WO2016081892A1 - Systems and methods for identification and differentiation of viral infection - Google Patents
Systems and methods for identification and differentiation of viral infection Download PDFInfo
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- WO2016081892A1 WO2016081892A1 PCT/US2015/061970 US2015061970W WO2016081892A1 WO 2016081892 A1 WO2016081892 A1 WO 2016081892A1 US 2015061970 W US2015061970 W US 2015061970W WO 2016081892 A1 WO2016081892 A1 WO 2016081892A1
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/70—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving virus or bacteriophage
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- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6844—Nucleic acid amplification reactions
- C12Q1/686—Polymerase chain reaction [PCR]
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B25/00—ICT specially adapted for hybridisation; ICT specially adapted for gene or protein expression
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B25/00—ICT specially adapted for hybridisation; ICT specially adapted for gene or protein expression
- G16B25/20—Polymerase chain reaction [PCR]; Primer or probe design; Probe optimisation
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B30/00—ICT specially adapted for sequence analysis involving nucleotides or amino acids
- G16B30/10—Sequence alignment; Homology search
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16B—BIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
- G16B99/00—Subject matter not provided for in other groups of this subclass
Definitions
- the field of the invention is diagnostic systems and methods for rapid identification and differentiation of viral infections, especially as it relates to infection with Ebola virus and differentiation from a symptomatically similar Influenza virus infection.
- influenza A (“flu”) is believed to infect between 5-20% of the population annually resulting in about 200,000 hospital admissions and about 39,000 flu-related deaths.
- pandemic periods such as the most recent 2009-2010 "Swine Flu”
- these numbers have risen by an additional 43-89 million cases (resulting in between 8,870 to 18,300 additional estimated influenza related deaths).
- ebolaviruses also demonstrate pandemic potential and share early clinical symptomology with influenza A infection, including the presence of fever, muscle/body aches, headaches, and severe fatigue. Such similarity poses particular challenges where a flu epidemic coincides with presence or suspicion of Ebola infections.
- Rapid identification and differentiation of the viral pathogen is of utmost importance as clinical care and epidemiological containment of influenza patients (e.g., home care with antiviral drug) differs significantly from protocols required for Ebola patient care (e.g., largely dependent on quarantine with palliative support).
- Diagnosis of Ebola infection can be performed in numerous manners and uses viral nucleic acid detection methodologies in most cases. For example, detection of many filovirus species by reverse transcription-polymerase chain reaction using a primer set specific for the viral nucleoprotein gene has been reported to rapidly cover a large variety of virus species that include Ebola and Ebola-related viruses (/ Virol Methods. 2011 Jan; 171(l): 310-3). Such method advantageously allows quick analysis, but unfortunately fails to provide differential diagnostic value against other non-filoviruses. In another approach of viral diagnosis, total RNA from patient serum was subjected to PCR amplification followed by next generation sequencing (Virology 2012 Jan 5;422(1): 1-5).
- Greene SCPrimer is a software suite (see e.g., Nucleic Acid Res. 2006, Vol 34, No.22 p: 6605-6611) that generates in a first step a phylogenetic tree of all sequences for a virus family to identify candidate primers and then runs a greedy set covering problem (SCP) algorithm to so arrive at minimum primer sets that are then further pruned to match melting points for forward and reverse primers.
- SCP greedy set covering problem
- While facilitating selection of primer pairs, such analysis is computational complex and may still not cover all viruses in a viral family or species.
- such method still requires use of degenerate primers, which increases risk of non-specific binding. Still further, such methods also tend to become problematic where viral target sets are very diverse.
- MPP multiplex primer prediction
- primers for distinct classes of pathogens can be determined using consensus sequences from members of the distinct classes. Most typically, the consensus sequences are obtained by successive alignment and processing of the various pathogen sequences, correction for human sequences, and set difference operation between the respective primers for the distinct classes.
- the inventors contemplate a method of obtaining sets of primers for differentiation of two unspecified pathogens.
- each of the unspecified pathogens belong to distinct phylogenetic pathogen ⁇ e.g., virus) families, and each pathogen family comprises multiple distinct pathogen species and/or serotypes.
- contemplated methods include a step of performing respective multiple sequence alignments, via an alignment device, for a plurality of digitally represented genomes of the pathogen species and serotypes of the respective distinct pathogen families to produce an alignment output for each of the distinct pathogen families.
- Such methods will also include a step of identifying in each alignment output respective consensus sequences having (i) a homology above a minimum threshold, (ii) a length above a minimum threshold, and (iii) a melting temperature above a minimum threshold.
- identified consensus sequences are collected into respective adjusted alignment outputs for the distinct pathogen families, and in a still further step, sequences are eliminated from the respective adjusted alignment outputs sequences (the eliminated sequences will have a minimum homology to human and human-hosted sequences) to so form respective virus-specific alignment outputs.
- a set difference analysis is then performed on the virus-specific alignment outputs to so obtain respective sets of consensus sequences for the unspecified pathogens, and primer sequences are then selected from the respective sets of consensus sequences.
- the multiple sequence alignment is performed using Clustal X, Clustal W, or Clustal Omega. It is further contemplated that the minimum threshold for the homology is at least 97% (and in some cases the homology is 100%), the minimum threshold for the length is at least 15, and more typically at least 20, and most typically at least 25 bases, while the minimum threshold for the melting temperature is at least 60 °C, and more commonly at least 65 °C.
- an analysis engine is programmed/configured to process a formatted output from Clustal X, Clustal W, or Clustal Omega, containing alignments of several different members of a pathogen family or order (e.g., influenza A and influenza B). By comparing the alignment of nucleobases of every viral member, regions of conservations can be found. These regions of conservation are then collected for development of primer sequences to uniquely identify all members of a class of pathogens. In cases where regions of conservation are not found or that the regions fail to yield oligomers that meet the melting temperature requirements, this algorithm will allow minimal mismatch bases to reach the desired melting point.
- Each base position within the alignment is an assigned a conservation score such that upon addition of mismatch bases, the base position that are most representative of viral class will be used to allow the largest degree of compatibility.
- the primer sequences are then filtered using BlastN to remove any potential mapping to human sequences, reducing the false positive rate. Subsequent analysis the removes sequences that overlap. It is further generally preferred that the step of eliminating is performed using BlastN, wherein the minimum homology to human and human-hosted sequences (e.g., viral sequence known or suspected to be present in the human) is at least 90%, and more typically at least 95%.
- the set difference analysis is performed using Set Difference and Set Union operations, and/or that the primer sequences are selected to produce an amplicon has a length of between 100 and 800 bases. It is also contemplated that the unspecified pathogens belong to two distinct phylogenetic orders. Finally, it is contemplated that methods may further include a step of determining a primer sequence to produce a cDNA from a viral RNA, and/or that the set of primers comprises between one and five primer pairs for each of the unspecified pathogen.
- Figure 1 is an exemplary schematic flow diagram of a computer founded method of primer identification according to the inventive subject matter.
- the inventors have now discovered systems and methods for multiplexed differential detection of one or more strains of a pathogen (e.g., Ebola virus) against one or more strains of another pathogen (e.g., Influenza virus) in a single sample where it is not known a priori which of the pathogen(s) and/or strains are present.
- the detection is based on sets of oligonucleotides targeting various symptomatically similar viruses, and especially Ebola virus (Zaire) and influenza A in biological samples, which are most commonly whole blood or serum, or plasma.
- all of the oligonucleotides target highly conserved areas (in some cases 100% conserved across every strain), and have a melting point Tm > 65 °C.
- contemplated assay are not used to differentiate and identify a single serotype among a choice of many, but to distinguish between unknown (unspecified) classes of pathogens while covering most or all of the serotypes within each class.
- contemplated primers will also be selected such as to exclude non-target specific binding, and especially binding to the host genome or nucleic acids expected or known to be present in the host genome.
- primers are selected such that primer dimers and cross hybridization (i.e., primer designed for first class of pathogen binds to second class of pathogen) is avoided.
- the inventors used a conceptually simple and effective computer implemented algorithm to identify unique target sequences against which to design the primer panels (in either the complementary or reverse complementary orientation) to so enable rapid identification of influenza A and/or Ebola virus containing samples.
- contemplated systems and methods will be suitable for any pathogens as the inventive subject matter is independent of the specific sequence information.
- the systems and methods described herein are suitable to rapidly identify numerous target sites (and with that individual and multiplex possibilities), enabling an end user to select the best primer pair(s) for their particular amplification platform.
- Figure 1 exemplarily shows a typical computer implemented work flow according to the inventive subject matter.
- All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context.
- the use of any and all examples, or exemplary language (e.g. "such as") provided with respect to certain embodiments herein is intended merely to better illuminate the invention and does not pose a limitation on the scope of the invention otherwise claimed. No language in the specification should be construed as indicating any non-claimed element essential to the practice of the invention.
- a first step 1 all available nucleic acid sequences for a class of pathogens (e.g., all members of a pathogen genus or species serotypes) are obtained from one or more sources, typically from sequence databases in a digital FASTA format. There are many such databases known in the art, and all of the databases are deemed suitable for use herein.
- the data format need not necessarily be limited to FASTA format, and various alternative formats are also contemplated, including FASTQ, BAM, SAM, EMBL, GCG, GenBank, RAW, IG, etc.
- FASTA format is generally preferred and it should be recognized that other formats can be re-formatted to FASTA format where so desired.
- the databases may provide the data online or that the database may be a physical file on CD-ROM, EPROM memory, etc.
- the sequence data are preferably acquired by an analysis engine that is configured to allow for a rapid alignment of multiple sequences as shown in step 120.
- Most preferably such alignment is a multi-sequence alignment, and especially preferred aligners include those that use seeded guide trees and HMM profile-profile techniques to generate alignments, such as ClustalO, to produce a corresponding alignment in Clustal format 130.
- alignments may also be performed in numerous alternative manners and may use alignments based on local regions (e.g., Kalign), based on fast Fourier transforms (e.g. , MAFFT), or based on phylogeny- aware methods (e.g., WebPRANK).
- processing step 140 preferably uses the entire multi- sequence alignment in an approach where consensus sequences for the entire alignment are identified that have (i) a homology above a minimum threshold, (ii) a length above a minimum threshold, and (iii) a melting temperature above a minimum threshold.
- consensus sequences are incrementally identified for areas where the homology is at or above a predetermined threshold (e.g., at least 90%, at least 95%, at least 97%, at least 99%, or 100%) for a predetermined minimum or maximum length (typically between at least 15 bases, at least 20 bases, at least 25 bases, at least 30 bases, at least 40 bases, at least 50 bases, etc., and less than 100 bases, less than 90 bases, less than 70 bases, etc.).
- length determination will also be a function of a desired melting point. Most typically, the melting temperature is at least 60 °C, or at least 65 °C, or at least 68 °C. Therefore, in at least some aspects of the inventive subject matter, the consensus sequences so identified will have a minimum threshold for length of at least 20 bases, a minimum threshold for homology of at least 97%, and a minimum threshold for the melting temperature is at least 60 °C.
- predetermined homology it is contemplated that a user will provide the desired minimum threshold, and in most cases the minimum threshold will be above 90% homology.
- suitable minimum homology thresholds include 95%, 96%, 97%, 98%, 99%, and 100%.
- the degree of minimum homology will be a function of the diversity and number of class members for the pathogen, and it is generally preferred that the minimum threshold is lower (e.g., at least 95%) for a more diverse class whereas relatively conserved classes may have a higher minimum threshold (e.g., at least 98%).
- a user will provide the necessary minimum length and suitable minimum lengths will be at least at least 15 bases, at least 20 bases, at least 25 bases, at least 30 bases, at least 40 bases, at least 50 bases, etc.
- the actual length may be determined by the analysis engine using the minimum length, the required minimum homology, and the desired minimum melting temperature (for each of the sequences).
- the melting point determination can be carried out using Formula (I) for oligonucleotides with a size of less than 13 bases and according to Formula (II) for oligonucleotides that have a size of equal to or greater than 13 bases.
- Tm 64.9 +41 *(G+C-16.4)/(A+T+G+C) ( ⁇ )
- Primers are typically retained/selected in length such that the oligonucleotides meet or exceed a predetermined melting point (e.g. , 65 °C).
- a predetermined melting point e.g. , 65 °C.
- the so identified consensus sequences are then collected into respective adjusted alignment outputs for the distinct pathogen families. Viewed form a different perspective, each pathogen will have its own adjusted alignment output with all of the sequences matching the minimum thresholds for homology, length, and melting temperature.
- the predetermined melting temperatures for the first and second distinct pathogen classes are no more than 5 °C apart, more typically no more than 4 °C apart, even more typically no more than 3 °C apart, and most typically no more than 2 °C apart (e.g., same temperature).
- the analysis engine in step 140 takes in output files from Clustal X, Clustal W, or Clustal Omega, containing alignments of different pathogen species that typically belong to one pathogen order, family, or genus. Given these alignment files the analysis engine searches for regions of conservation across all members, preferentially identifying regions where the bases are 100% conserved. Failing to find regions that are 100% conserved, the analysis engine will report the highest conserved region. From these regions, the analysis engine will generate potential oligomers of varying sizes: suitable minimum lengths will be at least at least 15 bases, at least 20 bases, at least 25 bases, at least 30 bases, at least 40 bases, at least 50 bases, etc.
- step 160 the so identified and characterized consensus sequences in respective adjusted alignment outputs are then further processed in an analysis engine as shown in step 160 to remove sequences that would match in sequence (or hybridize under PCR conditions) human sequences and/or other sequences that can be reasonably expected to be at least potentially present in a human.
- Sequence matching can be done in a variety of manners, and all known manners are deemed suitable for use herein. However, particularly suitable matching algorithms include BlastN to identify matching sequences.
- any matching sequences e.g., sequences with homology of >70 , more typically >80 , and most typically >90 ; or Tm difference to human or other virus target of less than 7 °C, more typically less than 5 °C, and most typically less than 3 °C
- Tm difference to human or other virus target of less than 7 °C, more typically less than 5 °C, and most typically less than 3 °C
- further processing will help eliminate false positive assay results that may be due to binding of the primers to the host (e.g., human) genome.
- the inventors then perform a set difference analysis on the pathogen-specific alignment outputs 162 and 164 to so obtain respective sets of consensus sequences for the pathogens.
- the set difference analysis 170 is run as set difference and set union operations (typically using FASTA formatted files) that will then produce unique sequences 172 against both pathogen classes suitable for use as primers in diagnostic PCR reactions.
- the term 'Set' is a collection of nucleobases representing the sequences found in the previous steps
- the term 'set difference' is defined as the elements of one set, B that are not present in another set A. In the present instance, those differences would be oligomers.
- Set Union is defined as the elements of Set A that are also in Set B. Given these two operations, the Symmetric Set Difference yields all oligomers that do not overlap from Set A and Set B.
- the analysis engine in step 170 will treat each file as a set of oligomers that identify a pathogen family uniquely. Once these sets are created, set difference and set union operations are performed to discover oligomers that belong to multiple sets of pathogen families. These oligomers are then eliminated, as they are unable to uniquely identify one pathogen family from another. The rest of the oligomers are then returned as sets of oligomers that uniquely identify 1 viral family and can then be mixed with other oligomers that uniquely identify a separate pathogen family within the same assay (e.g., a DNA chip).
- sequences presented herein may be synthetic oligonucleotides and oligonucleotide analogs, and that all calculations of melting temperatures will consider the changes in temperature due to the different chemistries.
- the sequences may include a peptide nucleic acid backbone, a sugar-phosphate, or sugar phosphonate/sulfonate backbone.
- the bases in contemplated sequences may be the naturally occurring nucleobases (e.g., adenine, thymine, cytosine, guanine, uracil), but also non-naturally occurring bases making stable or unstable hydrogen bonds with naturally occurring bases (e.g., inosine, iso-C, iso-G, PICS, 3MN, 3FB, MICS, etc.).
- suitable oligonucleotides may have degenerate bases in one or more position, or have bases that allow for mismatch.
- all of the nucleobases will optionally include a radioisotope or other isotope (e.g. , NMR- active label).
- the backbone may include one or more labeled moieties.
- the oligonucleotide will be a single type of oligo, typically a DNA oligomer.
- RNA oligomers or mixed-type oligomers are also considered suitable for use herein.
- suitable oligomers include those that have a affinity marker (e.g., biotin) or other label for direct (e.g., fluorophore, radioisotope) or indirect identification and/or quantification.
- kits will include at least one pair of oligonucleotides suitable to produce an amplification or ligation product via a PCR or LCR reaction.
- pairs will be selected to be either specific to a particular strain or serotype of virus, or to cover multiple strains or serotypes.
- multiple pairs of oligonucleotides it is generally contemplated that such pairs will be selected to have minimal or no cross-reactivity between viral targets and/or amplification products, and that such pairs can be used concurrently in a multiplexed reaction.
- multiplexing PCR or LCR will especially be performed using pairs of oligos that will target specific sequences of different viruses (e.g., Ebola virus and InfluenzaA virus).
- oligonucleotides will target highly conserved regions of the viral genome (e.g., RNA-dependent RNA polymerase start structure) and have similar or even identical melting points. Therefore, the inventors contemplate a selection of oligonucleotides that can be employed in a custom assembled kit to readily identify selected viruses. Exemplary sequences and compositions are shown in more detail below.
- the above examples provides many example embodiments of the inventive subject matter. Although each embodiment represents a single combination of inventive elements, the inventive subject matter is considered to include all possible combinations of the disclosed elements. Thus if one embodiment comprises elements A, B, and C, and a second embodiment comprises elements B and D, then the inventive subject matter is also considered to include other remaining combinations of A, B, C, or D, even if not explicitly disclosed.
- any language directed to a computer should be read to include any suitable combination of computing devices, including servers, interfaces, systems, databases, agents, peers, engines, controllers, or other types of computing devices operating individually or collectively.
- the computing devices comprise a processor configured to execute software instructions stored on a tangible, non-transitory computer readable storage medium (e.g., hard drive, solid state drive, RAM, flash, ROM, etc.).
- the software instructions preferably configure the computing device to provide the roles, responsibilities, or other functionality as discussed below with respect to the disclosed apparatus.
- the disclosed technologies can be embodied as a computer program product that includes a non-transitory computer readable medium storing the software instructions that causes a processor to execute the disclosed steps associated with
- the various servers, systems, databases, or interfaces exchange data using standardized protocols or algorithms, possibly based on HTTP, HTTPS, AES, public -private key exchanges, web service APIs, known financial transaction protocols, or other electronic information exchanging methods.
- Data exchanges among devices can be conducted over a packet-switched network, the Internet, LAN, WAN, VPN, or other type of packet switched network; a circuit switched network; cell switched network; or other type of network.
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Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
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CN201580068630.5A CN107429302A (en) | 2014-11-21 | 2015-11-20 | System and method for the identification and differentiation of virus infection |
EP15860469.4A EP3221472A4 (en) | 2014-11-21 | 2015-11-20 | Systems and methods for identification and differentiation of viral infection |
JP2017527213A JP2017535270A (en) | 2014-11-21 | 2015-11-20 | System and method for identification and differentiation of viral infections |
US15/527,930 US20180258501A1 (en) | 2014-11-21 | 2015-11-20 | Systems And Methods For Identification And Differentiation Of Viral Infection |
CA2968527A CA2968527C (en) | 2014-11-21 | 2015-11-20 | Systems and methods for identification and differentiation of viral infection |
AU2015349661A AU2015349661B2 (en) | 2014-11-21 | 2015-11-20 | Systems and methods for identification and differentiation of viral infection |
KR1020177016784A KR20180008374A (en) | 2014-11-21 | 2015-11-20 | Systems and methods for identification and differentiation of viral infection |
IL252393A IL252393A0 (en) | 2014-11-21 | 2017-05-19 | Systems and methods for identification and differentiation of viral infection |
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US201462083125P | 2014-11-21 | 2014-11-21 | |
US62/083,125 | 2014-11-21 |
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WO2016081892A1 true WO2016081892A1 (en) | 2016-05-26 |
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PCT/US2015/061970 WO2016081892A1 (en) | 2014-11-21 | 2015-11-20 | Systems and methods for identification and differentiation of viral infection |
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US (1) | US20180258501A1 (en) |
EP (1) | EP3221472A4 (en) |
JP (2) | JP2017535270A (en) |
KR (1) | KR20180008374A (en) |
CN (1) | CN107429302A (en) |
AU (1) | AU2015349661B2 (en) |
CA (1) | CA2968527C (en) |
IL (1) | IL252393A0 (en) |
WO (1) | WO2016081892A1 (en) |
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US20060204996A1 (en) * | 2005-03-08 | 2006-09-14 | Kwon Tae-Joon | Method of designing primer and probe sets, primer and probe set designed by the method, kit comprising the sets, computer readable medium recorded thereon program to execute the method, and method of identifying target sequence using the sets |
US20070259337A1 (en) * | 2005-11-29 | 2007-11-08 | Intelligent Medical Devices, Inc. | Methods and systems for designing primers and probes |
US20090105092A1 (en) * | 2006-11-28 | 2009-04-23 | The Trustees Of Columbia University In The City Of New York | Viral database methods |
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GB0113907D0 (en) * | 2001-06-07 | 2001-08-01 | Univ London | Virus detection using degenerate PCR primers |
US8032310B2 (en) * | 2004-07-02 | 2011-10-04 | The United States Of America As Represented By The Secretary Of The Navy | Computer-implemented method, computer readable storage medium, and apparatus for identification of a biological sequence |
EP1895989A2 (en) * | 2005-06-03 | 2008-03-12 | Egalet A/S | A solid pharmaceutical composition with a first fraction of a dispersion medium and a second fraction of a matrix, the latter being at least partially first exposed to gastrointestinal fluids |
US9434997B2 (en) * | 2007-08-24 | 2016-09-06 | Lawrence Livermore National Security, Llc | Methods, compounds and systems for detecting a microorganism in a sample |
US20130267429A1 (en) * | 2009-12-21 | 2013-10-10 | Lawrence Livermore National Security, Llc | Biological sample target classification, detection and selection methods, and related arrays and oligonucleotide probes |
US20110152109A1 (en) * | 2009-12-21 | 2011-06-23 | Gardner Shea N | Biological sample target classification, detection and selection methods, and related arrays and oligonucleotide probes |
CA2833912C (en) * | 2010-04-23 | 2021-09-21 | University Of Massachusetts | Aav-based treatment of cholesterol-related disorders |
JP5936829B2 (en) * | 2011-07-11 | 2016-06-22 | 東洋製罐グループホールディングス株式会社 | Primer preparation method, primer usage method, primer set, PCR reaction solution, and primer design method |
CN103646193B (en) * | 2013-12-24 | 2016-07-06 | 辽宁大学 | A kind of PCR primer method for designing differentiated for nearly edge species |
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2015
- 2015-11-20 EP EP15860469.4A patent/EP3221472A4/en not_active Withdrawn
- 2015-11-20 WO PCT/US2015/061970 patent/WO2016081892A1/en active Application Filing
- 2015-11-20 CN CN201580068630.5A patent/CN107429302A/en not_active Withdrawn
- 2015-11-20 AU AU2015349661A patent/AU2015349661B2/en active Active
- 2015-11-20 JP JP2017527213A patent/JP2017535270A/en active Pending
- 2015-11-20 KR KR1020177016784A patent/KR20180008374A/en not_active Application Discontinuation
- 2015-11-20 US US15/527,930 patent/US20180258501A1/en not_active Abandoned
- 2015-11-20 CA CA2968527A patent/CA2968527C/en active Active
-
2017
- 2017-05-19 IL IL252393A patent/IL252393A0/en unknown
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US20060204996A1 (en) * | 2005-03-08 | 2006-09-14 | Kwon Tae-Joon | Method of designing primer and probe sets, primer and probe set designed by the method, kit comprising the sets, computer readable medium recorded thereon program to execute the method, and method of identifying target sequence using the sets |
US20070259337A1 (en) * | 2005-11-29 | 2007-11-08 | Intelligent Medical Devices, Inc. | Methods and systems for designing primers and probes |
US20090105092A1 (en) * | 2006-11-28 | 2009-04-23 | The Trustees Of Columbia University In The City Of New York | Viral database methods |
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Also Published As
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US20180258501A1 (en) | 2018-09-13 |
AU2015349661A1 (en) | 2017-06-15 |
CA2968527C (en) | 2019-01-29 |
IL252393A0 (en) | 2017-07-31 |
EP3221472A4 (en) | 2017-11-22 |
CA2968527A1 (en) | 2016-05-26 |
AU2015349661B2 (en) | 2019-05-16 |
JP2017535270A (en) | 2017-11-30 |
JP2019058175A (en) | 2019-04-18 |
EP3221472A1 (en) | 2017-09-27 |
CN107429302A (en) | 2017-12-01 |
KR20180008374A (en) | 2018-01-24 |
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