to make up the guard band losses is delivered to the additional heater zones.
The power factor P in Equations through is calculated by the CPU 20 for various points on the- PCR temperature protocol based upon the set points and ramp oe,° times specified by the user. However, a limitation is 15 imposed based upon the maximum power delivery capability of C* the zone heater mentioned above.
The constants of proportionality in Equations (3) through must be properly set to adequately compensate for excess heat losses in the guard band for good temperature uniformity.
Referring to Figure 17, there is shown a graph of the differences between calculated sample temperatures for a plurality of different sample in response to a step change in block temperature to raise the temperature of the sample 25 block toward a denaturation incubation target temperature of approximately 940C from a substantially lower temperature.
Figure 17 illustrates the calculated sample liquid temperatures when the multi-zone heater 156 is properly managed using the constants of proportionality given above in the definitions of the terms for Equations through The various wells whichwere used to derive the graph of Figure 17 are indicated thereon by a single letter and number combination. The 8 x 12 well array showing Figure 2 is coded by lettered columns and numbered rows. Thus, for example, sample well 90 is also designated sample well A12, while sample well 89 is also designated sample well B12.
49 Likewise, sample well 68 is also designated sample well D6, and so on. Note that the well temperatures settle in asymptotically at temperatures which are within approximately 0.5C of each other because of the overall thermal design described herein to eliminate temperature gradients.
The foregoing description illustrates how the sample block temperature may be controlled to be uniform and to be quickly changeable. However, in the PCR process, it is the temperature of the sample reaction mixture and not the block S, temperature that is to be programmed. In the preferred embodiment according to the teachings of the invention, the user specifies a sequence of target temperatures for the sample liquid itself and specifies the incubation times for *s 15 the sample liuid at each of these tar et temperatures for :0 each stage in the PCR process. The CPU 20 then manages the sample blck temperature so as to get the sample reaction mixtures to the specified target incuk-tion temperatures and to hold the sample mixtures at these target temperatures for the specified incubation times. The user interface code run by the CPU 20 displays, at all stages of this process, the current calculated sample liquid temperature on the display of terminal 16.
2 The difficulty with displaying an actual measured 25 sample temperature is that to measure the actual temperature of the reaction mixture requires insertion of a temperature S, measuring probe therein. The thermal mass of the probe can Ssignificantly alter the temperature of any well in which it is placed since the sample reaction mixture in any particular well is often only 100 microliters in volume.
Thus, the mere insertion of a temperature probe into a reaction mixture can cause a temperature gradient to exist between that reaction mixture and neighboring mixtures.
Since the extra thermal mass of the temperature sensor would cause the reaction mixture in which it is immersed to lag behind in temperature from the temperatures of the reaction 50 mixtures in other wells that have less thermal mass, errors can result in the amplification simply by attempting to measure the temperature.
Accordingly, the instrument described herein calculates the sample temperature from known factors such as the -block temperature history and the thermal time constant of the system and displays this sample temperature on the display.
It has been found experimentally for the system described herein that if the sample tubes are pressed down into the 10 sample wells with at least a minimum threshold force F, then for the size and shape of the sample tubes used in the preferred embodiment and the sample volumes of approximately 100 microliters, thermally driven convection occurs within S. the sample reaction mixture and the system acts thermally 15 like a single time constant, linear system. Experiments have shown that each sample tube must be pushed down with approximately 50 grams of force for good well-wall-to-liquid thermal conductivity from well to well. The heated platen design described below is designed to push down on each 20 sample tube with about 100 grams of force. This minimum force, symbolized by force vector F in Figure 15, is necessary to insure that regardless of slight differences in external dimensions as between various sample tubes and various sample wells in the sample block, they all will be pushed down with sufficient force to guarantee the snucgand flush fit for each tube to guarantee uniform thermal conductivity. Any design which has some sample tubes with loose fits in their corresponding sample wells and some tubes with tight fits will not be able to achieve tight temperature control for all tubes because of non-uniform thermal conductivity. An insufficient level of force F results in a temperature response of the sample liquid to a step change in block temperature as shown at 286 in Figure 14. An adequate level of force F results in the temperature response shown at 282.
The result achieved by the apparatus constructed 51 according to the teachings of the invention is that the temperature of each saple mixture behaveas as if the sample is being wall mixed physically during transitions to nrew temperatures. In fact, because of the Convection currents caused in each sample mixture, the sample reaction mixture in each sample tube f being well aixed.
The surprising result is that the thermal behavior of the entire system is like an electrical RC circuit with a single time constant of 9 seconds which is about 1.44 times 10 the half-life of the decay of the differanca betwoen the block temperature and the sample ta.mpertura. A GenaAmpb sampla tub* filled with 50 milliletars of sample has a time constant of about 23 seconds. In other words, during an Upward change in temperature of the sample block, the temperature of the reaction mixture acts like the rise in voltage on the capacitor C in a series RC electrical circuit like that shown in Figure 16D in response to a step change *1H in the voltage output of the voltage source V.
To illustrate these concepts, refer to Figure 14 which S 20 shows different temperature responses of the sample liquid to a stop change in block temperature and to Figure 15 which shows a cross section through a sample wall/sample tube combination. It has bean found experiientally that when the volume of sample liquid 276 is approximately 100 micro-iters 25 and the dimensions of the tube are such that the meaniscus 278 is located below the top surface 280 of the sample block 12, and the force F pushing the asample tube into the sample well is at least 30 grams, the thermal tie constant T (tau) of the system shown in Figure 15 is approximately nine seconds for a sample tube vail thickness in the conical section of 0.009 inches (dimension It has also been found experimentally that for thaese conditions, the thermal time constant T varies by about 1 second for every 0.001 inch change in wall thickness for the sample tube frustum (cone). The thin-walled sample tubes described herein have been found to have thermal time constants of from about 5 to about 14 seconds when containing from 20 to 100 microliters of sample. Thicker tube walls result in longer time constants and more lag between a change in sample block temperature 52 and the resulting change in sample liquid temperature.
Mathematically, the expression for the thermal response of the sample liquid temperature to a change in temperature of the sample block is: TSiTe AT(l-et') where Tpe the temperature of the sample liquid AT the temperature difference between the temperature of the sample block 12 and the temperature of the sample liquid t elapsed time thermal time constant of the system, or the heat capacity of sample divided by the 15 thermal conductance from sample well wall to the sample liquid In Figure 14, the curve 282 represents this exponential temperature response to a theoretical step change in sample block temperature when the force F pushing down on the 20 sample tube is sufficiently high. The step change in temperature of the sample block is shown as function 284, with rapid rise in temperature starting at time T 1 Note how the temperature of the sample liquid exponentially increases in response to the step change and asymptotically approaches the final sample block temperature. As mentioned briefly above, the curve 286 represents the thermal response when the downward seating force F in Figure 15 is insufficient to cause a snug, flush fit between the cone of the sample tube and the wall 290 of the sample well. Generally, the thermal response of curve 286 will result if the force F is less than 30 grams. Note that although Figure 15 shows a small layer of air between the cone of the sample tube and the sample well wall for clarity, this is exactly the opposite of the desired situation since air is a good insulator and would substantially increase the thermal time constant of the system.
53 The thermal time constant r is analogous to the RC time constant in a series RC circuit where R corresponds to the thermal resistance between the wall of the sample well and the sample liquid and C is the heat capacity of the sample liquid. Thermal resistance is equal to the inverse of thermal conductance which is expressed in units wattsseconds per degree Kelvin.
Because of the convection currents 292 shown in the sample liquid in Figure 15, everywhere in the reaction mixture the sample liquid is at very nearly the same temperature, and the flow of heat between the block and the sample is very nearly proportional to the difference in s* temperature between the sample block and the sample reaction mixture. The constant of proportionality is the thermal conductance between the wall of the sample well in the sample block 12 and the reaction mixture. For different sample volumes or different tubes, different wall thicknesses or materials, the thermal time constant will be different. In such a case, the user can as part of his 20 specification of the PCR protocol enter the sample volume or tube type and the machine will automatically look up the correct thermal time constant for use in calculating the sample temperature. In some embodiments, the user may enter the actual time constant, and the machine will use it for sample temperature temperature calculation.
To keep the thermal time constant as small as possible, the conical walls of the sample tubes should be as thin as possible. In the preferred embodiment, these conical walls are 0.009 inches thick whereas the walls of the cylindrical portion of the sample tube are 0.030 inches thick. The conical shape of the sample tube provides a relatively large surface area of contact with the metal of the sample well wall in relation to the volume of the sample mixture.
Molding of the sample tubes is done using a "cold runner" system and a four cavity mold such that four sample tubes are molded at each injection. The molten plastic is 54 injected at the tip of the sample tube cone so that any remnant of plastic will project into the cavity 291 between the tip of the sample tube and the tip of the sample well.
This prevents any remnant from interfering with the flush fit between the tube and the well. A maximum limit of 0.030 inches is placed on the size of any remnant plastic.
In various embodiments, 3 different grades of polypropylene each with different advantages can be used.
The preferred polypropylene is PD701 from Himont because it 10 is autoclavable. However this plastic is difficult to mold because it has a low melt index. This plastic has a melt index of 35 and a molecular density of 9. PD701 tends to leave flash and creates somewhat spotty quality parts but would work better if it was injected into the thick walled 15 part of the mold instead of at the tip of the conical section as is currently done. Generally, it is desirable to have a high melt index for ease of molding but also a high molecular density to maintain good strength and to prevent crazing or cracks under the thermal stress of the 20 autoclaving process at 2600F. Another plastic, ppW 1780 from American Hoescht has a melt index of 75 and a molecular density of 9 and is autoclavable. Another plastic which may be used in some embodiments is Himont 444. This plastic is not autoclavable and needs to be sterilized in another 25 manner.
In alternative embodiments, the tubes may be molded using a "hot runner" or "hot nozzle" system where the temperature of the molten plastic is controlled right up to the gate of the mold. Also, in some embodiments, multiple gates may be used. However, neither of these techniques has been experimentally proven at the time of filing to be better than the currently used "cold runner" system.
The fact that the system acts thermally like a single time constant RC circuit is an important result, because it means that if the thermal conductance from the sample block to the sample reaction mixture is known and uniform, the 54A thermal response of the sample mixtures will be known and uniform. Since the heat capacity of the sample reaction mixture is known and constant, the temperature of the sample reaction mixture can be computed accurately using only the measured history of the block temperature over time. This eliminates the need to measure the sample temperature thereby eliminating the errors and mechanical difficulty of putting a probe with nonnegligible thermal mass into a sample well to measure the sample temperature directly thereby changing the thermal mass of the sample in the probed well.
o'o I The algorithm which makes this calculation models the thermal behavior of the system after a single time constant series R-C electrical circuit. This model uses the ratio of 15 the heat capacity of the liquid sample divided by the thermal conductance from the sa-ple block to the sample reaction mixture. The heat capacity of the sample reaction mixture is equal to the specific heat of the liquid times the mass of the liquid. The thermal resistance is equal to S. 20 one over the thermal conductance from the sample block to the liquid'reaction mixture through the sample tube walls.
When this ratio of heat capacity divided by thermal conductance is expressed in consistent units, it has the dimension of time. For a fixed sample volume and a fixed 0oo0 25 sample composition both of which are the same in every sample well and a fixed thermal conductance, the rati5 is also a constant for every sample well, and is called the thermal time constant of the system. It is the time required for the sample temperature to come within 36.8% of the block temperature after a sudden step change in the block temperature.
There is a mathematical theorem used in the analysis of electronic circuits that holds that it is possible to calculate the output response of a filter or other linear system if one knows the impulse response of the system.
This impulse response is also known as the transfer 54B function. In the case of a series RC circuit, the impulse response is an exponential function as shown in Figure 16A.
The impulse stimulus resulting in the response of Figure 16A is as shown in Figure 16B. The mathematical theorem referred to above holds that the output response of such a linear system can be determined by calculating- the convolution of the input signal and a weighting function where the weighting function is the impulse response of the system reversed in time. The convolution is otherwise known as a running weighted average although a convolution is a concept in calculus with infinitely small step sizes whereas a running weighted average has discreet step sizes, i.e., multiple samples. The impulse response of the series RC circuit shown in Figure 16D as such that when the voltage of 15 the voltage generator V suddenly rises and falls with a S. spike of voltage as shown in Figure 16B, the voltage on the capacitor C suddenly rises to a peak at 294 in Figure 16A which is equal to the peak voltage of the impulse shown in Figure 16B and then exponentially decays back to the steady 20 state voltage V 1 The resulting weighting function is the impulse response of Figure 16A turned around in time as shown in Figure 16C at 385.
0 Superimposed upon Figure 16C is a hypothetical curve 387 illustrating a typical temperature history for the 25 temperature of the sample block 12 for an approximate step change in temperature. Also shown superimposed upon F4-gure 16C are the times of five temperature sample periods labelled T, through T 5 According to the teachings of the invention, the sample temperature is calculated by multiplying the temperature at each one of these times T, through T, by the value of the weighting function at that particular time and then summing all these products and dividing by 5. The fact that the thermal system acts like a single time constant linear circuit is a surprising result based upon the complexities of thermal heat transfer considerations for this complicated thermal system.
55 In one embodiment, the calculation of the sample temperature is adjusted by a short delay to account for transport lag caused by different thermal path lengths to the block temperature sensor and the sample liquid. The calculated sample temperature is displayed for the user's information on the terminal 16 shown in Figure 1.
Figure 17 shows the temperature response results for six different wells spread throughout the 96 well sample block for a step change in sample block temperature from a ;10 relatively lower temperature in the hybridization/extension temperature range to the relatively higher temperature of approximately 94OC used for denaturation. The graph of Figure 17 shows good agreement between the predicted exponential rise in sample temperature if the system were 15 perfectly analogous to the series RC circuit shown in Figure 16D, and also shows excellent uniformity of temperature response in that the temperatures of the six sample wells used for this study asymptotically settle in at temperatures very close to each other and in a denaturation temperature "tolerance" band which is approximately O.5C wide.
In one embodiment, the ten most recent block temperature samples are used for the running weighted average, but in other embodiments a different number of tempersature history samples may be used. The good 25 agreement with theoretically predicted results stems from the fact that the thermal convection currents make- the sample liquids well mixed thereby causing the system to act in a linear fashion.
The uniformity between sample temperatures in various sample wells spread throughout the 96 well array results from dynamic and static local balance and local symmetry in the sample block structure as well as all the other thermal design factors detailed herein. Note however that during rapid temperature changes all the sample wells will have temperatures within 0.5 0 C of each other only if the user has carefully loaded each sample well with the same mass of 56 sample liquid. Inequality of mass in different wells does not cause unequal temperatures in steady state, unchanging conditions, only during rapid changes. The mass of the sample liquid in each well is the dominant factor in determining the heat capacity of each sample and, therefore, is the dominant factor in the thermal time constant for that particular sample well.
Note that the ability to cause the sample liquid in all the sample wells to cycle up and down in temperature in S. 10 unison and to stabilize at target temperatures very near each other, in tolerance bands that are only wide, also depends upon the force F in Figure 15. -This force must exceed a minimum threshold force before the thermal time constants of all sample wells loaded with 15 similar masses of sample liquid will have the same time constant. This minimum threshold force has been experimentally determined to be 30 grams for the sample tube and sample well configuration described herein. For higher levels of accuracy, the minimum threshold force F in Figure 20 15 should be established at at least 50 grams and preferably 100 grams for an additional margin of safety as noted above.
The importance of thermal uniformity in sample well g" temperature can be appreciated by reference to Figure 18.
This figure shows the relationship between the amount of DNA generated in a PCR cycle and the actual sample temperature during the denaturation interval for one instance of amplification of a certain segment of DNA. The slope of function 298 between temperatures 93 and 95 degrees centigrade is approximately 8% per degree centigrade for this particular segment of DNA and primers. Figure 18 shows the general shape of the curve which relates the amount of DNA generated by amplification, but the details of the shape of the curve vary with every different case of primers and DNA target. Temperatures for denaturation above 97 degrees centigrade are generally too hot and result in decreasing amplification for increasing denaturation temperature.
57 Temperatures between 95 and 97 degrees centigrade are generally just right.
Figure 18 illustrates that any sample well containing this particular DNA target and primer combination which stabilizes at a denaturation temperature of approximately 93 0 C is likely to have 8% less DNA generated over the course of a typical PCR protocol than wells denatured at 94 0
C.
Likewise, sample liquids of this mixture that stabilize at denaturation temperatures of 95 0 C are likely to have 8% more 10 DNA generated therein than is generated in sample wells which stabilize at denaturation temperatures of 940C.
S Because all curves of this nature have the same general shape, it is important to have uniformity in sample temperature.
15 The sample temperatures calculated as described above O* are used by the control algorithm for controlling the heaters and flowithrough the ramp cooling channels and to determine how long the samples have been held at various target temperatures. The control algorithm uses these times 20 for comparison with the desired times for each incubation period as entered by the user. When the times match, the control algorithm takes the appropriate steps to heat or cool the sample block toward the target temperature defined by the user for the next incubation.
25 When the calculated sample temperature is within one degree centigrade of the setpoint, the incubation temperature programmed by the user, the control program causes a timer to start. This timer may be preset to count down from a number set so as to time out the interval specified by the user for the incubation being performed.
The timer starts to count down from the preset count when the calculated sample temperature is within one degree centigrade. When the timer reaches a zero count, a signal is activated which causes the CPU to take actions to implement the next segment of the PCR protocol. Any way to time the specified interval will suffice for purposes of 58 practicing the invention.
Typically, the tolerance band around any particular target temperature is plus or minus 0.50C. Once the target temperature is reached, the computer holds the sample block at the target temperature using the bias cooling channels and the film heater such that all the samples remain close to the target temperature for the specified interval.
For the thermal system described herein to work well, the thermal conductance from the sample block to each sample 10 must be known. and uniform to within a very close tolerance.
Otherwise, not all samples will be held within the specified tolerance band of the target temperature when the timer starts and, not all the samples will experience the same incubation intervals at the target temperature.
S.g 15 Also, for this thermal system to work well, all sample tubes must be isolated from variables in the ambient environment. That is, it is undesirable for some sample tubes to be cooled by drafts while other sample tubes in different physical positions do not experience the same 20 cooling effects. For good uniformity it is highly desirable that the temperatures of all the samples be determined by the temperature of the sample block and by nothing else.
Isolation of the tubes from the ambient, and application of the minimum threshold force F pushing down on 25 the sample tubes is achieved by a heated cover over the sample tubes and sample block.
Even though the sample liquid is in a sample tube pressed tightly into a temperature-controlled metal block, tightly capped, with a meniscus well below the surface of the temperature-controlled metal block, the samples still lose their heat upward by convection. Significantly, when the sample is very hot (the denaturation temperature is typically near the boiling point of the sample liquid), the sample liquid can lose a very significant amount of heat by refluxing of water vapor. In this process, water evaporates from the surface of the hot sample liquid and condenses on 59 the inner walls of the cap and the cooler upper parts of the sample tube above the top surface of the sample block. If there is a relatively large volume of sample, condensation continues, and condensate builds up and runs back down the walls of the sample tube into the reaction mixture. -This "refluxing" process carries about 2300 joules of heat per gram of water refluxed. This process can cause a drop of several degrees in the surface temperature of a 100 microliter reaction mixture thereby causing a large 10 reduction of efficiency of the reaction.
If the reaction mixture is small, say 20 microliters, and the sample tube has a relatively large surface area above the top surface of the sample block, a significant fraction of the water in the reaction mixture may evaporate.
15 This water may then condense inside the upper part of the sample tube and remain there by surface tension during the remainder of the high temperature part of the cycle. This can so concentrate the remaining reaction mixture that the reaction is impaired or fails completely.
20 In the prior art PCR thermal cyclers, this refluxing 4 problem was dealt with by overlaying the reaction mixture with a layer of oil or melted wax. This immiscible layer of oil or wax floated on the aqueous reaction mixture and prevented rapid evaporation. However, labor was required to add the oil which raised processing costs. Further -the presence of oil interfered with later steps of processing and analysis and created a possibility of contamination of the sample. In fact, it is known that industrial grade mineral oils have in the past contaminated samples by the unknown presence of contaminating factors in the oil which were unknown to the users.
The need for an oil overlay is eliminated, and the problems of heat loss and concentration of the reaction mixture by evaporation and unpredictable thermal effects caused by refluxing are avoided according to the teachings of the invention by enclosing the volume above the sample 60 block into which the upper parts of the sample tubes project and by heating this volume from above by a heated cover sometimes hereafter also called the platen.
Referring to Figure 19, there is shown a cross sectional view of the structure which is used to enclose the sample tubes and apply downward force thereto so as to supply the minimum threshold force F in Figure 15. A heated platen 14 is coupled to a lead screw 312 so as to move up and down along the axis symbolized by arrow 314 with 10 rotation of the lead screw 312. The lead screw is threaded through an opening in a sliding cover 316 and is turned by a knob 318. The platen 314 is heated to a temperature above the boiling point of water by resistance heaters (not shown) 1 controlled by computer 15 The sliding cover 316 slides back and forth along the Y axis on rails 320 and 322. The cover 316 includes vertical sides 317 and 319 and also includes vertical sides parallel to the X-Z plane (not shown) which enclose the sample block 12 and sample tubes. This structure •20 substantially prevent drafts from acting on the sample tubes of which tubes 324 and 326 are typical.
Figure 20 is a perspective view of the sliding cover 316 and sample block 12 with the sliding cover in retracted position to allow access to the sample block. The sliding 25 cover 316 resembles the lid of a rectangular box -ith vertical wall 328 having a portion 330 removed to allow the 06 o sliding cover 316 to slide over the sample block 12. The sliding cover is moved along the Y axis in Figure 20 until the cover is centered over the sample block 12. The user then turns the knob 318 in a direction to lower the heated platen 14 until a mark 332 on the knob 318 lines up with a mark 334 on an escutcheon plate 336. In some embodiments, the escutcheon plate 336 may be permanently affixed to the top surface of the sliding cover 316. In other embodiments, the escutcheon 336 may be rotatable such that the index mark 334 may be placed in different positions when different size 61 sample tubes are used. In other words, if taller sample tubes are used, the heated platen 14 need not be lowered as much to apply the minimum threshold force F in Figure In use, the user screws the screw 318 to lower the platen 14 until the index marks line up. The user then knowsz that the minimum threshold force F will have been applied to each sample tube.
Referring jointly to Figures 15 and 19, prior to lowering the heated platen 14 in Figure 19, the plastic cap 338 for each sample tube sticks up about 0.5 millimeters above the level of the top of the walls of a plastic tray Se.* 340 (Figure 19) which holds all the sample tubes in a loose 8x12 array on 9 millimeter centers. The array of sample wells can hold up to 96 MicroAmpb PCR tubes of 100 pL 15 capacity or 48 larger GeneAmp tubes of 0.5 ml capacity.
The details of this tray will be discussed in greater detail S below. The tray 340 has a planar surface having an 8x12 array of holes for sample tubes. This planar surface is shown in Figures 15 and 19 as a horizontal line which intersects the sample tubes 324 and 326 in Figure 19. Tray 340 also has four vertical walls two of which are shown at 342 and 344 in Figure 19. The top level of these vertical walls, shown at 346 in Figure 15, establishes a rectangular box which defines a reference plane.
25 As best seen in Figure 15, the caps 338 for allthe sample tubes project above this reference plane 346 by-some small amount which is designed to allow the caps 338 to be softened and deformed by the heated platen 14 and "squashed" down to the level of the reference plane 346. In the preferred embodiment, the heated platen 14 is kept at a temperature of 1050C by the CPU 20 in Figure 1 and the bus 22 coupled to resistance heaters (not shown) in the platen 14. In the preferred embodiment, the knob 318 in Figure 19 and the lead screw 312 are turned until the heated platen 14 descends to and makes contact with the tops of the caps 338.
In the preferred embodiment, the caps 338 for the sample 62 tubes are made of polypropylene These caps soften shortly after they come into contact with the heated platen 14. As the caps soften, they deform, but they do not lose all of their elasticity. After contacting the caps, the heated platen is lowered further until it rests upon the reference plane 346. This further lowering deforms the caps 338 and causes a minimum threshold force F of at least 50 grams to push down on each sample tube to keep each tube well seated firmly in its sample well. The amount by which the caps 338 project above the reference plane 346, and the amount of deformation and residual elasticity when the heated platen 14 rests upon the reference plane 346 is designed such-that a minimum threshold force F of at least 50 grams and 0 preferably 1oo grams will have been achieved for all sample 15 tubes then present after the heated platen 14 has descended to the level of the reference plane 346.
The heated platen 14 and the four vertical walls and planar surface of the tray 340 form a heated, sealed compartment when the platen 14 is in contact with the top edge 346 of the tray. The plastic of the tray 340 has a relatively poor thermal conductivity property. It has been found experimentally that contacting the heated platen 14 with the caps 338 and the isolation of the portion of the sample tubes 288 which project above the top level 280 of 25 the sample block 12 by a wall of material which__has relatively poor thermal conductivity has a beneficial result. With this structure, the entire upper part of the tube and cap are brought to a temperature which is high enough that little or no condensation forms on the inside surfaces of the tube and cap since the heated platen is kept at a temperature above the boiling point of water. This is true even when the sample liquid 276 in Figure 15 is heated to a temperature near its boiling point. This eliminates the need for a layer of immiscible material such as oil or wax floating on top of the sample mixture 276 thereby reducing the amount of labor involved in a PCR reaction and 63 eliminating one source of possible contamination of the sample.
It has been found experimentally that in spite of the very high temperature of the heated cover and its close proximity to the sample block 12, there is little affect on the ability of the sample block 12 to cycle accurately and rapidly between high and low temperatures.
The heated platen 14 prevents cooling of the samples by the refluxing process noted earlier because it keeps the temperature of the caps above the condensation point of water thereby keeping the insides of the caps dry. This also prevents the formation of aerosols when the caps are OO.o removed from the tubes.
In alternative embodiments, any means by which the 15 minimum acceptable downward force F in Figure 15 can be applied to each individual sample tube regardless of the number of sample tubes present and which will prevent condensation and refluxing and convection cooling will suffice for purposes of practicing the invention. The application of this downward force F and the use of heat to prevent refluxing and undesired sample liquid concentration need not be both implemented by the same system as is done in the preferred embodiment.
The sample tubes may vary by a few thousandths of an 25 inch in their overall height. Further, the caps for-the sample tubes may also vary in height by a few thousandths of an inch. Also, each conical sample well in the sample block 12 may not be drilled to exactly the same depth, and each conical sample well in the sample block may be drilled to a slightly different diameter and angle. Thus, when a population of capped tubes is placed in the sample block so as to be seated in the corresponding sample well, the tops of the caps will not all necessarily be at the same height.
The worst case discrepancy for this height could be as much as 0.5 millimeters from the highest to the lowest tubes.
If a perfectly flat unheated platen 14 mounted so that 64 it is free to find its own position were to be pressed down on such an array of caps, it would f irst touch the three tallest tubes. As further pressure was applied and the tallest tubes were compressed somewhat, the platen would begin to touch some caps of lower tubes. There Is a distinct possibility that unless the tube and cap assemblies were compliant, the tallest tubes wou 'ld be damaged before the shortest tubes were contacted at all. Alternatively, the force necessary to compress all the tall tubes sufficiently so as to contact the shortest tube could be too- S large for the device to apply. In either case, one or more short tubes might not be pressed down at all or might be Ses, pressed down with an insufficient amount of force to guarantee that the thermal time constant for that tube was *5..15 equal to the thermal time constants for all the other tubes.
This would result in the failure to achieve the same PCR cycle for all tubes in the sample block since some tubes with different thermal time constants woulc not be in step with the other tubes. Heating the platen and softening the caps eliminates these risks by eliminatin g the manufacturing tolerance errors which lead to differing tube heights as a factor.
:In an alternative embodiment, the entire heated platen *14 is covered with a compliant rubber layer. A compliant @0 0 25 rubber layer on the heated platen would solve the hei-ght tolerance problem, but would also act as a thermal insulation layer which would delay the flow of heat from the heated platen to the tube caps. Further, with long use at high temperatures, most rubber materials deteriorate or become hard. It is therefore desirable that the heated platen surface be a metal and a good conductor of heat.
In another alternative embodiment, 96 individual springs could be mounted on the platen so that each spring individually presses down on a single sample tube. This is a complex and costly solution, however, and it requires that the platen be aligned over the tube array with a mechanical 65 precision which would be difficult or bothersome to achieve.
The necessary individual compliance for each sample tube in the preferred embodiment is supplied by the use of plastic caps which collapse in a predictable way under the force from the platen but which, even when collapsed,-still exert a downward force F on the sample tubes which is adequate to keep each sample tube seated firmly in its well.
In the sample tube cap 338 shown in Figure 15, the surface 350 should be free of nicks, flash and cuts so that it can provide a hermetic seal with the inner walls 352 of the sample tube 288. In the preferred embodiment, the material for the cap is polypropylene. A suitable material might be Valtec HH-444 or PD701 polypropylene manufactured by Himont as described above or PPW 1780 by American 15 Hoescht. In the preferred embodiment, the wall thickness for the domed portion of the cap is 0.130 .000 0.005 inches. The thickness of the shoulder portion 356 is 0.025 inches and the width of the domed shaped portion of the cap is 0.203 inches in the preferred embodiment.
Any material and configuration for the caps which will cause the minimum threshold force F in Figure 15 to be applied to all the sample tubes and which will allow the cap and upper portions of the sample tubes to be heated to a temperature high enough to prevent condensation and 25 refluxing will suffice for purposes of practicing- the invention. The dome shaped cap 338 has a thin wall to aid in deformation of the cap. Because the heated platen is kept at a high temperature, the wall thickness of the domed shaped cap can be thick enough to be easily manufactured by injection molding since the necessary compliance to account for differences in tube height is not necessary at room temperature.
The platen can be kept at a temperature anywhere from 94C to 110 0 C according to the teachings of the invention although the range from 100'C to 1100C is preferred to prevent refluxing since the boiling point of water is 100°C.
66 In this temperature range, it has been experimentally found that the caps soften just enough to collapse easily by as much as 1 millimeter. Studies have shown that the elastic properties of the polypropylene used are such that even at these temperatures, the collapse is not entirely inelastic.
That is, even though the heated platen causes permanent deformation of the caps, the material of the caps still retain a significant enough fraction of their room temperature elastic modulus that the minimum threshold force F is applied to each sample tube. Further, the heated platen levels all the caps that it contacts without excessive force regardless of how many tubes are present in the sample block because of the softening of the cap.
Because the cap temperature is above the boiling point 15 of water during the entire PCR cycle, the inside surfaces of Se.: each cap remain completely dry. Thus, at the end of a PCR process, if the samples are cooled to room temperature before being removed from the sample block, if the caps on each sample tube are opened, there is no possibility of 20 creating an aerosol spray of the sample tube contents which could result in cross contamination. This is because there is no liquid at the cap to tube seal when the seal is broken.
a This is extremely advantageous, because tiny particles 25 of aerosol containing amplified product DNA can contaminate a laboratory and get into sample tubes containing samples from other sources, other patients, thereby possibly causing false positive or negative diagnostic results which can be very troublesome. Users of the PCR amplification process are extremely concerned that no aerosols that can contaminate other samples be created.
A system of disposable plastic items is used to convert the individual sample tubes to an 8x12 array which is compatible with microtiter plate format lab equipment but which maintains sufficient individual freedom of movement to compensate for differences in the various rates of thermal 67 expansion of the system components. The relationship of the thermally compliant cap to the rest of this system is best seen in Figure 21A which is a cross sectional view of the sample block, and two sample tubes with caps in place with the sample tubes being held in place by the combination of one embodiment of a plastic 96 well microtiter tray and a retainer. Figure 21B is an alternative, preferred embodiment showing the structure and interaction of most of the various plastic disposable items of the system. The rectangular plastic 96 well microtiter plate tray 342 rests on the surface of the sample block 12. The top edge 346 of the frame 342 has a height which is approximately millimeters shorter than the height of the caps of which cap 364 is exemplary. All of the capped tubes will project 9o 15 higher than the edge 346 of the frame 342. The frame 342 is configured such that a downward extending ridge 366 extends into the guardband groove 78 through its entire length. The frame 342 does however have a gap (not shown) which corresponds to the gap in the groove 78 for the temperature A 20 sensor shown in Figure 2 in plan view and in Figure 7 in cross-sectional view.
The reference plane 346 mentioned above is established by the top of the frame 342. How this reference plane interacts with the heated platen is as follows. Prior to .ooo 25 screwing down the knob 318 in Figure 20 to line up thejindex marks 332 and 334 to start an amplification run, a calibration process will have been performed to locate the position of the index mark on the escutcheon platen 336 in Figure 20. This calibration is started by placing the frame 342 in Figure 21 in position on the sample block. The frame 342 will be empty however or any sample tubes therein will not have any caps in place. Then, the knob 318 is screwed down until the heated platen 14 is firmly in contact with the top edge 346 of the frame 342 around its entire parameter. When the knob 318 has been screwed down sufficiently to allow the heated platen to reast on the 68 reference plane 346 and to press the frame 342 firmly against the top surface 280 of the sample block, the rotatable escutcheon 336 of the preferred embodiment will be rotated until the index mark 334 on the escutcheon lines up with the index mark 332 on the knob 318. Then, the knob 318 is rotated counterclockwise to raise the platen 14 and the cover 316 in Figure 19 is slid in the negative Y direction to uncover the frame 342 and the sample block 12. Sample tubes with caps loaded with a sample mixture may then be placed in position in the frame 342. The heated cover 316 is then placed back over the sample block, and the knob 318 is turned clockwise to lower the heated platen 14 until the index mark 332 on the knob lines up with the index mark 334 as previously positioned. This guarantees that all tubes 15 have been firmly seated with the minimum force F applied.
*00 The use of the index marks gives the user a simple, verifiable task to perform.
If there are only a few sample tubes in place, it will take only a small amount of torque to line up the index 20 marks 332 and 334. If there are many tubes, however, it 4 will take more torque on the knob 318 to line up the index marks. This is because each tube is resisting the downward movement of the heated platen 14 as the caps deform.
U* However, the user is assured that when the index marks 332 25 and 334 are aligned, the heated platen will once again be tightly placed against the top edge 346 of the frame 342 and all tubes will have the minimum threshold force F applied thereto. This virtually guarantees that the thermal time constant for all the tubes will be substantially the same.
In alternative embodiments, the index marks 332 and 334 may be dispensed with, and the knob 318 may simply be turned clockwise until it will not turn any more. This condition will occur when the heated platen 314 has reached the top edge or reference plane 346 and the plastic frame 342 has stopped further downward movement of the heated platen 14.
Obviously in this alternative embodiment, and preferably in 69 the index mark embodiment described above, the plastic of the frame 342 will have a melting temperature which is sufficiently high to prevent deformation of the plastic of the frame 342 when it is in contact with the heated platen 14. In the preferred embodiment, the plastic of the frame 342 is celanese nylon 1503 with a wall thickness of 0.05 inches.
An advantage of the above described system is that sample tubes of different heights may be used simply by using frames 342 having different heights. The frame 342 should have a height which is approximately 0.5 millimeters shorter than the plane of the tips of the capped tubes when both are seated in the sample block. In the preferred embodiment, two different tube heights are used. The range 15 of motion of the lead screw 312 which drives the heated platen 14 in Figure 19 must be sufficient for all the different sizes of sample tubes to be used. Of course, during any particular PCR processing cycle, all tubes must be the same height.
20 The system described above provides uniform temperatures in the sample block, uniform thermal conductance from block to sample, and isolation of the sample tubes from the vagaries of the ambient environment.
Any number of sample tubes up to 96 may be arrayed in the 25 microtiter plate format. The system allows accurate temperature control for a very large number of samples and a visual indication of the sample temperatures for all samples without actually measuring the temperature of any sample.
As the container for PCR reactions, it has been common in the prior art to use polypropylene tubes which were originally designed for microcentrifuges. This prior art tube had a cylindrical cross-section closed at the top by a snap-on cap which makes a gas-tight seal. This prior art tube had a bottom section which comprised the frustrum of a cone with an included angle of approximately 17 degrees.
70 0 0000
S
0 5000 0 S. a. 0 When such a conical sample tube is pressed down into a sample well of a sample block with a conical cavity with the same included angle, and when the sample mixture in the tube lies entirely within the conical volume and below the top surface of the sample block, the thermal conductance between the block and the liquid can be made adequately predictable for good uniformity of sample temperature throughout the array. To achieve adequate control of the thermal conductance between the sample block and the sample mixture, the included angles of the conical tube and the sample well must match closely, and the conical surfaces of the tube and well must be smooth and held together in flush relation.
Further, the minimum threshold force F must be applied to each sample tube to press each tube tightly into the sample 15 well so that it does not rise up or loosen in the well for any reason during thermal cycling, such as steam formation from trapped liquid in space 291 in Figure 15. Finally, each tube must be loaded with the same amount of sample liquid. If the above listed conditions are met, the thermal conductance between the sample block and the sample liquid in each tube will be predominantly determined by the conductance of the conical plastic wall 368 in Figure 15 and a boundary layer, (not shown) of the sample liquid at the inside surface 370 of the conical sample tube wall.
The thermal conductance of the plastic tube walls is determined by their thickness, which can be closely controlled by the injection molding method of manufacture of the tubes. The sample liquid in all the sample tubes has virtually identical thermal properties.
It has been found by experiment and by calculation that a molded, one-piece, 96-well microtiter plate is only marginally feasible for PCR because the differences in the thermal expansion coefficients between aluminum and plastic lead to dimensional changes which can destroy the uniformity of thermal conductance to the sample liquid across the array. That is, since each well in such a one-piece plate 71 is connected to each other well through the surface of the plate, the distances between the wells are determined at the time of initial manufacture of the plate but change with changing temperature since the plastic of the plate has a significant coefficient of thermal expansion. Also, distances between the sample wells in the metal sample block 12 are dependent upon the temperature of the sample block since aluminum also has a significant coefficient of thermal expansion which is different than that of plastic. To have good thermal conductance, each sample well in a one-piece 96-well microtiter plate would have to fit almost perfectly in the corresponding well in the sample block at all temperatures. Since the temperature of the sample block changes over a very wide range of temperatures, the 15 distances between the sample wells in the sample block vary cyclically during the PCR cycle. Because the coefficients of thermal expansion for plastic and aluminum are substantially different, the distances of the well o* separation in the sample block would vary differently over changing temperatures than would the distances between the sample wells of a plastic, one-piece, 96-well microtiter plate.
Thus, as an important criteria for a perfect fit between a sample tube and the corresponding sample well over the PCR temperature range, it is necessary that each sample tube in the 96-well array be individually free to move laterally and each tube must be individually free to be pressed down vertically by whatever amount is necessary to make flush contact with the walls of the sample well.
0 30 The sample tubes used in the invention are different from the prior art microcentrifuge tubes in that the wall thickness of the conical frustrum position of the sample tube is much thinner to allow faster heat transfer to and from the sample liquid. The upper part of these tubes has a thicker wall thickness than the conical part. In Figure the wall thickness in the cylindrical part 288 in Figure 72 is generally 0.030 inches while the wall thickness for the conical wall 368 is 0.009 inches. Because thin parts cool faster than thick parts in the injection molding process, it is important to get the mold full before the thin parts cool off.
The material of the sample tubes must be compatible chemically with the PCR reaction. Glass is not a PCR compatible material, because DNA sticks to glass and will not come of f which would interfere with PCR amplification.
Preferably an autoclavable polypropylene is used. Three types of suitable polypropylene were identified earlier herein. Some plastics are not compatible with the PCR process because of outgassing of materials from the plastic or because DNA sticks to the plastic walls. Polypropylene is the best known class of plastics at this time.
Conventional injection molding techniques and mold manufacture techniques for the injection mold will suffice 0 0 for purposes of practicing the invention.
*006 0* a* The use of cone shaped sample tubes translates substantially all manufacturing tolerance errors to height errors, a variance from tube to tube in the height of the tip of the cap to the top of the *sample block when the sample tube is seated in the sample well. For example, an angle error for the angle of the sample tube walls is converted to a height error when the tube is placed ilAthe *sample block because of the mismatch between the tube-wall angle and the sample well wall angle. Likewise, a diameter error in the dimensions of the cone would also translate into a height error since the conical part of the tube would either penetrate deeper or not as much as a properly dimensional tube.
For good uniformity of thermal conductance across the array, a good fit between the sample tubes and the sample well must exist for all 96-wells over the full temperature range of 0 to 100 0 C regardless of differences in thermal expansion rates. Also, each of the 96 sample tubes must 73 have walls with dimensions and wall thicknesses which are uniform to a very high degree. Each sample tube in which sample mixture is to be held should be fitted with a removable gas-tight cap that makes a gas-tight seal to prevent loss of water vapor from the reaction mixture-when this mixture is at or near its boiling point such that the volume of the sample mixture does not decrease. All these factors combine to make a one-piece microtiter plate with 96 individual sample wells extremely difficult to manufacture in a manner so as to achieve uniform thermal conductance for all 96 wells.
Any structure which provides the necessary individual lateral and vertical degrees of freedom for each sample tube S. will suffice for purposes of practicing the invention.
15 According to the teachings of the preferred embodiment of the invention, all the above noted requirements have been met by using a 4 piece disposable plastic system. This S. S system gives each sample tube sufficient freedom of motion in all necessary directions to compensate for differing rates of thermal expansion and yet retains up to 96 sample tubes in a 96 well microtiter plate format for user convenience and compatibility with other laboratory equipment which is sized to work with the industry standard 96-well microtiter plate. The multi-piece disposable plastic system is very tolerant of manufacturing tole rance errors and the differing thermal expansion rates over the wide temperature range encountered during PCR thermal cycling.
Figures 21A and 21B show alternative embodiments of S" 30 most of the four piece plastic system components in crosssection as assembled to hold a plurality of sample tubes in their sample wells with sufficient freedom of motion to account for differing rates of thermal expansion. Figure shows all the parts of the disposable plastic microtiter plate emulation system in an exploded view. This figure illustrates how the parts fit together to form a microtiter 74 plate with all the sample tubes loosely retained in an 8x12 microtiter plate format 96 well array. Figure 22 shows a plan view of a microtiter plate frame 342 according to the teachings of the invention which is partially shown in cross-section in Figures 21A and 21B. Figure 23 shows a bottom view plan view of the frame 342. Figure 24 is an end view of the frame 342 taken from view line 24-24' in Figure 22. Figure 25 is an end view of the frame 342 taken from view line 25-25' in Figure 22. Figure 26 is a cross section through the frame 342 at section line 26-26' in Figure 22.
Figure 27 is a cross sectional view through the frame 342 taken along section line 27-27' in Figure 22. Figure 28 is a side view of the frame 342 taken along view line 28-28' in Figure 22 with a partial cut away to show in more detail the 15 location where a retainer to be described below clips to the frame 342.
Referring jointly to Figures 21A, 21B and 22 through 28, the frame 342 is comprised of a horizontal plastic plate S372 in which there are formed 96 holes spaced on 9 millimeter centers in the standard microtiter plate format.
There are 8 rows labeled A through H and 12 columns labeled 1 through 12. Hole 374 at row D, column 7 is typical of these holes. In each hole in the frame 342 there is placed a conical sample tube such as the sample tube 376 shown in 25 Figure 15. Each sample tube is smaller in diameter than the .0 hole in which it is placed by about 0.7 millimeters, so-that there is a loose fit in the hole. This is best seen in Figures 21A and 21B by observing the distance between the inside edge 378 of a typical hole and the side wall 380 of 30 the sample tube placed therein. Reference numeral 382 in Figures 21A and 21B shows the opposite edge of the hole which is also spaced away from the outside wall of the cylindrical portion of the sample tube 376.
Each sample tube has a shoulder shown at 384 in Figures 15, 21A and 21B. This shoulder is molded around the entire circumference of the cylindrical portion 288 of each sample 75 tube. The diameter of this shoulder 384 is large enough that it will not pass through the holes in the frame 342, yet not so large as to touch the shoulders of the adjacent tubes in neighboring holes.
Once all the tubes are placed in their holes in-the frame 342, a plastic retainer 386 (best seen in Figures 21A and 21B and Figure 45) is snapped into apertures in the frame 342. The purpose of this retainer is to keep all the tubes in place such that they cannot fall out or be knocked out of the frame 342 while not interfering with their looseness of fit in the frame 342. The retainer 386 is sized and fitted to the frame 342 such that each sample tube has freedom to move vertically up and down to some extent before the shoulder 384 of the tube encounters either the 15 retainer 386 or the frame 342. Thus, the frame and retainer, when coupled, provide a microtiter plate format for up to 96 sample tubes but provide sufficient horizontal 0* and vertical freedom such that each tube is free to find its best fit at all temperatures under the influence of the minimum threshold force F in Figure A more clear view of the sample tube and shoulder may be had by reference to Figures 29 and 30. Figures 29 and are an elevation sectional view and a partial upper section of the shoulder portion, respectively, of a typical sample 25 tube. A plastic dome-shaped cap such as will be described in more detail below is inserted into the sample tube shown 0 in Figure 29 and forms a hermetic seal with the inside wall 390 of the top at the sample tube. A ridge 392 formed in the inside wall of the sample tube acts as a stop for the S. 30 dome-shaped cap to prevent further penetration. Normally, the dome-shaped caps come in strips connected by web.
Figure 31 shows three caps in elevation view connected by a web 394 and terminated in a tab 396. The tab aids the user in removing an entire row of caps by a single pull.
Normally, the web 394 rests on the top surface 398 of the sample tube and prevents further penetration of the cap into 76 the sample tube. Each cap includes a ridge 400 which forms the hermetic seal between the cap and the inside wall of the sample tube. Figure 32 shows a top view of three caps in a typical strip of 12 connected caps.
For a more detailed understanding of the retainer, refer to Figures 33 through 37. Figure 33 is a top view of the plastic retainer. Figure 34 is an elevation view of the retainer taken along view line 34-34' in Figure 33. Figure is an end elevation view of the retainer taken along view line 35-35' in Figure 33. Figure 36 is a sectional view taken along section line 36-36' in Figure 33. Figure 37 is a sectional view through the retainer taken along section line 37-37' in Figure 33.
Referring jointly to Figures 33-37, the retainer 386 is 15 comprised of a single horizontal plastic plane 402 surrounded by a vertical wall 404. The plane 402 has an 8 ooo x 12 array of 96 holes formed therein divided into 24 groups of four holes per group. These groups are set off by ridges formed in the plane 402 such as ridges 406 and 408. Each hole, of which hole 410 is typical, has a diameter D which is larger than the diameter D, in Fig. 29 and smaller than the diameter
D
2 This allows the retainer to be slipped over the sample tubes after they have been placed in the frame 9* 342 but prevents the sample tubes from falling out of the 25 frame since the shoulder 384 is too large to pass through the hole 410.
The retainer snaps into the frame 342 by means of plastic tabs 414 shown in Figures 34 and 36. These plastic S tabs are pushed through the slots 416 and 418 in the frame 30 as shown in Figure 23. There are two plastic tabs 414, one 0* 0 on each long edge of the retainer. These two plastic tabs are shown as 414A and 414B in Figure 33.
The frame 342 of Figures 22-28, with up to 96 sample tubes placed therein and with the retainer 386 snapped into place, forms a single unit such as is shown in Figures 21A and 21B which can be placed in the sample block 12 for PCR 77 processing.
After processing, all the tubes may be removed simultaneously by lifting the frame 342 out of the sample block. For convenience and storage, the frame 342 With sample tubes and retainer in place can be inserted -into another plastic component called the base. The base has the outside dimensions and footprint of a standard 9 6-well microtiter plate and is shown in Figures 38 through 44.
Figure 38 is a top plan view of the base 420, while Figure 39 is a bottom plan view of the base. Figure 40 is an elevation view of the base taken from view line 40-40' i n Figure 38. Figure 41 is an end elevation view taken..from view line 41-41' in Figure 38. Figure 42 is a sectional view taken through the base along section line 42-42' in Figure 38. Figure 43 is a sectional view through the base *see taken along section line 43-43' in Figure 38. Figure 44 is s a sectional view taken al ong section line 44-44' in Figure 38.
The base 420 includes a flat plane 422 of plastic in which an 8 x 12 array of loles with sloped edges is formed.
These holes have dimensions and spacing such that when the frame 342 is seated in the base, the bottoms of the sample tubes fit into the conical holes in the base such that the sample tubes are held in the same relationship to the frame 342 as the sample tubes are held when the frame 342 i mounted on the sample block. Hole 424 is typical of Vie- 96 holes formed in the base and is shown in Figures 38, 44 and *:*see 43. The individual sample tubes, though loosely captured between the tray and retainer, become firmly seated and :0 immobile when the frame is inserted in the base. The manner in which a-typical sample tube 424 fits in the base is shown in Figure 44.
In other words, when the frame, sample tubes and retainer are seated in the base 420 the entire assembly becomes the exact functional equivalent of an industry standard 96-well microtiter plate, and can be placed in 78 virtually any automated pipetting or sampling system for 96well industry standard microtiter plates for further processing.
After the sample tubes have been filled with the necessary reagents and DNA sample to be amplified, the sample tubes can be capped. In an alternative embodiment of the cap strip shwon in Figures 31 and 32, an entire mat of 96 caps with a compliant web connecting them in an 8 x 12 array may be used. This web, shown at 394 in Figure 31 must be sufficiently compliant so that the caps do not restrain the sample tubes from making the small motions these sample tubes must make to fit perfectly in the conical wells of the sample block at all temperatures.
The assembly of tubes, caps frames, retainer and base 15 is brought after filling the tubes to the thermal cycler.
There, the frame, capped tubes and retainer plate are removed from the base as a unit. This unit is then placed in the sample block 12 to make the assembly shown in Figure 21A or 21B with the tubes loosely held in the conical wells in the sample block. As shown in Figure 21, the frame 342 is seated on the top surface 280 of the guardband. In the preferred embodiment, the ridge 366 extends down into the groove 78 of the guardband, but this is not essential.
Next, the heated cover is slid over the samples, and 25 the heated platen is screwed down as previously described until it contacts the top edge 346 of the frame 342.
**Within seconds after the heated platen 14 in Figure 19 touches the caps, the caps begin to soften and yield under the downward pressure from the lead screw 312 in Figure 19.
30 The user then continues to turn to knob 318 until the index marks 332 and 334 in Figure 20 line up which indicates that every sample tube has been tightly pressed into the sample block with at least the minimum threshold force F and all air gaps between the heated platen 14, the sample block and the top edge 346 of the frame 342 have been tightly closed.
The sample tubes are now in a completely closed and 79 controlled environment, and precision cycling of temperature can begin.
At the end of the PCR protocol, the heated platen 14 is moved upward and away from the sample tubes, and the heated cover 316 is slid out of the way to expose the frame 342 and sample tubes. The frame, sample tubes and retainer are then removed and replaced into an empty base, and the caps can be removed. As each cap or string of caps is pulled off, the retainer keeps the tube from coming out of the tray. Ribs formed in the base (not shown in Figures 38-44) contact the retainer tabs 414A and 414B shown in Figure 33 to keep the retainer snapped in place such that the force exerted on the tubes by removing the caps does not dislodge the retainer o 386.
15 Obviously, the frame 342 may be used with fewer than 96 tubes if desired. Also, the retainer 386 can be removed if desired by unsnapping it.
A user who wishes to run only a few tubes at a time and handle these tubes individually can place an empty frame 342 without retainer on the sample block. The user may then use the base as a "test tube rack" and set up a small number of tubes therein. These tubes can then be filled manually and capped with individual caps. The user may then transfer the tubes individually into wells in the sample block, close the 25 heated cover and screw down the heated platen 14 until the marks line up. PCR cycling may then commence. When the cycling is complete, the cover 316 is removed and the sample tubes are individually placed in an available base. The retainer is not necessary in this type of usage.
30 Referring to Figures 47A and 47B (hereafter Figure 47), there is shown a block diagram for the electronics of a preferred embodiment of a control system in a class of control systems represented by CPU block 10 in Figure 1i.
The purpose of the control electronics of Figure 47 is, inter alia, to receive and store user input data defining the desired PCR protocol, read the various temperature 80 sensors, calculate the sample temperature, compare the calculated sample temperature to the desired temperature as defined by the user defined PCR protocol, monitor the power line voltage and control the film heater zones and the ramp cooling valves to carry out the desired temperature profile of the user defined PCR protocol.
A microprocessor (hereafter CPU) 450 executes the control program described below and given in Appendix C in source code form. In the preferred embodiment, the CPU 450 is an OKI CMOS 8085. The CPU drives an address bus 452 by which various ones of the other circuit elements in Figure 47 are addressed. The CPU also drives a data bus 454 by which data is transmitted to various of the other circuit 0 o elements in Figure 47.
.15 The control program of Appendix C and some system constants are stored in EPROM 456. User entered data and other system constants and characteristics measured during the install process (install program execution described: below) are stored in battery backed up RAM 458. A system clock/calendar 460 supplies the CPU 450 with date and time information for purposes of recording a history of events during PCR runs and the duration of power failures as described below in the description of the control software.
*An address decoder 462 receives and decodes addresses -25 from the address bus 452 and activates the appropriate chip S. select lines on a chip select bus 464. The user enters PCR protocol data via a keyboard 466 in response to information displayed by CPU on display 468.
The two way communication between the user and the CPU 450 30 is described in more detail below in the user interface section of the description of the control software.
A
keyboard interface circuit 470 converts user keystrokes to data which is read by the CPU via the data bus 454.
Two programmable interval timers 472 and 474 each contain counters which are loaded with counts calculated by the CPU 450 to control the intervals during which power is 81 applied to the various film heater zones.
An interrupt controller 476 sends interrupt requests to the CPU 450 every 200 milliseconds causing the CPU 450 to run the PID task described below in the description of the control software. This task reads the temperature sensors and calculates the heating or cooling power necessary to move the sample temperature from its current level to the level desired by the user for that point in time in the PCR protocol being executed.
A UART 478 services an RS232 interface circuit 480 such that data stored in the RAM 480 may be output to a printer.
The control software maintains a record of each PCR run which is performed with respect to the actual temperatures which existed at various times during the run for purposes 15 of user validation that the PCR protocol actually executed corresponded to the PCR protocol desired by the user. In addition, user entered data defining the specific times and temperatures desired during a particular PCR protocol is also stored. All this data and other data as well may be read by the CPU 450 and output to a printer coupled to the RS232 port via the UART 478. The RS232 interface also allows an external computer to take control of the address and data buses for purposes of testing.
A peripheral interface chip (hereafter PIC) 482 serves 25 as a programmable set of 4 input/output registers. At power-up, the CPU 450 selects the PIC 482 via the address decoder 462 and the chip select bus 464. The CPU then writes a data word to the PIC via data bus 454 to program the PIC 482 regarding which registers are to be output ports 30 and which are to be input ports. Subsequently, the CPU 450 uses the output registers to store data words written therein by the CPU via the data bus 454 to control the internal logic state of a programmable array logic chip (PAL) 484.
The PAL 484 is a state machine which has a plurality of input signals and a plurality of output signals. PAL's in 82 general contain an array of logic which has a number of different states. Each state is defined by the array or O vector of logic states at the inputs and each state results in a different array or vector of logic states on the outputs. The CPU 450, PIC 482, PAL 484 and several other circuits to be defined below cooperate to generate different states of the various output signals from the PAL 484.
These different states and associated output signals are what control the operation of the electronics shown in Figure 47 as will be described below.
A 12 bit analog-to-digital converter 486 converts analog voltages on lines 488 and 490 to digital signals on data bus 454. These are read by the CPU by generating an address for the A/D converter such that a chip select signal 15 on bus 464 coupled to the chip select input of the A/D converter goes active and activates the converter. The analog signals on lines 488 and 490 are the output lines of two multiplexers 492 and 494. Multiplexer 492 has four inputs ports, each having two signal lines. Each of these 20 ports is coupled to one of the four temperature sensors in -the system. The first port is coupled to the sample block temperature sensor. The second and third ports are coupled to the coolant and ambient temperature sensors, respectively and the fourth port is coupled to the heated cover S* 25 temperature sensor. A typical circuit for each one of these temperature sensors is shown in Figure 48. A 20,000 ohm resistor 496 receives at a node 497 a regulated +15 -volt regulated power supply 498 in Figure 47 via a bus connection line which is not shown. This +15 volts D.C. signal reverse biases a zener diode 500. The reverse bias current and the voltage drop across the zener diode are functions of the temperature. The voltage drop across the diode is input to the multiplexer 292 via lines 502 and 504. Each temperature sensor has a similar connection to the multiplexer 292.
Multiplexer 494 also has 4 input ports but only three are connected. The first input port is coupled to a 83 calibration voltage generator 506. This voltage generator outputs two precisely controlled voltage levels to the multiplexer inputs and is very thermally stable. That is, the reference voltage output by voltage source 506 drifts very little if at all with temperature. This voltage is read from time to time by the CPU 450 and compared to a stored constant which represents the level this reference voltage had at a known temperature as measured during execution of the install process described below. If the reference voltage has drifted from the level measured and stored during the install process, the CPU 450 knows that the other electronic circuitry used for sensing the various S temperatures and line voltages has also drifted and adjusts their outputs accordingly to maintain very accurate control 15 over the temperature measuring process.
The other input to the multiplexer 494 is coupled via line 510 to an RMS-to-DC converter circuit 512. This *0 circuit has an input 514 coupled to a step-down transformer 516 and receives an A.C. voltage at input 514 which is proportional to the then existing line voltage at A.C. power input 518. The RMS-to-DC converter 512 rectifies the A.C.
voltage and averages it to develop a D.C. voltage on line 510 which also is proportional to the A.C. input voltage on line 518.
25 Four optically coupled triac drivers 530, 532, 534 and 536 receive input control signals via control bus 538-from S PAL logic 484. Each of the triac drivers 530, 532 and 534 *e controls power to one of the three film heater zones. These heater zones are represented by blocks 254, 260/262 and *4 30 256/258 (the same reference numerals used in Figure 13).
The triac driver 536 controls power to the heated cover, represented by block 544 via a thermal cut-out switch 546.
The heater zones of the film heater are protected by a block thermal cutout switch 548. The purpose of the thermal cutout switches is to prevent meltdown of the film heater/sample block on the heated cover in case of a failure 84 leading to the triac drlvers being left on for an unsafe interval. If such an event happens, the thermal cut-out switches detect an overly hot condition, and shut down the triacs via signals on lines 552 or 554.
The main heater zone of the film heater is rated at 360 w&tts while the manifold and edge heater zones are rated at 180 watts and 170 watts respectively. The triac drivars are Motorola MAC 15A10 15 amp triacs. Each heater zone is split into 2 electrically isolated sections each dissipating 1/2 tht power. The 2 halves are connected in parallel for line voltages at Big less than 150 volts RMS. For line voltages groater than this, the two halves are connected in series.
These alternate connections are accomplished through a "personality- plug 550.
15 The AC power supply for the film heater zones is line 559, and the AC supply for the heated cover is via line 560.
*6 A zero' crossing detector $66 provides basic system i*ming by emitting a pulse on line 568 at each zero crolsing of the AC power on liane 518. The zero crossing detector i a National LX 311N referenced to analog ground and has 25 mV of hysteresis. The zero crossing detector takes its input from transformer 516 which outputs A.C. mignal from 0 to .o r5.52 volts for an A.C. input signal of from 0 to 240 volts
A.C.
A power transformer 570 supplies A.C. power to the pump 41 .0 tht- u powerlo t..o t°h o f that puzps coolant through the ramp and bias cooling &GV channels. The refrigeration unit 40 also receives its
A.C.
g 4, power from the transformer 570 via another portion of the j personality plug 550. The transformer 550 also supplies power to three regulated power supplies 572, 492 and 574 and one unregulated power supply 576.
For accuracy purposes, in measuring the tamperatures, the calibration voltage generator 506 uses a series of Very precise, thiln-film, ultralow temperature drift 20K ohm resistors (not shown in Figure 47 These same ultralow drift 85 resistors are used to set the gain of an analog amplifier D 578 which amplifies the output voltage from the selected temperature sensor prior to conversion to a digital value.
These resistors drift only 5 ppm/CO.
All the temperature sensors are calibrated by placing them (separated from the structures whose temperatures they measure) first in a stable, stirred-oil, temperature controlled bath at 40 0 C and measuring the actual output voltages at the inputs to the multiplexer 492. The temperature sensors are then placed in a bath at a temperature of 95 0 C and their output voltages are again' measured at the same points. The output voltage of the calibration voltage generator 506 is also measured at the *j input of the multiplexer 494. For each temperature, the 15 digital output difference from the A/D converter 486 between each of the temperature sensor outputs and the digital output that results from the voltage generated by the calibration voltage generator 506 is measured. The calibration constants for each temperature sensor to calibrate each for changes in temperature may then be calculated.
The sample block temperature sensor is then subjected to a further calibration procedure. This procedure involves driving the sample block to two different temperatures. At "5 each temperature level, the actual temperature of the block in 16 different sample wells is measured using 16-RTD thermocouple probes accurate to within 0.02 0 C. An average profile for the temperature of the block is then generated and the output of the A/D converter 464 is measured with the 30 block temperature sensor in its place in the sample block.
This is done at both temperature levels. From the actual block temperature as measured by the RTD probes and the A/D output for the block temperature sensor, a further calibration factor can be calculated. The temperature calibration factors so generated are stored in battery backed up RAM 458. Once these calibration factors are 86 determined for the syttm, it isi important that the sygtem not drift appreciably from the electrical characteristics "hat existed at the time of calibration. It is important therefore that low drift circuits be ftelectod and that ultralow drift-resistors be used.
The manner in which the CPU 450 controls the sample :block temperature can bo best Understood by reference to the secotion below describing the control program. However, to os...illustrate how the el. ;tronic- circuitry of Pigure .47 :.'cooperatec. with the control software to carry out a PCR protocol consider the following.
The zero crossing detector 566 has two outputs in output bus 568. one of these outputs emita a negative going pulse for every positive going transition of the A.C. signal: across the zero voltage reference. The other amitB a negative pulse upon every negative-going transition of ^thei A.C. signal across the zero reference voltage level. Thee .0:.20 two pulses, shown typically at 580 define one cotplete cycle or two half cycles. It is the pulse trains on bug 568 which dsfine the 200 millisecond sample periods. For 60 cycle/see A. C. an found in the 200 milliseconds contains 24_half Atc typical sample period is shown in Figure 49. Each "tc"mr0nFgr 9rpeet n half cycle. During each 200 msac sample period, the CP'U 450 is calculating the 41.ount of beating or cooling power needed to maintain the s 'ample block temperature at a user defined setpoint or incubation temperature or to move the block temperatuz-s to a new temperature depending upon where in the PCR protocol time line the particular sample period lies. The amiount of power needed in each film beater zone in converted into a number of halt cycles each heater zone is to remain off during the next 200 macc sample period. Juut before the end of the current sarpla period in which these calculation& ae 87 made, the CPU 450 addresses each of the 4 timers in the programmable interval timer (PIT) 472. To each timer, the CPU writes data constituting a "present" count representing the number of half cycles the heater zone associated with that timer is to remain off in the next sample period. In Figure 49, this data is written to the timers during interval 590 just preceding the starting time 592 of the next sample period. Assume that a rapid ramp up to the denaturation temperature of 94OC is called for by the user setpoint data for an interval which includes the sample S interval between times 592 and 594. Accordingly, the film heaters will be on for most of the period. Assume that the o"00. central zone heater is to be on for all but three of the half cycles during the sample period. In this case, the CPU 15 450 writes a three into the counter in PIT 472 associated with the central zone heater during interval 590. This write operation automatically causes the timer to issue a "shut off" signal on the particular control line of bus 592 which controls the central zone heater. This "shut off" .20 signal causes the PAL 484 to issue a "shut off" signal on the particular one of the signal lines in bus 538 associated with the central zone. The triac driver 530 then shuts off at the next zero crossing, at time 592. The PIT receives a pulse train of positive-going pulses on line 594 25 from the PAL 484. These pulses are translations of the zero-crossing pulses on 2-line bus 568 by PAL 484 -into positive going pulses at all zero crossing pulses on 2-line bus 568 by PAL 484 into positive going pulses at all zero crossings on a single line, line 594. The timer in PIT 472 associated with the central film heater zone starts counting down from its present count of 3 using the half cycle marking pulses on line 594 as its clock. At the end of the third half cycle, this timer reaches 0 and causes its output signal line on bus 592 to change states. This transition from the off to on state is shown at 596 in Figure 49. This transition is communicated to PAL 484 and 88 causes it to change the state of the appropriate output B signal on bus 538 to switch the triac driver 530 on at the third zero-crossing. Note that by switching the triacs on at the zero crossings as is done in the preferred embodiment, switching off of a high current flowing through an inductor (the film heater conductor) is avoided. This minimizes the generation of radio frequency interference or other noise. Note that the technique of switching a portion of eah half cycle to the film heater in accordance with the calculated amount of power needed will also work as an alternative embodiment, but is not preferred because of the noise generated by this technique.
The other timers of PIT 472 and 474 work in a similar manner to manage the power applied to the other heater zones V. 15 and to the heated cover in accordance with power calculated by the CPU.
Ramp cooling is controlled by CPU 450 directly through the peripheral interface 482. When the heating/cooling power calculations performed during each sample period 2. indicate that ramp cooling power is needed, the CPU 450 addresses the peripheral interface controller (PIC) 482. A data word is then written into the appropriate register to drive output line 600 high. This output line triggers a pair of monostable multivibrators 602 and 604 and causes ,o:25 each to emit a single pulse, on lines 606 and 6a18, respectively. These pulses each have peak currents just under 1 ampere and a pulse duration of approximately 100 milliseconds. The purpose of these pulses is to drive the solenoid valve coils that control flow through the ramp cooling channels very hard to turn on ramp cooling flow quickly. The pulse on line 606 causes a driver 610 to ground a line 612 coupled to one side of the solenoid coil 614 of one of the solenoid operated valves. The other terminal of the coil 614 is coupled to a power supply "rail" 616 at +24 volts DC from power supply 576. The one shot 602 controls the ramp cooling solenoid operted valve for flow in 89 w nne dllrantlnn, and1 the nne shnt ,fin& rhontrols the molenoid operated valve for flow .in the opposite direction.
Sixmultaneouslye the activation of thO RCOOL signal on 1U#rae 60o causes a driver 618 to be activated. This driver the line 612 through a current liviting resistor 620. The value of this current limiting resistor is such that the current flowing through line 622 is at least equl to the hold current necessary to keep the solenoid valve 614 open. Solenoi~d coils hava transient characterijstics that e 10 raquire large currents to turn on a solenoid operated valve but substantially loss current to keep the valve open.z When the 100 imsc pulse on line 606 subsidtal the driver 612 coases directly grounding the line 612 leaving only the ground connection through the resistor 620 and driver 618 for holding current.
The soltanoid valve 614 controls the flow of ramp cooling coolant through the xazplo block in only 1/2 the ramp cooling tubes, tubes carryi-ng the. coolant i-n one direction through the sample block. Another solenoid *20 oparatod valve 624 controls the coolant flow of coolant through the aamplt block in the opposite direction. This valve 624 is driven in exactly the same way as; solenoid operated valve 614 by drivers 626 and 628, one shot 604 and lino 608.7 The need for ramp cooling is evaluated once every sample period, When the PID task of the control software determines from measuring the block temperature and comparing it to the desired block temperature that ramp cooling is no longer needed, the iRCOOL signal on line soo is aeactivated. Thim is done by the CPU 450 by addressing the PIC 482 and writing data to it which reverse* the state of the appropriate bit in the register in 131C 482 which is coupled to line 600.
90 The PIT 474 also has two other timers therein which time a 20 Hz interrupt and a heating LED which gives a viscible indication when the sample block is hot and unsafe to touch.
The system also includes a beeper one shot 630 and a beeper 632 to warn the user when an incorrect keystroke has been made.
The programmable interrupt controller 476 is used to detect 7 interrupts; Level I- test; Level 2-20 Hz; Level 3 Transmit Ready; Level 4 Receive ready; Level 5 Keyboard interrupt; Level 6 Main heater turn on; and, Level 7 A.C. line zero cross.
The peripheral interface controller 482 has four :15 outputs (not shown) for controlling the multiplexers 492 and 494. These signalt MUXI EN and MUX2 EN enable one or the other of the two multiplexers 492 and 494 while the signals MLX 0 and,-MUX 1 control which- channel is selected for input to the amplifier 578. These signals are managed so that 20 only one channel from the two multiplexers can be selected at any one time.
An RLTRIG* signal resets a timeout one shot 632 for the heaters which disables the heaters via activation of the ignal TIMEOUT EN* to the PAL 484 if the CPU crashes.--That 25 is, the one shot 632 has a predetermined interval which it will wait after each trigger before it activates the signal TIMEOUT EN* which disables all the heater zones. The CPU 450 executes a routine periodically which addresses the PIC 482 and writes data to the appropriate register to cause activation of a signal on line 634 to trigger the one shot 632. If the CPU 450 "crashes" for any reason and does not execute this routine, the timeout one-shot 632 disables all the heater zones.
The PIC 482 also has outputs COVHTR EN* and BLJKHTREN* (not shown) for enabling the heated cover and the sample block heater. Both of these signals are active low and are 91 controlled by the CPU 450. They are output to the PAL 484 via bus 636.
The PIC 482 also outputs the signals BEEP and BEEPCLR* on bus 640 to control the beeper one shot 630.
The PIC 482 also outputs a signal MEM1 (not shown) which is used to switch pages between the high address section of EPROM 456 and the low address section of battery RAM 458. Two other signals PAGE SEL 0 and PAGE SEL 1 (not shown) are output to select between four 16K pages in EPROM 456.
The four temperature sensors are National LM 135 zener diode type sensors with a zener voltage/temperature dependence of 10 mV/*K. The zener diodes are driven from S the regulated power supply 498 through the 20K resistor 496.
15 The current through the zeners varies from approximately 560 AA to 615 AA over the OOC to 100 0 C operating range. The zener self heating varies from 1.68 mW to 2.10 mW over the same range.
The multiplexers 492 and 494 are DG409 analog switches.
The voltages on lines 488 and 490 are amplified by an AD625KN instrumentation amplifier with a transfer function of Van= 3*Vl, 7.5. The A/D converter 486 is an AD7672 with an input range from 0-5 volts. With the zener temperature sensor output from 2.73 to 3.73 volts over the 0OC to 100 0
C
25 range, the output of the amplifier 578 will be 0.69 volts to 3.69 volts, which is comfortably within the A/D input range.
The key to highly accurate system performance are good accuracy and low drift with changes in ambient temperature.
Both of these goals are achieved by using a precision voltage reference source, calibration voltage generator 506, and continuously monitoring its output through the same chain of electronics as are used to monitor the outputs of the temperature sensors and the AC line voltage on line 510.
The calibration voltage generator 506 outputs two precision voltages on lines 650 and 652. One voltage is 92 3.75 volts and the ether in 3.125 volts. These Voltages are obtained by dividing down a regulated supply voltage using a string of ultralow drift, inteqrated, thin fi.lm resistors with a 0.054 match between retistors and a 5 ppm/degiree c temperature drift coefficient between resistors. The calibration voltage generator also qgemerates -5 volts; for the A/D converter refearence voltage and -7.5 volts for the instrumentation amplifier offset. These two voltages are commnunicated to the A/D 486 and the amplifier 578 by lines .0 which are not shown. These two negative voltages are generated using the samie thin film rosistor network and OP *27 GZ op-amps (not shown), The gain setting resistors for the operational. amplifier 578 are also the ultraleow drift, thin-film, integrated, matched resistors.
The control firmware, control electronics and the block design are designed such that well-to-well and instrumentto-instrument transportability of PCR protocolit in possible.
High throughput laboratories benefit from instrumentjs- C which are easy to use for a wide spectrum of lab personnel 2 and which requ~ire a minimal amount of training. The toftware for tha invention was developed to handle complex VCR thermocycling protocol* while remaining easy to program.
In addition, it is provided with safeguards to assure. the inltegrity of samples during power interruptions, and can document the detailed events of each rum in safe inamory, After comploting power-up self-checks shown in Figures 53 and 54, to assure the operator that the system in operating properly, the user interface of the invention offers a simple, top-level imenu, inviting the user to rune create or edit a tile, or to ticcess a utility function. No programming skills are required, since pro-existing default file& can be quickly edited with customized times and temperatures, then stored in memory for later Use. A file protection schaze prevents unauthorized chan~ges to any user's programs, A file nor-mally conaists of a set of instructions to hold a desired 93 O temperature or to thermocycle. Complex programs are created by linking files together to form a method. A commonly used file, such as a 40C incubation following a thermocycle, can be stored and then incorporated into methods created by other users. A new type of file, the AUTO file is a PCR cycling program which allows the user to specify which of several types of changes to control parameters will occur each cycle: time incrementing (auto segment extension, for yield enhancement), time decrementing, or temperature incrementing or decrementing. For the highest degree of Scontrol precision and most reliable methods transferability, temperatures are setable to 0.1 0 C, and times are programmed to the nearest second. The invention has the ability to program a scheduled PAUSE at one or more setpoints during a 15 run for reagent additions or for removal of tubes at specific cycles.
The system of the invention has the ability to store a 500 record history file for each run. This feature allows the user to review the individual steps in each cycle and to 20 flag any special status or error messages relating to irregularities. With the optional printer, the invention provides hardcopy documentation of file and method parameters, run-time time/temperature data with a time/date stamp, configuration parameters, and sorted file 25 directories.
In order to assure reproducible thermocycling, the computed sample temperature is displayed during the ramp and hold segments of each cycle. A temperature one degree lower than the set temperature is normally used to trigger the ramp-time and hold-time clocks, but this can be altered by the user. Provided the proper time constant for the type of tube and volume is used, the sample will always approach the desired sample temperature with the same accuracy, regardless of whether long or short sample incubation times have been programmed. Users can program slow ramps for the specialized annealing requirements of degenerate primer 94 pools, or very short (1-5 sac) high -temperatur~e denaturation per~iods for vetry GC r~ich targets. Intelligent defaults are preprogrammesd for 2- and 3-temperature PCR cycles.
Diagnostic tests can be accossed by any users to chock the heating and cooling system status, zince the software gives Pact/Fail reports. in addition, a system performance program performs a comprehensive subsystem evaluation and gehgratss a summary status raport.
S SThe control firmware is comprisad of several sections IQ t which are listed below; Diagnostics -Calibration install Real time operating systemn ine prioritized tasks that manage the system Start-up sequence 0*g* Usger interface S The various sections of the firmware will be described with either textual description, pseudooode or both.
Features of the firmware are: 1. A Control system that manages the *arage sample block temperature to within 0-16C as well as maintaining the temperature non-unifcz-mi ty an between wells in the sample block to within 1 0 .59C.
2. A temperature control system that iaeasu.r1Hj and compensates. for line voltage fluctuations and~ electronic temperature drift.
95
S
10 0 0 0 0 0e 3. Extensive power up diagnostics that determine if system components are working.
4. Comprehensive diagnostics in the install program which qualify the heating and cooling systems to insure they are working properly.
A logical and organized user interface, employing a menu driven system that allows instrument operation with minimal dependency on the operators manual.
6. The ability to link up to 17 PCR protocols and store them as a method.
7. The ability to store up to 150 PCR protocols and methods in the user interface.
8. A history file--that records up to 500 events ofthe previous run as part of the sequence task.
9. The ability to define the reaction volume and tube size type at the start of a run for maximum temperature accuracy and control as part of the user interface and which modifies tau (thetube time constant) in the PID task.
Upon recovery from a power failure, the system drives the sample block to 40C to save any samples that may be loaded in the sample compartment. The analyzer also reports the duration of the power failure as part of the sequence task.
11. The ability to print history file contents, "run time" parameters and stored PCR protocol parameters as part of the print task.
95A 12. The ability to configure to which the apparatus will return during any idle state.
13.. The ability to check that the set point temperature is reached with a reasonable amount of time.
14. The ability to control the instrument remotely via an RS232 port.
*0 96 There are several levels of diagnostics which are described below: A series of power-up tests are automatically performed each time the instrument is turned on. They evaluate critical areas of the hardware without user intervention.
Any test that detects a component failure will be run again.
If the test fails twice, an error message is displayed and the keyboard is electronically locked to prevent the user from continuing.
The following areas are tested: Programmable Peripheral Interface device Battery RAM device Battery RAM checksum EPROM devices "15 Programmable Interface Timer devices S. Clock Calendar device Programmable Interrupt Controller device Analog to Digital section Temperature sensors 20 Verify proper configuration plug A Series of service only diagnostics are available to final testers at the manufacturer's location or to field service engineers through a "hidden" keystroke sequence unknown to the customer). Many of the tests are-the 25 same as the ones in the start up diagnostics with the exception that they can be continually executed up to 99 times.
The following areas are tested: Programmable Peripheral Interface device Battery RAM device Battery RAM checksum EPROM devices Programmable Interface Timer devices 97 Clock Calendar device Programmable Interrupt Controller device Analog to Digital section RS-232 section Display section Keyboard Beeper Ramp Cooling Valves Check for EPROM mismatch Firmware version level Battery RAM Checksum and Initialization Autostart Program Flag Clear Calibration Flag 00•0 Heated Cover heater and control circuitry .15 Edge heater and control circuitry Manifold heater and control circuitry Central heater and control circuitry Sample block thermal cutoff test Heated cover thermal cutoff test 0e 20 User diagnostics are also available to allow the user S to perform a quick cool and heat ramp verification test and an extensive confirmation of the heating and cooling system.
These diagnostics also allow the user to view the history o o file, which is a sequential record of events that occurred oo. 25 in the previous run. The records contain time, temperature, V setpoint number, cycle number, program number and status messages.
Remote Diagnostics are available to allow control of the system from an external computer via the RS-232 port.
Control is limited to the service diagnostics and instrument calibration only.
Calibration to determine various parameters such as heater resistance, etc. is performed. Access to the calibration screen is limited by a "hidden" key sequence unknown to the customer). The following parameters 98 are calibrated: The configuration plug is a module that rewires the chiller unit, sample block heaters, coolant pump and power supplies for the proper voltage and frequency (100V/50Hz, 100/60Hz, 120/60Hz, 220/50Hz or 230/50Hz). The user enters the type of configuration plug installed. The firmware uses this information to compute the equivalent resistance of the sample block heaters. Upon power-up, the system verifies that the configuration plug selected is consistent with the current line voltage and frequency.
The heater resistance must be determined in the calibration process so that precise calculations of heater power delivered can be made. The user enters the actual resistances of the six sample block heaters (two main *o15 heaters, two manifold heaters and two edge heaters). The configuration plug physically wires the heater in series for S220-230 VAC and in parallel for 100-120 VAC operation. The firmware computes the equivalent resistance of each of the three heaters by the following formula: For 100-120 VAC: R,
R
2 R, R For 220-230 VAC: Re R, R 2 The equivalent resistance is used to deliver a precise amount of heating power to the sample block (Power Voltage 2 S x Resistance).
25 The calibration of the A/D circuit is necessary so that temperatures can be precisely measured. This is performed by measuring two test point voltages (TP6 and TP7 on the CPU board) and entering the measured voltages. The output of the A/D at each voltage forms the basis of a two point calibration curve. These voltages are derived from a 5 volt precision source and are accurate and temperature independent. At the start of each run, these voltages are read by the system to measure electronic drift due to 99 O temperature because any changes in A/D output is due to temperature dependencies in the analog chain (multiplexer, analog amplifier and A/D converter).
Calibration of the four temperature sensors (sample block, ambient, coolant and heated cover) is performed for accurate temperature measurements. Prior to installation into an instrument, the ambient, coolant, and heated cover temperature sensors are placed in a water bath where their output is recorded (XX.XOC at YYYY mv). These values are then entered into the system. Since temperature accuracy in these areas is not critical, a one point calibration curve is used.
The sample block sensor is calibrated in the S. instrument. An array of 15 accurate temperature probes is •15 strategically placed in the sample block in the preferred embodiment. The output of the temperature probes is o collected and averaged by a computer. The firmware commands the block to go to 40 0 C. After a brief stabilizing period O the user enters the average block temperature as read by the 0 15 probes. This procedure is repeated at 950C, forming a two point calibration curve.
Calibration of the AC to DC line voltage sampling circuit is performed by entering into the system the output of the AC to DC circuit for two given AC input voltages, forming a two point calibration curve. The output of the circuit is not linear over the required range (90 260 VAC) and therefore requires two points at each end (100 and 120, 220 and 240 VAC), but only uses one set based on the current input voltage.
30 An accurate measure of AC voltage is necessary to deliver a precise amount of power to the sample block (Power Voltage 2 x Resistance).
The Install program is a diagnostic tool that performs an extensive test of the cooling and heating systems.
Install measures or calculates control cooling conductance, ramp cooling conductance at 10 0 C and 18 0 C, cooling power at 100 and 200C, sample block thermal and coolant capacity and sample block sensor lag. The purpose of install is three fold: 1. To uncover marginal or faulty components.
2. To use some of the measured values as system constants stored in battery backed up RAM to optimize the control system for a given instrument.
3. To measure heating and cooling system degradation over time
S
Install is executed once before the system is shipped oo and should also be run before use or whenever a major component is replaced. The Install program may also be run by the user under the user diagnostics.
0.0o 15 The heater ping test- verifies that the heaters are so properly configured for the current line voltage in parallel for 90-132 VAC and in series for 208-264 VAC). The firmware supplies a burst of power to the sample block and then monitors the rise in temperature over a 10 second time period. If the temperature rise is outside a specified ramp rate window, then the heaters are incorrectly wired for the current line voltage and the install process is terminated.
The control cooling conductance tests measures the thermal conductance K^ across the sample block to the control cooling passages. This test is performed by first driving the sample block temperature to 600C (ramp valves are closed), then integrating the heater power required to maintain the block at 60 0 C over a 30 second time period.
The integrated power is divided by the sum of the difference between the block and coolant temperature over the interval.
101 S T K, Z Heater Power 60c E Block Coolant Temp Typical values are 1.40 to 1.55 Watts/oC. A low KC may indicate a clogged liner(s). A high may be due to a ramp valve that is not completely closed, leakage of the coolant to the outside diameter of the liner, or a liner that has shifted.
The block thermal capacity (Blk Cp) test measures the thermal capacity of the sample block by first controlling the block at 35 0 C then applying the maximum power to the heaters for 20 seconds. The block thermal capacity is equal to the integrated power divided by the difference in block temperature. To increase accuracy, the effect of bias cooling power is subtracted from the integrated power.
(10) Blk Cp ramp time (heater control cool pwr) i. delta temp.
where: ramp time 20 seconds heater power 500 watts control cool (E block coolant temp) delta temp TBlockt.
20 TBlockt.- 0* 0 The typical value of Block Cp is 540 watt-seconds/oC Assuming a normal KC value, an increase in block thermal capacity is due to an increase in thermal loads, such as moisture in the foam backing, loss of insulation around the sample block, or a decrease in heater power such as a failure of one of the six heater zones or a failure of the electronic circuitry that drives the heater zones, or an incorrect or an incorrectly wired voltage configuration module.
102 A chiller test measures the system cooling output in watts at 100C and 180C. The system cooling power, or chiller output, at a given temperature is equal to the summation of thermal loads at that temperature. The main components are: 1. heating power required to maintain the block at a given temperature, 2. power dissipated by the pump used to circulate the coolant around the system, and 3.
losses in the coolant lines to the ambient. The chiller power parameter is measured by controlling the coolant temperature at either 100C or 180C and integrating the power applied to the sample block to maintain a constant coolant temperature, over a 32 second interval. The difference between the block and coolant temperature is also integrated to compute losses to ambient temperature.
(11) Chiller power Z Heating power Pump power (Kamb Z (blk-cool temp)) where: heating power Sum of heating power required to maintain coolant at 10 0
C
or 180C over time 32 seconds.
Pump Power Circulating pump, 12 watts Kamb Conductance to ambient, watts/OC blk-cool temp Sum of difference in block 5 and coolant temp over time 32 seconds The typical value for chiller power is 230 watts S at 100C and 370 watts 30 at 18 0 C. Low chiller power may be due to an obstruction in the fan path, a defective fan, or a marginal or faulty chiller unit. It may also be due to a miswired voltage configuration plug.
A ramp cooling conductance test measures the thermal conductance at 10 0 C and 18 0 C across the sample block 103 S to the ramp and control cooling passages. This test is performed by first controlling the coolant temperature at or 18 0 C, then integrating, over a 30 second time interval, the heating power applied to maintain the coolant at the given temperature divided by the difference of block and coolant temperature over the time interval.
(12) K c Z Heating power z (block coolant temperature) Typical values for K C are 28 watts/oC 3 at 10 0 C and 31 watts/OC 3 at 18 0 C. A low KC may be due to a closed or obstructed S: ramp valve, kinked coolant tubing, weak pump or a hard water/Prestone" mixture.
*000 V. A sensor lag test measures the block sensor lag by first controlling the block temperature to 35C and then applying 500 watts of heater power for 2 seconds and;measuring the time required for the block to rise 1 0
C.
Typical values are 13 to 16 units, where each unit is equal to 200 ms. A slow or long sensor lag can be due to a poor interface between the sensor and the block, such as lack of 00 thermal grease, a poorly machined sensor cavity or a faulty sensor.
The remaining install tests are currently executed by the install program but have limited diagnostic purposes due to the fact that they are calculated values or are a function of so many variables that their results do not determine the source of a problem accurately.
The install program calculates the slope of the ramp cooling conductance (Sc) between 180C and 10*C. It is a measure of the linearity of the conductance curve. It is also used to approximate the ramp cooling conductance at 0°C. Typical values are 0.40 0.2. The spread in values attest to the fact that it is just an approximation.
104 p (13) s c (Kc_180 Kc_10) (18oC 100C) The install program also calculates the cooling conductance
K
0
K
0 is an approximation of the cooling conductance at 0oC. The value is extrapolated from the actual conductance at 100C. Typical values are 23 watts/oc 5. The formula used is: (14) Ko 0 Kc_10 (Sc 100C) The install program also calculates coolant capacity (Cool Cp) which is an approximation of thermal capacity of the entire coolant stream (coolant, plumbing lines, heat exchanger, and valves). The cooling capacity is equal to components that pump heat into the coolant minus the components that remove heat from the coolant. The mechanics used to measure and calculate these components are complex and are described in detail in the source code description section. In-this measurement; the coolant is allowed to stabilize at 100c. Maximum heater power is applied to the sample block for a period of 128 seconds.
(15) Cool Cp Heat Sources Coolant sources 0* :20 (16) Cool Cp Heater Power Pump Power Kamb (ZTamb ZTcool) Block Cp (Tblockto Tblockt,, 8 Average Chiller Power between Tcoolt.
0 and Tcool,2 Characters enclosed in indicate the variable names used in the source code.
Heater-Ping Test Pseudocode: The heater ping test verifies that the heaters are properly wired for the current line voltage.
105 Get the sample block and coolant to a known and stable point.
Turn ON the ramp cooling valves Wait for the block and coolant to go below 56C Turn OFF ramp cooling valves Measure the cooling effect of control cooling by measuring the block temperature drop over a 10 second time interval. Wait 10 seconds for stabilization before taking any measurements.
Wait 10 seconds templ block temperature Wait 10 seconds temp2 block temperature o* {tempa} temp2 templ 15 Examine the variable {linevolts} which contains the actual measured line voltage. Pulse the heater with watts for a line voltage greater then 190V or with 300 watts if it less than 140V.
if ({linevolts} 190 Volts) then deliver 75 watts to heater else deliver 300 watts to heater Measure the temperature rise over a 10 second time period. The result is the average heat rate in 0.01 *25 0 /second.
templ block temperature Wait 10 seconds temp2 block temperature {tempb} temp2 templ 106 O Subtract the average heat rate {tempb} from the control cooling effect to calculate true heating rate (17) heat_rate {tempb} {tempa} Evaluate the heat rate. For 220V-230V, the heat rate should be less than 0.30 O/second. For 100V-120V the heat rate should be greater than 0.30 "/second.
if (linevoltage 220V and heat_rate 0.30 °/second) then Error Heaters wired for 120 Lock up keyboard if (linevoltage 120V and heatrate 0.30 */second) then *6 Error Heaters wired for 220 Lock up keyboard *0 ,*.015 KCC Test Pseudocode: This test measures the control cooling conductance also known as KC.
Kcc is measured at a block temperature of *a 0 Drive block to 600C 20 Maintain block temperature at 60 0 C for 300 seconds S* Integrate the power being applied to the sample block heaters over a 30 second time period. Measure and integrate the power required to maintain the block temperature with control cooling bias.
{dt_sum} 0 (delta temperature sum) {main_pwrsum} 0 (main heater power sum) {aux_pwr_sum} 0 (auxiliary heater power sum) for (count 1 to S -107 {dtsu} dt-suml (block temperature coolant temperature) Wait 1 sec Accumulate the power applied to the main and &UXiliary heaters. The actual code resides in the PID. Control task and is therefore sumned every 200ms, (xai~pwrst {Nainpwr~sum) {&ctu&lpoweri {auxJpwr5su} faux_;pqrsau= auxl-actuall .:{Ux2 actual) Compute: the conductance~ by dividing the power sun by the temperature sum. Note that the units are 10 mfw/ac.
1(1s) Kre ({mainjpwrsumj jauxjpwr_um}) dtsm BLOC "PTs su Ode: This test measures the sampl~e block thermal capacity.
Drive the block to 359C Control block temperature at 35 0 C for 5 seconds and 2Qrecord initial temaperature.
initia-tamp block temperature Deliver maximum power to heaters for 20 seconds while summing the difference in block to coolant temperature as well an heater power.
Deliver s00 watts {dt-sum} o 0 108 for (count 1 to 20 seconds)
S{
dtsum {dtsum} (block temperature coolant temperature) wait 1 second (19) delta_temp block temperature initialtemp Compute the joules in cooling power due to control cooling which occurs during ramp.
*.10 (20) cool joule Control cooling conductance (K {dt sum} SCompute the total joules applied to the block from the main heater and control cooling. Divide by temp change over the interval to compute thermal capacity.
(21) Block CP ramptime (heater power cooljoule) /delta temp where: ramptime 20 seconds S. heater power 500 Watts
CC
S COOLPWR E* o 0 This test measures the chiller power at Control the coolant temperature at 10 0 C and stabilize for 120 secs.
count 120 do while (count 0) if (coolant temperature 10 0.5cC) then 109 count count 1 else count 120 wait 1 second At this point, the coolant has been at 100C for 120 seconds and has stabilized. Integrate, over 32 seconds, the power being applied to maintain a coolant temperature of 10 0
C.
10o {cool init} coolant temperature {mainpwr_sum} 0 *see {aux_pwr_sum} 0 {delta temp sum} 0 0 0 for (count 1 to 32) Accumulate the power applied to the main andauxiliary heaters. The actual code resides in the control task.
{mainpwr sum} {main_pwr_sum} actual_power {aux_pwr sum} {aux_pwr_sum} auxl_actual aux2 actual delta_temp_sum delta_temp_sum (ambient temp coolant temp) wait I second Compute the number of joules of energy added to the coolant mass during the integration interval. "(coolant temp cool_init)" is the change in coolant temp during the integration interval. 550 is the Cp of the coolant in joules, thus the product is in joules. It represents the extra heat added to the coolant which made it drift 110 9 from setpoint during the integration interval. This error is subtracted below from the total heat applied before calculating the cooling power.
(22) cool_init (coolant temp cool_init) 550J Add the main power sum to the aux heater sum to get joules dissipated in 32 seconds. Divide by 32 to get the average joules/sec.
(23) {main_pwr_sum} ({main_pwr_sum}+{aux_pwr_sum} coolinit) 32 Compute the chiller power at 10C by summing all the chiller power components.
(24) Power, 0 main_power_sum PUMP PWR (K AMB delta_temp_sum) where: 15 {main_pwr_sum} summation of heater power over interval PUMP PWR 12 Watts, pump that circulates coolant delta_temp_sum summation of amb coolant over interval K_AMB 20 Watts/K, thermal conductance from cooling to ambient.
KC 10 Test Pseudocode: This test measures the ramp cooling conductance at 10 0
C.
Control the coolant temperature at 10 0 C 0.5 and allow it to stabilize for 10 seconds.
At this point, the coolant is at setpoint and is being 111 O controlled. Integrate, over a 30 second time interval, the power being applied to the heaters to maintain the coolant at 10oC. Sum the difference between the block and coolant temperatures.
{main_pwr sum} 0 {aux_pwr_sum} 0 {dt_sum} 0 for (count 1 to 10 Accumulate the power applied to the main and auxiliary heaters. The actual code resides in the PID control task.
{main_pwr_sum) {main_pwr_sum} actual power {aux_pwr_sum} {aux_pwr_sum} auxlactual aux2_actual {dt_sum} {dt_sum} (block temperature coolant o* temp) 0 wait 1 second :.,o20 Compute the energy in joules delivered to the block over the summation period. Units are in 0.1 watts.
{main_pwr_sum} {mainpwr_sum} {aux pwr_sum} Divide the power sum by block coolant temperature sum to get ramp cooling conductance in 100 mW/K.
(26) Kcl0 {main_pwr_sum} {dt_sum} COOL PWR 18 Test Pseudocode: 112 This test measures the chiller power at 18 0 C Get the sample block and coolant to a known and stable point. Control the coolant temperature at 18oC and stabilize for 128 secs.
count 128 do while (count 0) if (coolant temperature 180C 0.5) then count count 1 *10 else count 120 wait 1 second At this point the coolant has been at 18 0 C for 120 seconds and has stabilized. Integrate, over 32 seconds, the power being applied to maintain a coolant temperature of 18 0
C.
.s {cool_init} coolant temperature a {main_pwr_sum} 0 20 {aux_pwr_sum} 0 {delta_temp_sum} 0 for (count 1 to 32) 0040 4 0 Accumulate the power applied to the main and auxiliary heaters. The actual code resides in the control task.
{main_pwr_sum) {main_pwrsum} actualpower {aux_pwr_sum) {aux_pwr_sum} auxl_actual aux2_actual 113 delta-tempsum delta_temp_sum (ambient temp coolant temp) wait I second Compute the number of joules of energy added to the coolant mass during the integration interval. "(coolant temp cool init)" is the change in coolant temp during the integration interval. 550 is the Cp of the coolant in joules, thus the product is in joules. It represents :.10 the extra heat added to the coolant which made it drift setpoint during the integration interval. This error is 0subtracted below from the total heat applied before 0*7* calculating the cooling power.
a (27) cool init (coolant temp cool init) 550 Add main power sum to aux heater sum to get joules dissipated :.n32 seconds. Divide by 32 to get the average joules/sec.
(28) (main_pwr_sum) ({main_pwr_sum}+{auxpwr_sum) coolinit) 32 Compute the chiller power at 18 0 C by summing all -the chiller power components.
(29) Powere.c main_power_sum PUMP PWR (K AMB deltatempsum) where: mainpwr_sum} summation of heater power over interval PUMP PWR 12 Watts, pump that circulates coolant deltatemp_sum summation of amb coolant over 114 O interval K_AMB 20 Watts/K, Thermal conductance from cooling to ambient.
KC 18 Test Pseudocode: This test measures the ramp cooling conductance at 18 0
C.
Control the coolant temperature at 180C 0.5 and allow it to stabilize for 10 seconds.
At this point, the coolant is at setpoint and being controlled. Integrate, over a 30 second time interval, the power being applied to the heaters to maintain the coolant at 18 0 C. Sum the difference between the block and coolant temperature.
{main_pwr_sum} 0 15 {aux_pwr_sum} 0 o* {dt_sum} 0 for (count 1 to Accumulate the power applied to the main and auxiliary heaters. The actual code resides in the control task.
{mainpwr_sum} {main_pwr_sum} actual power {aux_pwr_sum} {aux_pwr_sum} auxl actual aux2_actual 25 {dt sum} {dt_sum} (block temperature coolant temp) wait 1 second 115 O Compute the energy in joules delivered to the block over the summation period. Units are in 0.1 watts.
{mainpwr_sum} {mainpwr_sum} {aux_pwr_sum} Divide power sum by block coolant temperature sum to get ramp cooling conductance in 100 mW/K.
(31) Kc_18 {mainpwr_sum} {dt_sum} SENLAG Test Pseudocode: This test measures the sample block sensor lag.
Drive the block to 356C. Hold within 0.2°C for :10 seconds then record temperature of block.
o• oo {tempa} block temperature Deliver 500 watts of power to sample block.
Apply 500 watts of power for the next 2 seconds and count the amount of iterations through the loop for the block temperature to increase 10C. Each loop iteration executes every 200 ms, therefore actual sensor lag i-s equal to count 200 ms.
secs 0 00: count 0 do while (TRUE) if (secs 2 seconds) then shut heaters off if (block temperature tempa 1.0oC) then exit while loop 116 O count count 1 end do while sensor lag count Coolant CP Test Pseudocode: This test computes the coolant capacity of the entire system.
Stabilize the coolant temperature at 100C Send message to the PID control task to ramp the coolant temperature from its current value (about 100C) to 18 0
C.
Wait for the coolant to cross 12oC so that the coolant
CP
ramp always starts at the same temperature and has clearly started ramping. Note the initial ambient and block temperatures.
15 do while (coolant temperature 12 0
C)
wait 1 second {blk delta} block temperature {h2odelta} coolant temperature For the next two minutes, while the coolant temperature is ramping to 18C, sum the coolant temperature and the difference between the ambient and coolant temperatures.
{temp_sum} 0 {cool sum} 0 117 (32) 5(33) for (count 1 to 128 seconds) fcoolum) cool temp sum coolant temperature.
{temfp-sum) ambient coolant temperature wait 1 second count count 1 Calculate the change in temperatures over the two minute period.
(34) {blk -delta} block temperature {blk -delta) {h2o-delta) =coolant temperature {h2o-deltaj 0 0 S 00 9 0006 *0 0 0 00 0 Compute KChill, the rate of change of chiller power with coolant temperature over the coolant range of 10 0
C
to 20 0 C. Note that units are in watts/100C.
(36) Kchill =(Chiller Pwr 18 0 C Chiller Pwr 10 0
C)
Compute Sc which is the slope of the ramp cooling conductivity versus the temperature range of 180C to 10 0 C. The units are in watts/10 0 (37) SC- (Kc_18 KclO0) 8 Compute Kc_0, the ramp cooling conductance extrapolated to 0OC.
(38) Kc_0 KclO0 (Sc Compute Cp_Cool, the Cp of the coolant by: (39) CPCool 25 pCol HEATPOWER 128 PUMP PWR 128 118 Power 0 0 C 128 BlockCp blkdelta K_AMB temp sum Kchill cool_temp sum h2o delta where: HEATPOWER 0 a5
S.
S.
PUMP PWR Pwr 0OC 500 W, the heater power applied to warm the block, thus heating the coolant.
It is multiplied by 128, as the heating interval was 128 secs.
12 W, the power of the pump that circulates the coolant multiplied by 128 seconds.
The chiller power at 0 0 C multiplied by 128 seconds.
BlockCp Thermal capacity of sample block.
blkdelta *5 62 @5
S
K AMB temp_sum h2o delta Change in block temp over the heating interval.
20 Watts/K, thermal conductance from cooling to ambient.
The sum once per second of ambient coolant temperature over the interval.
Change in coolant temperature over interval of heating (approximately 6.C).
Slope of chiller power versus coolant Kchill 119 temp.
Cool-sum -The sum of coolant temp, once per second, over the heating interval.
0@ *00 so 0 120 9 REAL TIME OPERATING SYSTEM CRETIN CRETIN is a stand alone, multitasking kernel that provides system services to other software modules called tasks. Tasks are written in the language with some time critical areas written in Intel 8085 assembler. Each task has a priority level and provides an independent function.
CRETIN resides in low memory and runs after the startup diagnostics have successfully been executed.
CRETIN handles the task scheduling and allows only-one task to run at a time. CRETIN receives all hardware interrupts thus enabling waiting tasks to run when the proper interrupt is received. CRETIN provides a real time clock to allow tasks to wait for timed events or pause for known intervals. CRETIN also provides intertask communication through a system of message nodes.
The firmware is composed of nine tasks which are briefly described in priority order below. Subsequent sections will describe each task in greater detail.
1. The control task (PID) is responsible for controlling the sample block temperature.
2. The keyboard task is responsible for processing keyboard input from the keypad.
S 3. The timer task waits for a half second hardware interrupt, then sends a wake up message to both the sequence and the display task.
000 4. The sequence task executes the user programs.
The pause task handles programmed and keypad pauses 121 when a program is running.
6. The display task updates the display in real time.
7. The printer task handles the RS-232 port communication and printing.
8. The LED task is responsible for driving the heating LED. It is also used to control the coolant temperature while executing Install.
9. The link task starts files that are linked together in a method by simulating a keystroke.
S
o..
gO* *o
*S*
e* 122 Block Temperature Control Program (PID Task) The Proportional Integral Differential (PID) task is responsible for controlling the absolute sample block temperature to 0.1C, as well as controlling the sample block temperature non-uniformity (TNU, defined as the temperature of the hottest well minus the temperature of the coldest well) to less than 0.5 0 C by applying more heating power to the perimeter of the block to compensate for-losses through the guard band edges. The PID task is also responsible for controlling the temperature of the heated cover to a less accurate degree. This task runs 5 times per second and has the highest priority.
The amount of heating or cooling power delivered to the sample block is derived from the difference- or "error" between the user specified sample temperature stored in memory, called the setpoint, and the current calculated sample temperature. This scheme follows the standard loop control practice. In addition to a power contribution to the film heaters directly proportional to the current error, the proportional component, (setpoint temperature minus sample block temperature), the calculated power also incorporates an integral term that serves to close out any static error (Setpoint temperature Block temperature less 25 than 0.50C). This component is called the integral component. To avoid integral term accumulation or "windup", contributions to the integral are restricted to a small o* band around the setpoint temperature. The proportional and integral component gains have been carefully selected and tested, as the time constants associated with the block sensor and sample tube severely restrict the system's phase margin, thus creating a potential for loop instabilities.
The proportional term gain is P in Equation (46) below and the integral term gain is Ki in Equation (48) below.
123 The PID task uses a "controlled overshoot algorithm"r where the block temperature often overshoots its final steady state value in order for the sample temperature to arrive at its desired temperature as rapidly as possible.
The use of the overshoot algorithm causes the block temperature to overshoot in a controlled manner but does not cause the sample temperature to overshoot. This saves power and is believed to be new in PCR instrumentation.
The total power delivered to all heater of the sample block to achieve a desired ramp rate is given by: Power =(CP ramp_rate) bias where: eC.. c= Thermal mass of block *bias bias or control cooling power 15 ramp_rate Tfia Tinitist desired ramp rate This power is clamped to a maximum of 500 watts of heating power for safety.
a. *With every iteration of the task (every 200ms)- the e system applies heating or ramp cooling power (if necessary) based on the following algorithms.
CC The control system is driven by the calculated sample a temperature. The sample temperature is defined as the average temperature of the liquid in a thin walled plastic sample tube placed in one of the wells of the sample block (herafter the "block"). The time constant of the system (sample tube and its contents) is a function of the tube type and volume. At the start of a run, the user enters the tube type and the amount of reaction volume. The system 124 computes a resultant time constant (r or tau). For the MicroAmp*' tube and 100 microliters of reaction volume, tau is approximately 9 seconds.
(41) Tbik. TbLk Power (200ms CP) (42) T-ne Ts, (Tbtk. 200ms tau where: Tbtk-new Current block temperature Tbk Block temperature 200ms ago Power Power applied to block CP Thermal mass of block TgMp-w Current sample temperature TP Sample temperature 200ms ago tau Thermal Time Constant of sample for sensor lag (approximately
C
S B 4* *400 4 4009 4 '-mm em 4 *94 Be..
0 4.
4* 4~ me..
me 4* S em m 9 me 0 .0500.
S
tube, adjusted The error signal or temperature is simply: error Setpoint T.r..
(43) As in any closed loop system, a corrective action (heating or cooling power) is applied to close out- part of the current error. In Equation (45) below,F is the fraction 20 of the error signal to be closed out in one sample period (200mS).
(44) TV. T, F (SP T wew e 0 h where SP the user setpoint temperature Due to the large lag in the system (long tube time constant), the fraction F is set low.
Combining formulas (42) and (44) yields: 125 T -r (SP-Temp) Ta (TbI.new--T .2 tau Ts F Combining formulas (41) and (45) and adding a term P (the proportional term gain) to limit block temperature oscillations and improve system stability yields: (46) Pwr CP P/T ((SP T F tau/T T Tbk) S&V Sm bp where
P
T
and P/T the proportional term gain and the sample period of 0.2 seconds (200 msec).
1 in the preferred embodiment d a a..
a a **a Equation (46) is a theoretical equation which gives the power (Pwr) needed to move the block temperature to some desired value-without accounting for losses to the ambient 15 through the guardbands, etc.
Once the power needed to drive the block is determined via Equation this power is divided up into the power to be delivered to each of the three heater zones by the areas of these zones. Then the losses to the manifolds are 20 determined and a power term having a magnitude sufficient to compensate for these losses is added to the amount of power to be delivered to the manifold heater zone. Likewise, another power term sufficient to compensate for power lost to the block support pins, the block temperature sensor and 25 the ambient is added to the power to be delivered to the eddge heater zones. These additional terms and the division of power by the area of the zones convert Equation (46) to Equations and given above.
Equation (46) is the formula used by the preferred embodiment of the control system to determine the required 126 heating or cooling power to the sample block.
When the computed sample temperature is within the "integral band", 0.5°C around the target temperature the gain of the propr.'tional term is too small to close out the remaining error. Therefore an integral term is added to the proportional term to close out small errors.
The integral term is disabled outside the integral band to prevent a large error signal from accumulating. The algorithm inside the "integral band" is as follows: (47) Int_sum (new) Int_sum (old) (SP T (48) pwr_adj Ki Int_sum (new) where, Int_sum the sum of the sample period of the difference between the SP and 15 TsAXp temperature, and Ki the integral gain (512)- in the preferred embodiment).
Once a heating power has been calculated, the control software distributes the power to the three film heater zones 254, 262 and 256 in Figure 13 based on area_in-the 0,0 preferred embodiment. The edge heaters receive additional power based upon the difference between the block temperature and ambient temperature. Similarly, the 25 manifold heaters receive additional power based upon the difference between the block temperature and the coolant *0 gor 127 temperature.
PP Pseudocgd-e Upon System Power up or Reset Turn off ramp cooling .*10 Turn off all heaters Calculate heater resistances
*CS
Do Forever executes every 200ms If (block temperature 105) then Turn off heaters Turn on ramp valves Display error message Read the line voltage {linevolts} *0 Read the coolant sensor and convert to temperatur-e {h2otemp} Read the ambient sensor and convert to temperature S {Uambtamp} Read the heated cover sensor and convert to temperature {cvrtemp} Read the sample block sensor and oonvert to temperature (blktamp}. This portion of the code also reads the temperature stable voltage reference and compares the voltage to a reference voltage that was determined during calibration of the instrument. If there is any discrepancy, the electronics have drifted and the voltage readings from the temperature sensors are adjusted accordingly to obtain 128 accurate temperature readings.
Compute the sample temperature {tubetenths} or the temperature that gets displayed by using a low-pass digital filter.
(49) tubetenths TTn,. (TB, TTn,.) T/tau where last sample temp {tubetenths}
TB
n current block sensor temp {blktenths} T sample interval in seconds 200ms tau tau tube {cf_tau} tau sensor *10 {cflag} Equation (49) represents the first terms of a Taylor series expansion of the exponential that defines the o calculated sample temperature given as Equation above.
Compute the temperature of the foam backing underneath the sample block, {phantenths} known as the phantom mass. The temperature of the phantom mass is used to adjust the power delivered to the block to account for heat flow in and out of the phantom mass. The temperature is computed by using a low pass digital filter implemented in software.
(50) phantenths TT.n- (TB n TTn.) T/tau where TTn Last phantom mass temp {phantenths}
TB
n Current block sensor temp {blktenths} T Sample interval in seconds 200ms tauf Tau of foam block 30 secs.
Compute the sample temperature error (the difference between the sample temperature and the setpoint 129 temperature) {abstube_err}.
Determine ramp direction {fastramp} UP_RAMP or DN RAMP If (sample temperature is within ERR of setpoint
(SP))
then PID not in fast transition mode. {fastramp}
OFF
where ERR the temperature width of the "integral band", the error band surrounding the target or setpoint temperature.
10 Calculate current control cooling power {cool_ctrl} to determine how much heat is being lost to the bias cooling channels.
Calculate current ramp cooling power {cool_ramp} Calculate {cool_brkpt}. {cool_brkpt} is a cooling power that is used to determine when to make a .oo. transition from ramp to control cooling on downward ramps. It is a function of 0 block and coolant temperature.
o The control cooling power {cool ctrl} and the ramp cooling power {cool_ramp} are all factors which the CPU must know to control downward temperature ramps, to calculate how long to keep the ramp cooling solenoid operated valves open.
The control cooling power is equal to a constant plus the temperature of the coolant times the thermal conductance from the block to the bias cooling channels. Likewise, the ramp cooling power is equal to the difference between the block temperature and the coolant temperature times the thermal 130 conductance from the block to the ramp cooling Channels.
The- Cooling breakpoint is equal to a constant times the difference in tezperature between the block and the coolant.
S Calculate a heating or cooling power {intpwr needed to move the block temperature from its current temperature to the desired sQtpont (SP) temperature.
(51) {intpwr) XP CP C((8 T) {cfjkd) Tr, T ZL) 10 where; KP Proportional gain P/T in Equation es..
(46) approximately one in the preferred embodiment 0 0 CP Thermal mass of block .06:.15 SP Temperature setpoint T SAMP Sample temperature TRLK Block temperature cf )d Tau X Delta t where tau is the same tau as used in Equation (49) and Kd is 0 constant and Delta t is the 200 msec sample period.
If (sample temperature is within {cf-iband) of 0 &etpoint) then integrate sample error {i sum) else (52) clear (i_Ui
O.
Calculate the integral term power.
(53) integral trm J {i-sum} constant (cf_term).
Add the integral term to the power.
(54) f{int_pw'r) intpwr) integral term Adjust power to comp nsate for heating load due to the effects of the phantom inass (foam backing) by first 131 finding the phantom mass power then adding it to power {int pwr}.
(55) Calculate phantom mass power {phantpwr} by: phant_pwr C (blktenths phantenths) where: C thermal mass of foam backing (1.0 W/K) *0 0 000 0 0 0* 0, *0 *000 0 #0 Adjust heater power {intpwr} {int_pwr} {phant_pwr} Compute power needed in manifold heaters {auxl_power} which will compensate for loss from the sample block into the manifold edges that have coolant flowing through it.
Note that if the system is in a downward ramp, {auxl_power} 0. The manifold zone power required is described below: &o 0 0 0 00* e 00 0 0 0: 0 0 0 0.
*5 5
S
(57) {auxl_pcwer} K*(TBL TM)
K
2
*(TBL
K5*(dT/dt) where: K1 Coefficient {cf_lcoeff} K2 Coefficient {cf_2coeff} 20 K5 Coefficient dT/dt Ramp rate TsLK Block temperature Ty Ambient temperature TCO Coolant temperature -ITCOOL) Compute power needed in edge heaters {aux2_power} which will compensate for losses from the edges of the sample block to ambient. Note that if we are in a downward ramp {aux2_power} 0. The edge zone power required is described below: 132 10 *9*
S
.r S. S S.r
S..
(58) {aux2 K6*(dT/dt) where: K3 K4 K6
TILK
Tp
TCL
-CO1L _power} K 3
*(TIL
Coefficient {cf_3coeff} Coefficient {cf_4coeff} Coefficient {cf_6coeff} dT/dt Ramp rate Block temperature Ambient temperature Coolant temperature TAX) K4*(T IL T=L) Delete contribution of manifold {auxl_power} and edge heater power {aux2 power} to obtain total power that must be supplied by main heaters and coolers.
(59) {int_pwr} {int_power} {auxl_power} {aux2_power}
S
*5
S.
S
*5 S *5 5 a 5@ *0 S Decide if the ramp cooling should be applied. Note that {cool_brkpt} is used as a breakpoint from-ramp cooling to control cooling.
20 If (int_pwr cool_brkpt and performing downward ramp) to decide whether block temperature is so much higher than the setpoint temperature that ramp cooling is needed then Turn ON ramp valves else Turn OFF ramp valves and depend upon bias cooling At this point, {intpwr} contains the total heater power and {auxl_power} and {aux2_power} contain the loss from the block out to the edges. The power supplied to the auxiliary heaters is composed of two components: aux power and int_power. The power is distributed {intpwr} to the main and auxiliary heaters based on area.
total_pwr int pwr 133 intpwr total_pwr 66% auxl_power total_pwr 20% auxlpower aux2_power total_pwr 14% aux2_power Compute the number of half cycles for the triac to conduct for each end zone and each iteration of the control loop to send the appropriate amount of power to the heaters. This loop executes once every 1/5 second, therefore there are 120/5 24 half cycles at 60Hz or 100/5 20 at 50Hz. The number of half cycles is a function of requested power 10 {int_pwr}, the current line voltage {linevolts} and the heater resistance. Since the exact power needed may not be delivered each loop, a remainder is calculated {delta_power} to keep track of what to include from the last loop.
(60) intpwr int_pwr deltapower Calculate the number of 1/2 cycles to keep the triac on.
Index is equal to the number of cycles to keep the triac on.
(61) index power main heater ohms [20 or 24] linevolts squared where Equation (61) is performed once-for o: each heater zone and where "power" int pwr for the main heater zone, auxl_pwr for the manifold heater zone and aux2_pwr for the edge heater zone.
Calculate the amount of actual power delivered.
(62) actual_power linevolts squared index main heater resistance Calculate the remainder to be added next time.
(63) delta_power int_pwr actualpower 134 Calculate the number of 1/2 cycles for the edge and manifold heaters using the same technique described for the main heaters by substituting {auxlpwr} and {aux2pwr} into Equation Load the calculated counts into the counters that control the main, manifold and edge triacs.
Look at heated cover sensor. If heated cover is less than 100 0 C, then load heated cover counter to supply 50 watts of power.
10 Look at sample temperature. If it is greater than 50 0
C,
turn on HOT LED to warn user not to touch block.
END OF FOREVER LOOP
S
*S
135 Keyboard Task O The purpose of the keyboard task is to wait for the user to press a key on the keypad, compare the key to a list of valid keystrokes for the current state, execute the command function associated with the valid key and change to a new state. Invalid keystrokes are indicated with a beep and then ignored. This task is the heart of the state driven user interface. it is "state driven" because the action taken depends on the current state of the user interface.
Keyboard Task pseudocode: Initialize keyboard task variables.
Turn off the cursor.
0I0. If (install flag not set) then o* Run the install program.
15 Send a message to pid task to turn on the heated cover.
If (the power failed while the user was running a program) then Compute and display the number of minutes the power was off for.
Write a power failure status record to the history file.
a* Send a message to the sequence task to start a 4 0 C soak.
Give the user the option of reviewing the history file.
If (the user request to review the history file) then Go to the history file display.
25 Display the top level screen.
Do Forever Send a message to the system that this task is waiting for a hardware interrupt from the keypad.
Go to sleep until this interrupt is received.
When awakened, read and decode the key from the keypad.
Get a list of the valid keys for the current state.
Compare the key to the list of valid keys.
If (the key is valid for this state) then Get the "action" and next state information for this 136 key.
state. Execute the "action" (a co~and function) for this Go to the next state.
Else Beep the beeper for an invalid key.
End of Forever Loop 0 0 0 00 0 0600 0000 0 *000
S.
S..
6e 0* 6 5* 0 0S
S*
@0 S 0* B 0 S 00
S
@05000 *00* 0 0 Oe S 137 Timer Task Overview The purpose of the timer task is to wake up the sequence and the real time display task every half a second. The timer task asks the system (CRETIN) to wake it up whenever the half second hardware interrupt that is generated by the clock/calendar device is received. The timer task then in turn sends 2 wake up messages to the sequence task and the real time display task respectively. This intermediate task is necessary since CRETIN will only service one task per interrupt and thus only the higher priority task (the sequence task) would execute.
S S Timer Task Pseudocode: Do Forever Send a message to the system that this task is waiting for 15 a hardware interrupt from the clock/calendar device.
Go to sleep until this interrupt is received.
When awakened, send a message to the sequence and to the real time display-task.
End Forever Loop go oo 138 Sequence Task Overview The purpose of the sequence task is to execute the contents of a user defined program. It sequentially steps through each setpoint in a cycle, consisting of a ramp and a hold segment, and sends out setpoint temperature messages to the pid task which in turn controls the temperature of the sample block. At the end of each segment, it sends a message to the real time display task to switch the display and a message to the printer task to print the segment's runtime information. The user can pause a running program by pressing the PAUSE key on the keypad then resume the program by pressing the START key. The user can prematurely abort a program by pressing the STOP key. This task executes every half a second when it is awakened by the 15 timer task.
Sequence Task Pseudocode: Do Forever Initialize sequence task variables.
Wait for a message from the keyboard task that the user has 20 pressed the START key or selected START from the menu or a message from link task that the next program in a method is ready to run.
Go to sleep until this message is received.
When awakened, update the ADC calibration readings to account for any drift in the analog circuitry.
If (not starting the 4 0 C power failure soak sequence) then Send a message to the printer task to print the PE title line, system time and date, program configuration parameters, the program type and its number.
If (starting a HOLD program) then Get the temperature to hold at {hold_tp).
Get the number of seconds to hold for {hold_time}.
If (ramping down more than 3 0 C and {holdtp} 45 0 C) then 139 Post an intermediate setpoint.
O Else Post the final setpoint {hold_tp}.
While (counting down the hold time {hold_time}) Wait for half second wake up message from timer task.
Check block sensor for open or short.
If (keyboard task detected a PAUSE key) then Post a setpoint of current sample temp.
Send a message to wake up the pause task.
Go to sleep until awakened by the pause task.
Post pre-pause setpoint.
If (an intermediate setpoint was posted) then Post the final setpoint.
S 9. If (the setpoint temp is below ambient temp and will 15 be there for more than 4 min.) then Set a flag to tell pid task to turn off the heated cover.
Increment the half second hold time counter {store_time}.
Post the final setpoint again in case the hold time expired before the intermediate setpoint was reached this insures the correct setpoint will be written the history file.
"25 Write a data record to the history file.
Send a message to the printer task to print the HOLD info.
End of HOLD program Else if (starting a CYCLE program) then Add up the total number of seconds in a cycle {secs_in_run}, taking into account the instrument ramp time and the user programmed ramp and hold times.
Get the total number of seconds in the program by multiplying the number of seconds in a cycle by the number 140 of cycles in a program {num_cyc}.
Total {secs_in_run} {secs_inrun} per cycle {num cyc}.
While (counting down the number of cycles {numcyc}) While (counting down the number of setpoints {numseg}) Get the ramp time {ramp_time}.
Get the final setpoint temp {t_final}.
Get the hold time {local_time}.
Send a message to the real time display task to display the ramp segment information.
If (the user programmed a ramp time) then Compute the error {ramp err} between the programmed ramp time and the actual ramp time as follows. This equation is based on empirical 15 data.
{ramp_err} prog ramp_rate 15 0.5 (up ramp) g {ramp_err} prog ramp_rate 6 1.0 (down ramp) where:
S.
0 prog ramp_rate (abs(T, Tc) 1) {ramp_time) S S T, setpoint temp {t_final}
T
c current block temp {blktemp} abs absolute value of -the expression Note: the 1' is there because the clock starts within 10C of setpoint.
new ramp_time old {ramp_time} {ramp_err} If (new ramp_time old {ramp_time)) then new ramp_time old {ramp_time}.
Else 141 new ramp_time 0.
While (sample temp is not within a user configured temp {cf_clk_dev} of setpoint) Wait for half second wake up message from timer task.
Post a new ramp setpoint every second.
Else if (ramping down more than 30C and {t_final} 45°C) then Post an intermediate setpoint.
While (sample temp is not within a user configured Stemp {cfclkdev} of setpoint) 15 Wait for half second wake up message from timer task.
Increment the half second ramp time counter.
Check block sensor for open or short.
If (keyboard task detected a PAUSE key) then Post a setpoint of current sample temp.
Send a message to wake up the pause :5 task.
Go to sleep until awakened by -the pause task.
Post pre-pause setpoint.
Post the final setpoint.
While (sample temp is not within a user configured temp {cf_clk_dev} of setpoint) Wait for half second wake up message from timer task.
Increment the half second ramp time counter.
Check block sensor for open or short.
142 If (keyboard task detected a PAUSE key) then Post a setpoint of current sample temp.
Send a message to wake up the pause task.
Go to sleep until awakened by the pause task.
Post pre-pause setpoint.
Send a message to the printer task to print the ramp information.
Beep beeper to signal end of ramp segment.
Send a message to the real time display task to display the ramp segment information.
While (counting down the hold time) Wait for half second wake up message from timer task.
Increment the half second hold time counter.
Check block sensor for open or short.
~If (keyboard task detected a PAUSE key) then Post a setpoint of current sample temp.
Send a message to wake up the pause task.
Go to sleep until awakened by the pause task.
Post pre-pause setpoint.
Write a data record to the history file.
Send a message to the printer task to print the 5 hold information.
If (the final setpoint temp has drifted more than the user configurable amount {cf temp_dev}) then Write an error record to the history file.
Check for a programmed pause.
Go to next segment.
Send a message to the printer task to print an end of cycle message.
Go to next cycle.
End of CYCLE program.
143 Else if (starting an AUTO-CYCLE program) then Add up the total number of seconds in each program {secs_in run} taking into account the instrument ramp time and the user programmed hold times which can be automatically incremented or decremented by a programmed amount each cycle.
While (counting down the number of cycles {nun cyc}) While (counting down the number of setpoints {num seg}) Get the final setpoint temp {t_final}.
Get the hold time {time_hold}.
SCheck if the user programmed an auto increment or S"decrement of the setpoint temp and/or the hold time and adjust them accordingly.
15 If (the auto increment or decrement of the temp causes the setpoint to go below 0oC or above 99.9 0 C) then An error record is written to the history file.
The setpoint is capped at either 0oC or 99.9C.
Send a--message to real time display task to display the ramp segment information.
If (ramping down more than 3 0 C and {t final} 25 then Post an intermediate setpoint.
While (sample temp is not within a user configured temp {cf_clk_dev} of setpoint) Wait for half second wake up message from timer task.
Increment the half second ramp time counter.
Check block sensor for open or short.
If (keyboard task detected a PAUSE key) then 144 Post a setpoint of current sample temp.
Send a message to wake up the pause task.
Go to sleep until awakened by the pause task.
Post pre-pause setpoint.
Post the final setpoint.
While (sample temp is not within a user configured temp {cf_clk_dev} of setpoint) Wait for half second wake up message from timer task.
"Increment the half second ramp time counter.
15 Check block sensor for open or short.
S" If (keyboard task detected a PAUSE key) then Post a setpoint of current sample temp.
S Send a message to wake up the pause task.
Go to sleep until awakened by the pause task.
Post pre-pause setpoint.
Send a message to the printer task to print the ramp segment information.
Beep beeper to signal end of ramp portion of 5 segment.
Send a message to the real time display task- to display the hold segment information.
While (counting down the hold time) Wait for half second wake up message from timer task.
Increment the half second hold time counter.
Check block sensor for open or short.
If (keyboard task detected a PAUSE key) then Post a setpoint of current sample temp.
Send a message to wake up the pause task.
Go to sleep until awakened by the pause 145 task.
D Post pre-pause setpoint.
Write a data record to the history file.
Send a message to the printer task to print the hold information.
If (the final setpoint temp has drifted more than the user configurable amount {cftemp_dev}) then Write an error record to the history file.
Go to next segment.
Send a message to the printer task to print an end of cycle message.
Go to next cycle.
End of AUTO-CYCLE program.
15 Else if (starting a POWER FAILURE sequence) then o Post a setpoint of S" Set a flag {subamb_hold} so that the pid task will shut off the heated cover.
S DO FOREVER Wait for a half second wake up message from the timer task.
Increment the half second hold time counter.
END FOREVER
LOOP
End of power failure sequence Write a run end status record to the history file.
If (running a method) Set a flag {weird_flag} so the link task will know to send a message to the sequence task to start the next program running.
Else Return user interface to idle state display.
End of Forever Loop 146 Pause Task Overview The purpose of the pause task is to handle either a pause that the user programs in a CYCLE program or a pause when the user presses the PAUSE key on the keypad.
When the sequence task encounters a programmed pause while executing a CYCLE program, it goes to sleep and awakens the pause task. The pause task in turn sends a message to the real time display task to continually display and decrement the time the user asked to pause for. When the pause timer 10 times out, the pause task sends a message to awaken the o* sequence task and then goes to sleep. The user can prematurely resume the program by pressing the START key on the keypad or can prematurely abort the program by pressing the STOP key.
15 When the keyboard task detects a PAUSE key while a program is running, it sets a flag {pause_flag} then waits for the sequence task to acknowledge it. When the sequence task sees this flag set, it sends an acknowledgment message back to the keyboard task then puts itself to sleep. When the keyboard task receives this message, it awakens-the pause task. The pause task sends a message to the real time display task to continually display and increment the amount of time the program is paused for. The timer will time out when it reaches the pause time limit set by the user in the 25 configuration section. The user can resume the program by pressing the START key on the keypad or abort the program-by pressing the STOP key.
Pause Task Pseudocode: Do Forever Wait for a message from the keyboard task indicating a keypad pause, or a message form the sequence task indicating a user programmed pause.
Go to sleep until a message is received.
When awakened, check a flag for the type of pause initiated.
147 If (it is a programmed pause) then Send a message to the real time display task to display the pause timer counting up.
Else Send a message to the real time display task to display the pause timer counting down.
While (counting down the time out counter) Send a message to the system to suspend this task for half a second.
10 Send a message to the printer task to print the pause information.
If (it is a programmed pause) then The pause has timed out so send a message to the wake up the sequence task.
15 Send a message to the real time display task to halt the pause display.
Send a message to the real time display task to resume the running program display.
Else (it is a keypad pause) The pause has timed out and the program must be aborted so send a message to the system to halt the sequence task and send it back to the top of its FOREVER loop.
If (the program running was a HOLD program) Send a message to the printer task to print the hold information.
Write a status record to the history file.
Return the user interface to its idle state.
Display an abort message.
End of Forever Loop 148 Display Task Overview The purpose of the real time display task is to display temperatures, timers, sensor readings, ADC channel readings, and other parameters that need to be continually updated every half second.
Display Task Pseudocode: Initialize display task variables.
0 *0 Do Forever Wait for a message every half second from the timer task.
Go to sleep until the message is received.
When awakened, check if another task has sent a list of parameters to display or a flag to halt the current update.
Toggle the half second flag {half_sec}.
If (there's a list of parameters to display) then Set a semaphore so no one else will update the display.
Turn off the cursor. While (stepping through the list of parameters) *.20 If (it is a time parameter) then Display the time.
If (half second flag {half_sec} is set) then Increment or decrement the time variable.
Else if (it is a decimal number) then Display a decimal number.
Else if (it is an integer number) then Display the integer.
Else if (it is an ADC channel readout) then Read the counts from the ADC channel.
If (need it displayed as mV) then Convert counts to mV.
Display the value.
Else if (it is a power display) then Display the power in terms of watts.
149 Else if (it is the hours left parameter) then Convert seconds to tenths of hours.
Display the hours left in tenths of hours.
If (half second flag {half sec} is set) then Decrement the seconds variable.
If (the cursor was on) then Turn it back on.
Store the current system time in battery RAM.
Clear the semaphore to release the display.
*.10 End of Forever Loop g 0
S.
S.
S S e
S
oo S• 150 W Printer Task Overview The purpose of the printer task is to handle the runtime printing. It is a low priority task and should not interfere with other time critical tasks.
Printer Task Pseudocode: Do Forever Wait for a message from another task that wishes to print.
Go to sleep until a message is received.
When awaken, make local copies of the global variables to be printed.
Post a printer acknowledgement message.
If (need to print a status or error message) then Print the information contained in the current history record.
Else if (need to print the page header) then Print the company name, instrument ID, firmware version number and the current system time and date.
Else if (need to-print-the program header) then Print the type of program and its number.
20 Else if (need to print the program configuration parameters) then Print the tube type, reaction volume and the sample temperature deviation from setpoint that starts the clock.
Else if (need to print end of cycle information) then Print the ending time and temperature.
Else if (need to print segment information) then Print either the ramp or hold segment information.
Else if (need to print a pause status message) then Print the amount of time paused for and at what temp.
End of Forever Loop LED Task Overview The purpose of the LED task is to make the illumination of 151 the "Heating" LED reflect the power applied to the main heater. This is a low priority task that runs once a second.
LED Task Pseudocode: Initialize LED task variables.
Do Forever Send a message to the system to wake this task every second.
S Go to sleep.
O: When awaken, load counter 2 of PIC timer A with a value that reflects the power applied to the main heater as follows: load counter with value {K_htled) {htled} Where: 15- {K_htled} holds a constant to compute the time to pulse the heating LED and is equal to 15200 500.
15200 is a little greater than the PIC's clock of 14.4KHz and this is the value loaded into the timer to keep the LED constantly on. 500 is the main '0 heater power.
{ht led} will be a value between 0 and 500 and will be equal to the watts applied to the main heater.
End of Forever Loop Link Task Overview The purpose of the link task is to simulate the user pressing the START key on the keypad. This task is necessary so that programs can be executed one right after the other (as in a method) without user intervention. The link task wakes up the sequence task and it begins running 152 the next program as if the START key were pressed.
Link Task Pseudocode: Initialize link task variables.
Do Forever If (the flag {weird-flag} is set and it is not the first file in :the method) then Send a message to the sequence task to wake up.
End of Forever Loop 153 Start Up Sequence POWER-UP SEQUENCE When the power to the instrument is turned on or the software does a RESET, the following sequence takes place.
Note: the numbers below correspond to numbers on the flow chart.
1. Transmit a Ctrl-G (decimal 7) character out the RS- ^232 printer port. Poll the RS-232 port for at least 1 second and if a Ctrl-G is received, it is assumed 10 that an external computer is attached to the port and all communication during the power-up sequence will be redirected from the keypad to the RS-232 port. If no Ctrl-G is received, the power-up sequence continues as normal.
*.15 2. Check if the MORE key is depressed. If so, go straight to the service-only hardware diagnostics.
The next 3 tests are an audio/visual check and cannot report an error: 1) the beeper beeps 2) the hot, cooling, and heating LEDs on the keypad are flashed 3) each pixel of the display is highlighted. The copyright and instrument ID screens are displayed as the power-up diagnostics execute.
4. Should an error occur in one of the power-up diagnostics, the name of the component that failed is displayed and the keypad is locked except for the code 'MORE 999' which will gain access to the service-only hardware diagnostics.
Check channel 0 of the PPI-B device to see if the automated test bit is pulled low. If it is, run the UART test. If the test passes, beep the beeper continuously.
6. Start the CRETIN operating system which in turn will start up each task by priority level.
154 7. Check a flag in battery RAM to see if the instrument has been calibrated. If not, display an error message and lock the keypad except for the code 'MORE 999' which will gain access to the service-only calibration tests.
8. Run a test that measures the voltage and line frequency and see if both these values match the configuration plug selected while calibrating the instrument. If not, display an error message and .10 lock the keypad except for the code 'MORE 999' which will gain access to the service-only calibration tests.
9. Perform the heater ping test as described in the .go. Install section. If the heaters are wired wrong, display an error message and lock the keypad except for the code 'MORE 999' which will gain access to the service-only calibration tests.
*0 10. Check a flag in battery RAM to see if the instrument has been installed. If not, display an error message 2 0 and lock the keypad except for the code 'MORE 999' which will gain access to the install routine.
11. If not in remote mode, check a flag in battery RAM to see if there was a power failure while the instrument was running. If so, start a 4°C soak and display the amount of time the power was off for. Ask the user if they wish to view the history file which will tell them exactly how far along they were in the run when the power went off. If they select yes, they go straight to the user diagnostics.
12. Beep the beeper and clear the remote mode flag so all communication now is back through the keypad.
13. Check a flag in battery RAM to see if manufacturing wants their test program automatically started. If so, start the program running and reset the instrument after its done.
14. Display the top level user interface screen.
155 Referring to Figure 50, there is shown a crosssectional view of a larger volume, thin walled reaction tube marketed under the trademark MAXIAMP. This tube is useful for PCR reactions wherein reagents or other materials need to be added to the reaction mixture which will bring the total volume to greater than 200 microliters. The larger tube shown in Figure 50 made of Himont PD701 polypropylene or Valtec HH-444 polypropylene and has a thin wall in contact with the sample block. Whatever material is 10 selected should be compatible with the DNA and other o components of the PCR reaction mixture so as to not impair PCR reaction processing such as by having the target
DNA
stick to the walls and not replicate. Glass is generally not a good choice because DNA has been known to stick to the walls of glass tubes.
The dimension A in Figure 50 is typically 0.012 .001 inches and the wall angle relative to the longitudinal axis of the tube is typically 170. The advantage of a 17° wall angle is that while downward force causes good thermal t" '20 contact with the sample block, the- tubes do not ja-m in the sample wells. The advantage of the thin walls is that it S" minimizes the delay between changes in temperature of the 00440 sample block and corresponding changes in temperature of the reaction mixture. This means that if the user wants the ;25 reaction mixture to remain within 10C of 940C for 5 seconds in the denaturation segment, and programs in these parameters, he or she gets the 5 second denaturation interval with less time lag than with conventional tubes with thicker walls. This performance characteristic of being able to program a short soak interval such as a second denaturation soak and get a soak at the programmed temperature for the exact programmed time is enabled by use of a calculated sample temperature to control the timer. In the system described herein, the timer to time an incubation or soak interval is not started until the calculated sample temperature reaches the programmed soak temperature.
156 Further, with the thin walled sample tubes, it only takes about one-half to two-thirds as long for the sample mixture to get within l0C of the target temperature as with pri or art thick-walled microcentrifuge tubes and this is true both with the tall HAXIAMPU1 tube shown in Figure 50 and the smaller thin walled MICROA(P1 tube shown in Figure The wall thickness of both the HAXIAMP* and MICROAMP* tubes'is controlled tightly in the manufacturing process to be as thin as possible consistent with adequate structural strength. Typically, for polypropylene, this will be anywhere from 0.009 to 0.012 inches. If new, more exotic materials which are stroger than polypropylene are used to 00 achieve the advantage of speeding up the PCR reaction, the thickness can be less so long as adequate strength is 1maintained to withstand the downward force to assure good thermal contact, and other stresses of normal use. With a height (dimension B in Figure 50) of 1.12 inches and a 9' dimension C of 0.780 inches and an upper section wall 4 00 thickness (dimension of D) 0.395 inches, the MAXIAMP tube's 04 *020i-time constant is approximately 14 seconds although this has not been precisely measured as of the time of filing. The 0 MICROAMP tube time constant for the shorter tube shown in Figure 15 is tpclyapproximately 9.5 seconds with a tube wall thickness in the conical section of 0.009 inches plus 2 or minus 0.001 inches.
Figure 51 shows the results of use of the thinner walled MICROAMa' tube. A similar speeded up attainment of target temperatures will result from use of the thin walled MAXIAMP tube.
Referring to Figure 51, there is shown a graph of the relative times for the calculated sample temperature in a MICROAMP tube versus the time for a prior art tube to reach a temperature within 16C of a target denaturation temperature of 940C from a starting temperature of 72 0 C. in Figure 51, a 100 microliter sample was present in each tube.
The curve with data points marked by open boxes is the 157 calculated sample temperature response for a MICROAMP tube with a 9.5 second response time and a 0.009 inch wall thickness. The curve with data points marked by X's represents the calculated sample temperature for a 100 microliter sample in a prior art, thick walled microcentrifuge tube with a 0.030 inch wall thickness. This graph shows that the thin walled MICROAMP tube sample reaches a calculated temperature within 1oC of the 94.C target soak temperature within approximately 36 seconds 10 while the prior art tubes take about 73 seconds. This is important because in instruments which do not start their timers until the soak temperature is substantially achieved S the prior art tubes can substantially increase overall processing time especially when considered in light of the fact that each PCR cycle will have at least two ramps and soaks and there are generally very many cycles performed.
Doubling the ramp time for each ramp by using prior art tubes can therefore drastically increase processing time.
S: In systems which start their times based upon 20 block/bath/oven temperature without regard to actual sample S temperature, these long delays between changes in a block/bath/oven temperature and corresponding changes in sample mixture temperature can have serious negative consequences. The problem is that the long delay can cut into the time that the reaction mixture is actually at the temperature programmed for a soak. For very short soaks as are popular in the latest PCR processes, the reaction mixture may never actually reach the programmed soak temperature before the heating/cooling system starts attempting to change the reaction mixture temperature.
Figure 50 shows a polypropylene cap 650 connected to the MAXIAMP sample tube by a plastic web 652. The outside diameter E of the cap and the inside diameter F of the tube upper section are sized for an interference fit of between 0.002 and 0.005 inches. The inside surface 654 of the tube should be free of flash, nicks and scratches so that a gas- 158 tight seal with the cap can be formed.
Figure 52 shows a plan view of the tube 651, the cap 650 and the web 652. A shoulder 656 prevents the cap from being pushed too far down into the tube and allows sufficient projection of the cap above the top edge of the sample tube for making contact with the heated platen. This also allows sufficient cap deformation such that the minimum acceptable force F in Figure 15 can be applied by .c deformation of the cap.
*0 In the preferred embodiment, the tube and cap are 0000 made of Himont PD701 polypropylene which is autoclavable at temperatures up to 126 0 C for times up to 15 minutes. This allows the disposable tubes to be sterilized before use.
.0 Since the caps are permanently deformed in use in machines :15 with heated platens, the tubes are designed for use only once.
Caps for the MICROAMP tubes are available in connected strips of 8 or 12 caps with each cap numbered or as individual caps. Single rows of caps may be used and the 0:o 20 rows may be easily shortened to as few as desired or individual caps may be cut off the strip. Caps for MAXIAMP S. tubes are either attached as shown in Figure 50, or are S separate individual caps.
The maximum volume for post-PCR reagent additions to S..e 25 permit mixing on the MICROAMP tube is 200 microliters and is up to 500 microliters for the MAXIAMP tube. Temperature limits are -70 0 C to 126 0
C.
The response time depends upon the volume of the sample. Response is measured as the time for the sample to come within 37% of the new temperature when the block suddenly changes temperature. Typical response time for a microliter fill are 7.0 seconds and for a 20 microliter fill are 5.0 seconds.
159 APPENDIX A User Interface The objective of the GeneAmp PCR System 9600 user interface is to provide a simple way to develop and run programs that perform
PCR.
There are 3 types of programs available. The HOLD program consists of a single setpoint held for a set amount of time or held for an infinite amount of time and terminated by the STOP key. The CYCLE program adds the features of timed ramps and programmable pauses. This program allows up to 9 setpoints and up to 99 cycles. The AUTO program allows the user to increment or decrement the setpoint time and/or temperature a fixed amount every cycle. This program also allows up to 9 setpoints and.up to 99 cycles. A METHOD program provides a way to link up to 17 hold, cycle or auto programs together.
A total of 150 programs can be stored with numbers ranging from 1 to 150. Programs can be created, stored, protected, printed, or deleted. A directory of the stored programs can 20 be viewed or printed.
*:see* o 5 o •*ooo 160 THE SYSTEM 9600 KEYPAD g U
OE
WE
BAKSEg Heatin Cool in Hot
PAUS
*3 25 RPTIN 00 0@ 40 0 CE
SNTE
PAUSE OPTION23 EWE E
ENTER
starts a program running from the program display or restarts a programmed or keypad pause.
toggles the runtime displays and also accesses the service-only functions (if followed by the code 999).
moves to the previous field within the same screen. If currently positioned on the first field, it moves to the previous screen.
moves down to the first field in the next screen.
starts a paused time-out for manual interruptions.
either moves the cursor left-to-right through the menu items (rolling over to the leftmost option) or toggles the YES/No response.
aborts a running program or moves the user up one level in the user interface.
clears invalid numeric entries.
accepts the current numeric entry, accepts a menu item, accepts a YES/NO response, or skips to the next field of a display. If the numeric entry is the last of a display, ENTER steps to the next display.
161 COMMON SYSTEM 9600 DISPLAYS PROGRAM display __Example: Prog III Msg Temp Menu Prog is either HOLD, CYCL, AU i# is the program I(-5 stored yet Msg is either Done, Error,
A]
Temp is the current sample tei Menu are the available options RUNTIME display
M
S. S 0 S
SO.
*0eO So..
*05@
S..
15
S
S. 0@ 0 0 q S S OS S 00 S S ~A 5@.0@ 0 0@S*
S
S. S Action Temp Timer ?roq/Cc CYCL 117 Done 74.Oc.
R-STORE-PRINT-HOME
ro or METH 0) or if it is not bort or blank nperature 'Example: Ramp to 94.0C '29.6C 10:00 Cycle 14 'Ramp to xx.xC' ~perature time or counts up a hold -s @yce x1- counts up Example: Setpt 13 Tot Cyc Hrs left 2.5 Proq 17 Action is either 'Hold at xx.xC, 02 Temp is the current sample ter Timer counts down the hold or ramp time of
FOREVER
Prog/Cyc for a HOLD file is 'Prog for a CYCL or AUTO file MORE display Setpt -Tot Cyc Timer Progf Setpt is the current setpoint 1 counts up Tot Cyc is the total I of cycles (1-99) in the current program Timer is the time left in the program in hrs -counts down Prog is the current program 1 (1-150) KEYPAD PAUSE display Prog III Tep PAUSE Timer Tm I AamIp.Le: AUTO 118 PAUSE 9: 4 5 .5.
Prog is either HOLD, CYCL, AUTO or METH is the program 1 (1-150) or if it is not stored yet Temp is the current sample temperature 162 Timer is the configurable pause time counts down 0@ 0 0 0
S.
0 0e@0
OS@@
060 0000
SS
S. S S 0* 0S@* S. 0 SS S S S 0@ *0e0..
0 0000 S 0 S 0@ S 163 TOP LEVEL USER INTERFACE Select Option 9600
RUN-CREATE-EDIT-UTIL
I AT-EI-TI TOP LEVEL display Run SEnter program #xxx RUN display -1 Create program
HOLD-CYCL-AUTO-METH
CREATE display Edit Enter program #xxx Select function gIR-CONFIG-DIAG-DEL n EDIT display
~PIR-CONFIG~DIAG~DEL
UTIL display .o 10 15 00 o* 0 0S Programs are created by selecting a program type in the CREATE display. The user is brought directly to the first display of the program to be edited.
Stored programs are retrieved by entering a number 1 to 150 from the RUN, EDIT, or program displays. Entering a valid program number from the RUN display automatically begins the run. Entering a valid program number from the EDIT or program display brings the user to the first display of the program to be edited.
Programs are edited by pressing STEP (move down a screen), BACK (move to the previous field) or ENTER (move to the next field).
Programs are run by selecting RUN the EUN-STORE-PRINT-HOME menu or by pressing the RUN key on the keypad. The user must first enter 2 parameters required for each run.
:25 Tube type: MICRO React vol: 100uL The OPTION key toggles the tube type from MICRO (MicroAmp tube) to THIN (thin-walled GeneAmp tube). If the user configured a special tube, then the option of OTHER is added. A different reaction volume may be entered.
These parameters are stored with this program. ENTER accepts these values.
If the user configured the runtime printer ON and he is running a cycle, auto or method program, then the following Select print mode
OFF-CYCLE-SETPOINT
164 Q printer choices are offered. the program is started. CYCLE prints a message only upon completion of a cycle. SETPOINT prints runtime data for every setpoint (ramp/hold time and temps).
0 0 165 Select print mode
OFF-ON
Cover temp is xx*C Run starts at 100C If the user configured the runtime printer ON and he is running a hold program, then the following printer choices are offered.
If the heated cover is below 100°C, the following screen is displayed. If the user is on this display when the heated cover reaches 1006C, the run automatically begins. If the user hit STOP to return to the program display, then the run must be manually re-started.
Accepting HOME at the RUN-STORE-PRINT-HOME menu without saving a program displays the screen: 0 a a
S**
g000 a a. a.
9 a* OeaO a a 9* 0
S
Prog #xxx not stored Continue? YES -166 BOLD PROGRAM HOLD Ixxx xx.xc .UN-STORE-PRflq'p...ME PROGRAM display Hold FOREVER-xxcx: xx Beep while Hold? No The user can choose between an infinite soak or a time limited hold.
The beeper second.
will sound once S. 9 a a 4 64 .9*m a at..
4 4.
a *44 ~a a. 0 £4 4. *4 £4 a a 0 *a a 4 6* a a.
0 a a HOLD PROGRAM Runtime Aisplays Hold at xx.xc xx.xC xxx-Xx Proq xx-
I
RUNTIME display None MORE display
ENM
None PROGRAMMED PAUSE HOLD I xx .Xx.xC PAUSE xx:xx KEYPAD PAUSE display HOLD PROGRAM Runtime printout PE Cetus GeneAmp PCR System 9600 Ver xx.x Nov 14, 1990 ~..oxx:xx am :Tube type:MICRO Reaction vol:100uL Start clock within x.xC of setpt HOLD program Oxxx HOLD Program: xx.xC xxx:xx or Actual: xx.xC xxx:xx HOLD Program: xx.xC FOREVER Actual: xx.xc xxx:xx HOLD program lxxx Run Complete Nov 14, 1990 xx:xX am 167 CYCLE PROGRAM -CYCL #xxx xx.xC
RUN-STORE-PRINT-HOME
PROGRAM display x Temperature PCR' Setpt #1 Ramp xx:xx Sxx.xC Hold xx:xx The default is 3.
determines the number setpoints in this program.
9 setpoints are allowed.
This of 1 to 5 *foe 15 C S, 00:0 r *e 0 Total cycles x x Pause durinq run? NO Pause after isetpt
-J
Beep while pause?YES The number of setpoints entered above determines how many setpoint edit displays will be offered. The user can enter a ramp and hold time for each setpoint. The hold timer will start when the sample temp gets within a user configurable temp of setpoint.
If the user does NOT want to pause, then the next 3 displays are skipped. 1 to 99 cycles are allowed.
Entering a 0 for setpoint number also means the user does
NOT
want to pause therefore the next 2 displays are skipped.
The cycle number is limited to the total number of cycles entered above.
The default pause time is set in the user configuration.
ae.
25 1st pause :at cycl xx Pause every xx cvcs *e a esoe .00 Pause time xx:xx 168 CYCLE PROGRAM Runtime displays Ramp to xx.xc xx,xc.. Setpt,#x 'Tot Cyc xx xxx: xx Cycle xx Ers left X. x Procrxxx RUNTIME display (ramp) MORE display Hold at xxxC x .xC xxx: xx Cycle xx RUNTIME display (hold) CYCL Oxxx XX. xC PAUSE xx:xxc 0@ I S I
SE
5555
I
0000 5555
I
0*5*
S.
q 0050
SI
*5 I S I 55 5500 *1' 00 I 0 I 04 0000 0 4 00 2 .Setpt *x xx. xC KEYPAD PAUSE display E.PROGRAMMED
PAUSE
CYCLE PROGRAM Runt ize printout PE Cetus GeneAmp PCR System 9600 Ver xx.x N ov 14, 1990 xx:xx am Tube type:MICRO i-e&ction vol:lO0uL Start clock within x.xC of setpt CYCL program #xxx Cycle fxx Setpt Ix RAMP Program: xx.xC xx:xx Actual: xx.xC 0 xx:xx HOLD Program: xx.xC xx:xx Actual: xx. xC xx:xx (up to 9 setpoiits) (up to 99 cycles) CYCL program fxxx Run Complete Nov 14, 1990 xx:xx am CYCL program txxx User Ab~orted Nov 14, 1990 xx:xx am (only 0 if aborted)
I.
169 AUTO PROGRAM AUTO #xxx xx.xC
RSN-TORE-PRINT..HO
PROGRAM display x Temperature
PCR
The default is 3.
determines the number setpoints in this program.
9 setpoints are allowed.
This of 1 to Setpt #1 xx.xc S. Hold for xx:xx 10 15 Setpt fi xx.xC Change time/tem
?YES
U
U
The number of setpoints entered above determines how many setpoint edit displays will be offered. No ramp time is offered thus the instrument ramps as fast as possible. The hold timer start when the sample temp gets within a user configurable temp of setpoint.
If the user wants to increment or decrement the time and/or temperature every cycle, then the following display is offered.
The OPTION key toggles the arrow up (increment every cycle) or down (decrement every cycle).
The max time allowed to decrement is limited to the setpoint hold time.
Up to 99 cycles are allowed.
0 *.5 000 0 0 00 xx.xc delta x.xC delta xx:xx Total cycles x 170 AUTO PROGRAM Runtize displays Hold at xx.xcC XX.-XC xxx:xx Cycle xx-- RUNTIME display AUTO lx xx PAUSE xx:xx KEYPAD PAUSE display *Setpt Ix :-Tot Cyc xx* rsleft X.X Procrxxx MORE display :None PROGRAMM(ED PAUSE 0@ S 0 0 0* 0000 0 0000 05 0000
S.
000 *005 0S 5* 0 0@ 0 @0 5 *5 S S 0 0@ 2*O @0000.
S
0050 0 0 0@ 0 AUTO PROGRAM Runtize printout PE Cetus GeneAmp PCR System 9600 Ver xx.x Nov 14, 1990 xx:xx am Tube type:HICRO Reaction vol:loouL Start clock within x.xc of setpt AUTO program fxxx Cycle 1xx Setpt Ix RAMP Program: xx.xC xx:xx Actual: xx.xC _xx: xx HOLD Program: xx.xC xx:xx Actual: xx~xC xx: xx (up to 9 setpoints) (up to 99 cycles) AUTO program lxxx Run Complete Nov 12, 1990 xx:xx am AUTO program lxxx User Aborted Nov 12, 1990 xx:xx am (only if aborted) 171 METHOD PROGRAM I(ETH j#xxx xx. xC RUN-STORE-PRINr..HOE PROGRAM display __j 0 00 a Link progs: UP to 17 programs canibe linked in a method. If the user tries to enter a non-existant program J, the message "Prog does not exist" is displayed. If the user tries to link another method, the message "Cannot link a method" is displayed.
METHOD PROGRAM Runtime displays The RUNTIME, MORE and PAUSE displays will be those of the program currently running. Two additional MORE displays are offered when the program running is linked in a method.
0@ 9 9 15 0 S *9 9 99 9 0 9 9*
S
S.
9 0 0 00 9 The number of the program currently running will flash.
METH 1xxx aaa-bbbccc-ddd-eee-fffgq.
ADDITIONAL MORE display hhh-iii-j jj kkk-1ll- Tnlm-nnn-ooo-pppEL=" METHOD PROGRAM Runtime printout PE Cetus GeneAmp PCR System 9600 Ver xx.x Nov 14, 1990 xx:xx am Tube type:MICRO Reaction vol:lO0uL Start clock within x.xC of setpt METHOD program #xxx preceeds all linked program data 172 METHOD program xxx Meth Complete follows all linked progra data 0@
SO
S.
0505 0 5000
S
0*0* 0
S..
S. S* S S *5 0 *5 a S S 50 S. a.
S S 0@ S 05 S
S.
S
555055
S
55 SO S 0 50 0 173 METHOD PROGRAM -Print Select option METHOD-PRGRAM
DATA
METHOD prints the header of each program linked in the method.
PROGRAM DATA prints the header and contents of each program linked in the method.
0@ 0 0 0
S
S
F-
174 STORING A PROGRAM When STORE is selected from the RUN-STORE-PRINT-HOME menu, the routine for storing a program is the same for a file as well as a method. Protecting a program insures the user that the program will not be overwritten or deleted without knowledge of the user number. Other users will be able to view, edit, run, and link the protected file in their methods but will not be able to alter the stored version.
C
15
C
Store Enter program #xxx Progxxx is protected Enter user #xxxx Progxxx is protected Wrong user number! Progxxx is linked in Methxxx Continue?YES Can't overwrite prog Linked in method xxx Store Protect program?
NO
Store Enter user #xxxx xxx is the first available program number from 1 150.
The user has entered the f of a protected program. The correct user must be entered in order to overwrite this program.
The wrong user was entered.
This display remains for seconds before reverting to the previous one. The user is given 3 chances to enter the correct i.
If the user tries program that is method, the user given the option or not.
to overwrite a linked in a is warned and of continuing 60 *0~25 00* 0 see*: 4 S 30 5015
S
C. 6 If the user tries to overwrite a program that is linked in a method with another method, an error message is given.
The user is given the chance to protect a program as well as unprotect a previously protected program.
The user wants to protect the program and therefore must enter a user Ready to store the program in an available slot. The user f appears only if the program is protected.
175 Prog Oxxx User #xxxx OK to store?
YES
Prog Ixxx User Ixxxx OX to overwrite?
YES
Ready t 0 overwr ite an existi nl g progra The user j appear s only if the progra m is protec ted. *6 0 S B 40 0
S
0000 *0 0 000 0004 S B. S p 04 0 176 UTILITY
FUNCTIONS
select function flIR-CONFIG-DIAG-.DEL UTIL display
DIR
allow the user to view or print a directory of the stored programs by either their program number, user number or program type.
CONPIG allows the user to tailor the use of the instrument to their specific needs.
DIAG of fers the user a means of diagnosing runtime problems and verifying the performance of the ins trument.
a. 0 S S S S.
sga~O
DEL
90* a *6 9.
S
*650 S S a 64 S
S*
05 S. .0 9 4 SS 0.
*eS 04.
5* -S 9 allows the user to delete stored programs by program number, user number or program type.
177 UTIL
DIRECTORY
Directo ry
PROG-TYPE-USER.-PRINT
Directory by PROGram niumber Enter proqram fxxx Programs will be listed in numerical order starting at the given number. The STEP and BACK keys move through the directory displays. The beeper sounds at the beginning or end of the program list.
STOP returns the user to the above display.
a. .ir~
S
C, 00 0gOe a 6 a 000'
S
~S0
S.
0I 0o S HOLD if124 Directory by program
TYPE
Direc tory
HOLD-CYCL-ATTO..H
The program numbers will be listed for the selected type of program.
BS
00 0 0@ 0000 00 6a a CYCL 115 se: Directory by USER niumber 0 Enter user 1xxxx METH 1150 User #1234 All programs stored under the given user number will be listed.
Directory
PRINT
178
I
Directory Prini PROG-TYPE-US
ER
The user can get a hardcopy of the directory listing in the same manner the directory is viewed above.
0 S.
0 0 0 0 179 UTIL USER CONFIGURATION Configuration
EDIT-PRINT
The configuration file can be edited by accepting EDIT from the menu or by pressing the STEP key. PRINT prints the contents of this file.
Time: xx:xx Date: mm/dd/w The user can set the system time and date.
Runtime printer OFf Runtime beeper
ON
C.
C..
SC..'15 *15 .o 2 Pause time-out limit xx:xx '*25 30 *o* Allowed setpt error x.xoC Idle state setpoint xx°C If the runtime printer is ON, the user will be prompted with printer option as the start of each run. If the runtime beeper is ON, then a beep will sound at the end of each segment (after a ramp or hold portion of a sequence) while running a program.
This time represents the maximum :amount of time a program can pause for before it is aborted.
This pertains only to the keypad 'pause. This time represents the number of degrees the actual sample temp may vary from the setpoint before an error is flagged.
This setpoint is useful for balancing the control cooling power which is always present.
The sample temp will be maintained at the idle state setpoint whenever the instrument is idle.
The clock which times the hold segment of a running program can be configured to be triggered when it gets within this temperature of the sample temp.
The nominal value is Start clock within x.xOC of setpoint If the user wishes to use a different type of tube other than the MicroAmp or Thin-walled GeneAmp tubes, they must set this option to YES and enter at least 3 pairs of 180 -M reaction volume and tube time Special tube? NO constant data. This curve will be used to extrapolate the correct Tau (tube time constant) for each run using this special tube depending on the reaction volume entered by the user at the start of a run.
0 0 00- 0..0 0: ,00:0.
181 UTIL USER CONFIGURATION (cont) Rxn Vol3xxicuL T-xxxs Rxn vol1xxjuL T=xxxs 3 sets of this screen will be offered if the user sets "Special tube?" to YES.
S
0 9 0S 0.*
S
S. 55 OSS S
S
505* 9
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0 0050 0 0 00 9 182 UTIL
DELETE
Delete
PROGRAM-USER-ALL
Delete by PROGRAM Delete Enter program #xxx All programs (files and methods) can be deleted by number.
Can't S Linked delete progxxx Sin methodxxx! A program cannot be deleted if it linked in a method.
S..
S. Progxxx is protected Enter user #xxxx Progxxx is protected Wrong user number! Prog #xxx User #xxxx Delete program? YES The user has entered the of a protected program. The correct user must be entered in order to delete this program.
The wrong user was entered.
This display remains for seconds before reverting to the previous one. The user is given 3 chances to enter the correct
I.
Ready to delete the program. The user appears only if the program was protected.
Delete by USER Delete Enter user fxxxx Delete SNo progs with #xxxx Programs can be deleted under a given user number.
If no programs exist with the given user the following message is displayed.
183 Progs linked in meth STEP to listpos Programs cannot be deleted if they are linked in a method. The STEP key will cycle through the list of linked programs.
S. S S S
S.
S..
S
5555 0O*O
S
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S
5555 S S 55
OS
S S *5@S
SS
S. S 05 S S S
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5555 S S OS 184 UTIL DELETE (cont) Can't delete progxxx Linked in zfethodx! User #xxxx Deeeall. prog s?YES The list of the linked programs will Show which method the program is linked to.
This will delete all the programs under the given User that are not linked.
Delete
ALL
Ce S C C we eC r~ 0*gg Cogs 0* g g.e gee.
C S Ce 0 eg
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eg egg.
Ce eg 0 Oe 0 0 S gO
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see e.g 0 gsee 5 C go C Delete every unprotected prog?YES This Will delete every unprotected program that is nt linked in a protected method.
185 UTIL USER DIAGNOSTICS While running any diagnostic test, the STOP key always returns the user to the top level diagnostic screen and automatically increments the test number and name to the next test. This facilitates manually cycling through the available diagnostics.
Enter Diag Test #f0 REVIEW HISTORY FILE
F
REVIEW HISTORY
FILE
The user can enter the number of the diagnostic to run or can use the STEP or BACK keys to cycle through the available tests.
Every time the STEP or BACK key is pressed, the test number is incremented or decremented and the associated test name is displayed. This feature eliminates the need for the user to memorize the number associated with each test.
.0 S .4 Enter Diag Test #f REVIEW HISTORY
FILE
25 C 05
C
*0 .me.
@0
S
The history file is a circular buffer in battery RAM which can store up to 500 records of the latest run. When the buffer is full, the oldest entries will be overwritten. The buffer will automatically be cleared before a program is executed.
The history file header displays the current number of records in the file S ALL views all the records STAT views only the status records ERRORS views only the records with error messages PRNT prints all or part of the history file HISTORY nnn recs
ALL-STAT-ERRORS-PRNT
r.
The two types of records are 1) status records which give information about the program and 2) data records which give information abount each hold and ramp segment in a program.
A Hold program is treated as one hold segment and the data record will be stored when the file ends.
Since there could be hundreds of entries (50 cycles X 6 setpoints 350 entries), fast, bi-directional movement through the file is required. Note that most PCR programs will be 3 or 6 setpoints and 40 cycles or less. The entries will normally be reviewed in reverse order, thus the first 186 record seen will be the last record written.
S If the user has chosen a type of record to view, STEP or BACK will move down or up the buffer by one entry of the chosen type. By preceding STEP or BACK with a number, the second line is replaced with "Skip #XXX entries". The user enters a number and presses ENTER to accept the value and that number of entries is skipped going forward (STEP) or backward
(BACK).
By preceding STEP or BACK with the RUN key, the user can quickly move to the largest record I (the newest record) or record #1 (the oldest record) of the chosen type.
STOPerterminates the review mode and displays the file header.
0 *o*
S
*O o e o g 187 STATUS RECORD
MORMON
'ffff #xxxfmmm .pssage .nnn
I
A
S
ffff' is either HOLD, CYCL or
UTO
xxx' is the program number /mmm' is the method number for linked program, else blank
S
S
'nnn' is the recor Status messages Tube Type: xxxxx Reaction vol: xxxuL Clk starts w/in x.xC Start xx/xx/xx Xx:xx End xx/xx/xx xx:xx Meth Complete Pause xx:xx at xx.xC 20 Fatal status messagei Sensor Error Power fail xxx.x hrs User Abort Pause Timeout xx:xx Fatal Setpoint Error .0 d number 'message' is one of the following: Type of sample tube used in the run Reaction volume used in the run The hold clock starts within this temp of setpoint Time and date of the start of the run Time and date of the end of the run All programs linked in the method are complete The program paused for this time at this temp i A sensor had a bad reading times in a row The power was off for this amount of time The user pressed the STOP key during the run The keypad pause has reached its configurable time limit.
Is the requirement to abort a program if the setpoint is not reached within a calculated amount of time. A 10 X 10 lookup table of starting ramp temperature (0oC 100 0 C in 100C increments) vs. ending ramp temperature (same axis labeling) will hold the average time the TC2 should take to ramp up or down any given amount of degrees. The file will be aborted if the setpoint is not reached in the amount of time calculated as follows: .t programmed ramp time (2 lookup table value) minutes DATA RECORD is either HOLD, CYCL or AUTO xxx' is the program number 188 ffxxx/mmm ddd.dC nnn Cycyy Setnt z nmm:ss '/nnm' is the method number for a linked program else blank Iddd.d' is the ending setpoint temp I n n n is the record number 'yy' is the cycle number 'zI is the setpoint number *'ifl*ss' is the setpoint time The cycle and setpoint number fields will be omitted for a Hold program.
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6 me
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S.
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189 DATA ERROR RECORD
I
'ddd.d' is the ending setDoint message ddd.dC nnn temp Cycyy Setpt z mmm:ss 'nnn' is the record number 'yy' is the cycle number is the setpoint number mmm:ss' is the setpoint time 'message' indicates a non-fatal error as follows: Non-fatal Error messages Setp Error The setpoint was not reached in the calculated time: .59 0* 20 *52 value).
Prog Error Temp Error programmed ramp time (2 lookup table An Auto program auto increment/decrement of the setpoint temp or time caused the hold time to go negative or the temp to go out of the range 0.10C to 100 0
C.
At the end of the segment, the setpoint temp has drifted a user configurable amount.
For the Hold program, the cycle and setpoint fields will be omitted.
04 b 9 9* 8 e e 190 PRINTING THE HISTORY
FILE
Access to the history file print routines is through the history file header menu. The OPTION key cycles the cursor through the options: HISTORY nnn recs
ALL-STAT-ERRORS-ERNT
Pressing the ENTER key when the cursor is positioned under PRNT displays the print screen: Print History
ALL-STAT-ERRORS
ALL prints all the records in the file STAT prints only the status records ERRORS prints only the records with error messages j When one of print options is selected, the following screen is displayed: Print History Print from prog #xx
S
The first (most recent) program number will be the default program. The user can change the program number from which to begin printing. While printing, the following screen is ":66j5 displayed: Print History printing At the end of printing, the Print History menu is again displayed.
191 HEATER TEST Enter Diag Test #2f HEATER TEST The heater test calculates the heat rate of the sample block as its temperature rises from 350C to 65 0 C. The following creen is displayed as it forces the block temperature to 350C.
Heater Test Blk=XX.X going to 0600 0 osee 1 00 0e When the temperature stabilizes, all heaters are turned on full power. The display now reads "going to 65C" and the block temperature is monitored for 20 seconds after it passes 50 0 C. After 20 seconds, a pass or fail message is displayed.
Heater Test PASSES a g *e 0 0J 0 192 CHILLER
TEST
Enter Diag Test .1i CHILLER TEST The chiller test calculates the cool rate of the sample block as its temperature drops from 350C to 150C. The following screen is displayed as it forces the block temperature to 35 0
C.
Chillr Test Blk-XX.X going to When the temperature stabilizes, the chiller is on. The .display now reads "going to 15C" and the block temperature is monitored for 20 seconds after it passes 250C. After seconds, a pass or fail message is displayed.
i0 g o Chiller test PASSES I S
S
S. S

Claims (9)

1. In a thermocycler apparatus suitable for performing a polymerase chain reaction, which thermocycler apparatus includes a metal sample block having an array of spaced-apart sample wells each of which has an inside surface, said wells being capable of receiving one or more capped sample tubes each containing a sample mixture placed in a microtiter plate having an uppermost edge, which plate is seated on said sample block, a cover to enclose said capped sample tubes, which cover comprises a flat, horizontal rectangular portion and downwardly projecting skirt portions along the periphery thereof and further comprises a device for heating at least the underside of said o0 horizontal portion, said cover being dimensioned to contact said sample block and to enclose said microtiter plate and capped sample tubes on said sample block and to apply heat and a downwardly directed force on said sample tubes.
2. The cover of claim 1 wherein said side portions are dimensioned such that is said skirt portions contact said sample block at substantially the same time as the undderside of said cover contacts the uppermost edge of said microtiter plate as the cover encloses the plate.
3. The cover of claim 2 wherein the downwardly directed force is sufficient to ensure a snug contact between a lower portion of each sample tube and the inside surface 20 of the well which contains said portion.
4. The cover of claim 1 further comprising knob and screw means for lowering said cover from one height to another, said knob and screw means including indication means for identifying a knob position corresponding to the cover height at which said cover contacts said uppermost edge. 25
5. The cover of claim 1 which provides sufficient heating to said capped sample tubes so as to heat the caps and the portions of the sample tubes positioned above the sample wells to a temperature above a condensation point of vapour from the sample mixture in said one or more tubes.
6. A cover as defined in claim 1, substantially as hereinbefore described with reference to the accompanying drawings.
7. In a thermocycler apparatus suitable for performing a polymerase chain reaction having a sample well which is capable of receiving at least one capped plastic sample tube containing a sample mixture, the improvement comprising a heated cover to RA aid in providing flush contact between said at least one sample tube and said sample well. I R:\LIB3A]04359doc:mrr 194
8. A thermocycler apparatus for performing a polymerase chain reaction, comprising a cover according to any one of claims 1 to 6.
9. In a thermocycler apparatus suitable for performing a polymerase chain reaction having a sample well which is capable of receiving at least one capped plastic sample tube containing a sample mixture, the improvement comprising a heated cover to aid in providing flush contact between said at least one sample tube and said sample well, substantially as hereinbefore described with reference to the accompanying drawings. Dated 18 October, 2001 Perkin-Elmer Cetus Instruments Patent Attorneys for the Applicant/Nominated Person SPRUSON FERGUSON S*6 66 *6 a o, So A [R:\LIBA04359doc:mrrr
AU97002/98A 1990-11-29 1998-12-09 Thermal cycler for automatic performance of the polymerase chain reaction with close temperature control Expired AU741806B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU97002/98A AU741806B2 (en) 1990-11-29 1998-12-09 Thermal cycler for automatic performance of the polymerase chain reaction with close temperature control

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US620606 1990-11-29
US670545 1991-03-14
AU24934/95A AU696482B2 (en) 1990-11-29 1995-07-11 Thermal cycler for automatic performance of the polymerase chain reaction with close temperature control
AU97002/98A AU741806B2 (en) 1990-11-29 1998-12-09 Thermal cycler for automatic performance of the polymerase chain reaction with close temperature control

Related Parent Applications (1)

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AU741806B2 true AU741806B2 (en) 2001-12-13

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Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989009437A1 (en) * 1988-03-26 1989-10-05 Peter Duncan Goodearl Dean Reaction temperature control

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989009437A1 (en) * 1988-03-26 1989-10-05 Peter Duncan Goodearl Dean Reaction temperature control

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