CN110554039B - Laboratory microorganism detection system for realizing laboratory microorganism detection method - Google Patents

Laboratory microorganism detection system for realizing laboratory microorganism detection method Download PDF

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CN110554039B
CN110554039B CN201910772352.1A CN201910772352A CN110554039B CN 110554039 B CN110554039 B CN 110554039B CN 201910772352 A CN201910772352 A CN 201910772352A CN 110554039 B CN110554039 B CN 110554039B
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迟海鹏
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Beijing Dynaflow Experiment Technology Co Ltd
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Abstract

The invention belongs to the technical field of laboratory detection equipment, and particularly relates to a laboratory microorganism detection system which can realize a laboratory microorganism detection method with more comprehensive detection and higher accuracy, which specifically comprises the following steps: a color table construction module; a spectrum scanning module matrix; a refractive index difference comparison module; an image noise reduction module; and the microbial color table is compared with a confirmation module. The microorganism detection system or the detection method provided by the invention has the advantages that the color contrast data of the conventional environment is constructed as the basis, the detection image is obtained through polarized light scanning, and the abnormity of the laboratory environment is detected through the accurate denoising and contrast method, so that the system has higher precision, wider scanning range and more comprehensive detection.

Description

Laboratory microorganism detection system for realizing laboratory microorganism detection method
Technical Field
The invention belongs to the technical field of laboratory detection equipment, and particularly relates to a laboratory microorganism detection system for realizing a laboratory microorganism detection method.
Background
In the 40's of the 20 th century, the united states established a biological weapons research program and began to implement an "aerosol infection program" that utilized large numbers of pathogens as highly contagious diseases and continued to develop a series of microbiological, weaponry, and field tests. However, due to insufficient protection technology and consciousness of the microbiological experiment at that time, workers are not protected in place during the experiment, so that the infection accidents in the laboratory operation frequently occur. In 1979, anthrax bacillus leakage accidents occurred in anthrax drying plants in weapons research base in the Soviet-Victorloff region during production, which caused inhalation anthrax or skin anthrax to infect a large number of residents downwind of the base, and led to the death of dozens of people. Along with the research of high-risk pathogens, laboratory biosafety accidents continue to continue in this period, developed countries such as English, American, Soviet Union, Canada, Japan and the like successively start the construction of biosafety laboratories to solve the safety problems, and the frequency of the laboratory biosafety accidents is reduced through the operation of different levels of biosafety laboratories and corresponding microorganism operation standard guidelines.
In 1979, the American Occupational Safety and Health Agency (OSHA) issued a pathogenic microorganism classification based on degree of harm, and first proposed the concept of four grades of pathogenic microorganisms and experimental activities thereof. In 1983, in order to reduce the occurrence of laboratory safety accidents, the WHO published the first version of the laboratory biological safety manual, and continuously revised the manual to guide various countries to carry out standardized management on the biological laboratories of the country, and made specific operating rules to guide the safe operation of pathogenic microorganisms. In 2004, after absorbing the laboratory management experience and the safety accident experience training of each country, the newly revised handbook (third edition) made clear requirements for hardware and software including facilities and equipment, personal protection and SOP in the laboratory. Meanwhile, in order to realize safer laboratory management and biosafety control, biological safety laws and regulations of the country are successively set up by each country, laboratory safety supervision and inspection are enhanced, and infection and leakage of pathogenic pathogens in the laboratory are controlled.
In the 80 s of the 20 th century, epidemic hemorrhagic fever laboratory infection accidents occur continuously in the world, and a three-level biosafety level (BSL-3) laboratory made in the first country of China is built by military medical academy of sciences for safely carrying out the experimental research, and relevant operation regulations are made. Subsequently, in order to develop AIDS research, a few BSL-3 laboratories were introduced by the original Chinese academy of preventive medicine, and the construction of the BSL-3 laboratories in China began. Meanwhile, the national biological safety standard is prepared from the end of the last 90 th century in China, and the national standard of biological safety of laboratories in China, namely the universal requirement of biological safety of laboratories (GB19489), is promulgated in 5 2004. On the basis, various departments issue respective laboratory biological safety regulations and rules successively to guide biological safety guarantee of microbial laboratories in various fields.
With the continuous establishment of BSL-3 laboratories and the successive promulgation of relevant standard laws and regulations, the safety of high-risk pathogen experimental work in China is basically guaranteed, but in practical application, the occurrence of biological safety accidents can still be caused by pathogen exposure caused by instrument equipment failure or human accidental factors, for example, in 2004, a certain laboratory researcher in Beijing uses an unverified inactivation method to treat a SARS-CoV sample, then the sample is carried out of the BSL-3 laboratory, and then the experiment is carried out in a common laboratory, so that active viruses are carried out and cause the infection of the laboratory, and then close contacts are infected, and finally 9 people are infected, and 1 person dies. The BSL-3 laboratory ensures the safety of experimental activities, but becomes a risk factor of biological safety, and needs a practitioner to carry out more detailed work, discover the specific risk factor of the laboratory, make scientific and effective control measures and avoid the occurrence of laboratory accidents.
How to invent a laboratory microorganism detection system which can achieve more comprehensive and higher accuracy inside a laboratory by integrally detecting the microorganism environment inside the laboratory and effectively detecting and reducing noise simultaneously becomes an urgent task for solving the problems in the biochemical laboratory at present.
Disclosure of Invention
The invention aims to provide a laboratory microorganism detection system which is more comprehensive in detection and higher in accuracy.
The invention also aims to provide a laboratory microorganism detection method.
The purpose of the invention is realized as follows:
a laboratory microorganism detection system specifically comprises:
the building module is used for building a color table to be confirmed according to the spectral data characteristics of the laboratory;
the system comprises a scanning module, a data acquisition module and a data processing module, wherein the scanning module is used for carrying out optical scanning on the whole environment of a laboratory to obtain a corresponding environment scanning result and converting the environment scanning result into corresponding spectrum data;
the comparison module is used for acquiring the refractive index of a scanning position related to the overall environment of the laboratory scanned by light according to the spectral data acquired by the scanning module; searching and comparing the refractive index difference of each scanning position based on a prestored refractive index mapping table;
the image denoising module is used for denoising the image file to be scanned;
and the confirming module is used for searching a color value which is closest to the refractive index difference of each scanning position searched and compared by the comparison module based on the color table to be confirmed, which is constructed by the construction module, determining the index color corresponding to the image file to be scanned after the noise reduction processing is carried out by the image noise reduction module, and obtaining the microorganism scanning result.
(1) Pre-constructing a color table according to the spectral data characteristics of a laboratory, comprising:
(1.1) constructing a spectral data set Q:
Q={Q1,Q2,Q3,…Qi…,Qn}
Qnobtaining the spectrum data for the nth time, wherein n is the total times of obtaining the spectrum data;
(1.2) acquiring a value of the spectral data at each time;
Qn=(Q1,n,Q2,n,Q3,n,…Qj,n,…,Qm,n)
Qm,nthe characteristic value is the mth spectral characteristic value when the spectral data is acquired at the nth time, and m is the total characteristic value quantity when the spectral data is acquired each time;
(1.3) carrying out standardization treatment;
Figure GDA0003288551810000021
Zm,nfor the purpose of the normalized value of the value,
Figure GDA0003288551810000022
for the mean, σ Q, of the n-th acquired spectral datanA variance for the nth acquired spectral data;
(1.4) constructing a confirmation color table;
Figure GDA0003288551810000031
Bmfor the mth spectral feature value of the constructed color chart, Q _1mIs the maximum of all the mth spectral characteristic values in the spectral data set Q;
(2) converting environmental scan results into spectral data, comprising the steps of:
the whole environment of the laboratory is optically scanned to obtain a series of polarized light, the light is reflected when entering a detection interface of the laboratory, and the reflected light is as follows:
Figure GDA0003288551810000032
Figure GDA0003288551810000037
is the included angle between the incident light of the polarized light and the S-polarization; ksAnd KpPredetermined coefficients of S-polarization and P-polarization, respectively, and KsAnd KpThe following conditions are satisfied;
Figure GDA0003288551810000033
k1 is the reflectance of polarized light in a laboratory environment; k2 is the reflection coefficient of the polarized light with the mycoderm, beta is the polarization coefficient of the polarized light, and beta is obtained by the following formula;
Figure GDA0003288551810000034
lambda is the refractive index of the detection surface;
the spectral data of the emergent light is:
Figure GDA0003288551810000035
θithe included angle between the polarized light and the normal vector is shown, and F _ C is spectrum data of emergent light;
(3) converting the refractive index of the scanned position according to the spectral data; mapping index is carried out on the data of each position, the refractive index of each position is used for mapping with a refractive index comparison table, the comparison table is compared, and the refractive index difference is detected;
the imaging system outputs an image of the object as:
Figure GDA0003288551810000036
c is the imaging system channel number; f. ofc(x) For the C-th channel in the imaging systemThe xth position of the track outputs a response value; rc(mu) is the spectral integrated response curve of the C channel; sigmac(μ) is the response curve of the light source spectrum of the C-th channel; dc(mu) spectral power curve of light source of C channel, Pc(μ) is the spectral transmittance curve of the pre-channel filter for the C-th channel, μ is the integrated parameter, with no practical meaning, x is the imaging system output object image position, C is 1, 2, 3 … … q, q is the total number of channels;
the output images of all channels are represented in a discrete matrix manner:
Figure GDA0003288551810000041
f (x) is the output image of all channels,
Figure GDA0003288551810000042
the spectral reflectance of the light-scanned image surface;
r (mu) is a diagonal matrix formed by the spectral comprehensive response curves of all channels;
Figure GDA0003288551810000043
σ (μ) is a diagonal matrix formed by response curves of the light source spectra of all channels;
Figure GDA0003288551810000044
d (mu) is a diagonal matrix formed by spectral power curves of light sources of all channels
Figure GDA0003288551810000045
P (mu) is a diagonal matrix formed by the spectral transmittance curves of the channel front filters of all channels;
Figure GDA0003288551810000046
calculating the mapping relation between the light scanning image and the color table through the inverse transformation of the positive image model of the spectral imaging system;
(5) denoising the scanned image file; comprises the following steps of;
(4.1) acquiring a scanned image file W;
(4.2) dividing the scanned image W into N blocks, the image W being N partial images, i.e., W ═ W1,W2,W3,…,Wi,…,WNAnd arbitrary local image WNAll satisfy the following formula;
WN=CSN+LBN
CSNpixel matrix, LB, of the original image of the Nth partial imageNA filtered pixel matrix for an nth image;
(4.3) solving for said WNThe singular characteristic quantity WV of the pixel ofNAnd said WNVariance σ ofN
(4.4) calculating an energy function of the local image;
Figure GDA0003288551810000051
wherein, fCSNIs the energy function of the local image, | WN-CSN||FIs WN-CSNF-norm, | | CSN||w*Is a weighted norm and meets the following requirements;
Figure GDA0003288551810000052
wherein j belongs to m and is a value of j, and m is a singular characteristic quantity WVNThe number of values contained, d is the sum of the local image WNThe Euclidean distance of less than 0.1, K is a preset value, | SVN|jThe original singular value is obtained by the following formula;
Figure GDA0003288551810000053
wherein, | WVN|jIs WVNThe jth value of (d);
(4.5) obtaining LB by the energy function of the partial imageN
Figure GDA0003288551810000054
The CS can be obtained by constructing an equation system by using the formulas in (4.5) and (4.2)NI.e. to the local part WNRemoving the filtered image, and removing the filtering of all the N local images to obtain the image from which the filtering is removed;
the pre-constructing of the color table according to the spectral data characteristics of the laboratory comprises:
(1.1) extracting a color table of the image in the first clustering:
Q1={z1、z2、…zn};
zncollecting color points of a laboratory environment image, wherein n is the number of the color points;
(1.2) clustering for the second time to obtain an extended color table;
Figure GDA0003288551810000061
wherein σ is a spreading factor; and the secondary clustering refines the color table in the block. The association of colors and the diversity of color combinations within a block are maintained.
(1.3) carrying out standardization treatment;
Figure GDA0003288551810000062
zij *is a normalized value, zijTo expandColor point values in the color table; alpha is the mean value of all sample data; β is the standard deviation of all sample data;
(1.4) carrying out brightness self-adaptation;
Figure GDA0003288551810000063
Itlis the mean value of brightness, Ct, of the color chartlIs the original brightness value, Pt, of the color chartlIs the mean value of the brightness, Im, of the color chartlAs the mean value of the brightness, Cm, of the imagelIs the original brightness value, Pm, of the imagelIs the contrast luminance mean of the image.
Scanning the whole environment of laboratory is a series of polarized light, and the reflection takes place when light incides laboratory detection interface, and the reverberation is:
Figure GDA0003288551810000064
Figure GDA0003288551810000065
the included angle between the polarization direction of the polarizer and the S polarization component is formed; r issAnd rpPolarization coefficients for the S and P polarization components, respectively;
Figure GDA0003288551810000066
r01the polarization reflection coefficients of the laboratory environment and air; r is12The polarization reflection coefficients of the laboratory environment and the bacteria-carrying membrane are obtained;
delta is the polarized light phase difference;
Figure GDA0003288551810000067
niis the refractive index of the detection surface; thetaiAn incident angle of the detection light for the detection plane;
the spectral data of the emergent light is:
Figure GDA0003288551810000068
Figure GDA0003288551810000069
is the angle between the polarized light and the long axis.
Converting the refractive index of the scanned position according to the spectral data; mapping and indexing the data of each position, mapping the refractive index of each position and a refractive index comparison table, comparing the comparison table, and detecting the refractive index difference, including;
the imaging system outputs an image of the object as:
ck=∫λrk(λ)ρk(λ)sk(λ)o(λ)dλ;
k is the imaging system channel number; c. CkIs the output response of the k channel in the imaging system; r (λ) is the spectral response curve; s (lambda) is a response curve of the light source spectrum; o (λ) is the spectral power spectrum of the light source, ρk(λ) the spectral transmittance of the front filter of each channel;
expressed in a discrete matrix manner as:
Cn=(Rnρn)TSnRn;
dn is a multi-channel image output by the imaging system; sn is the spectral reflectivity of the surface of the optical scanning image; is a diagonal matrix with diagonal elements r (λ); the elements on the diagonal are the spectral responsivity of the imaging system at each wavelength;
Figure GDA0003288551810000071
tn is the spectral transmittance of the imaging system;
Figure GDA0003288551810000072
sn is a diagonal matrix taking the spectral power distribution of the light source as diagonal elements;
Figure GDA0003288551810000073
cn is an erect image model of the spectral imaging system;
and calculating the mapping relation between the light scanning image and the color table through the inverse transformation of the positive image model of the spectral imaging system.
Denoising the scanned image file; comprises the following steps of;
(4.1) all image information documents g (t) { g ═ g1,g2,g3,…,gNConstructed as an m × n-order document matrix, giThe ith image information document being the font, image information document set g (t);
(4.2) setting the dimension n of the document matrix;
(4.3) extracting { g ] from G (t)1,g2,g3,…,gnAs the first row of the matrix;
(4.4) sequentially delaying backward by one document until the last signal of n lines is GNAs the last row of the matrix;
the matrix formed is:
Figure GDA0003288551810000074
Xm×nan m ﹡ n-dimensional matrix constructed for the original signal; vm×nAn m ﹡ n-dimensional matrix constructed for the noise signal; if N is an even number, m is N/2+1, and N is N/2; if N is an odd number, m and N are both (N + 1)/2;
(4.5) performing singular value decomposition on H;
H=ΣWRT
w is unitary matrix with dimension m ﹡ m; r is a unitary matrix of n ﹡ n dimension, namely a left and right singular matrix of H, and T represents a transposed matrix of the matrix; element alpha of major diagonal line of m ﹡ n-dimensional diagonal matrix of sigmaiIs a non-zero singular value of H to increase the orderOrder, i.e. alpha1≥α2≥α3≥…≥αi
(4.6) determining the effective rank of sigma, namely the first l maximum singular values; approximating matrix Y for reconstruction Hl
Figure GDA0003288551810000081
WlIs the left singular vector corresponding to the first l largest singular values; rlIs the right singular vector corresponding to the first l largest singular values; sigmalThe diagonal matrix corresponding to the first l maximum singular values;
Figure GDA0003288551810000082
(4.7) mixing YlReconstructing the document components matched with the image information into a document matrix:
Figure GDA0003288551810000083
Figure GDA0003288551810000084
ε=min(l,γ-ε+l),γ=max(n,k);
w is the image information after denoising.
Searching the closest color value in the microorganism color table, and determining the index color corresponding to the scanned image to obtain a microorganism scanning result;
(5.1) dividing the low-contrast points;
Figure GDA0003288551810000085
χ=(x,y,σ)o(λ)
x and y are pixel coordinate values of the scanned image, and sigma is a scale parameter of the scanned image layer;
acquiring an extreme value Cn (x);
Figure GDA0003288551810000086
computing
Figure GDA0003288551810000087
If it is
Figure GDA0003288551810000088
If the point belongs to the ground contrast point, deleting the point;
(5.2) eliminating edge points;
constructing a scanning image HESSIAN matrix as follows:
Figure GDA0003288551810000089
Cijis the value of the point Cn with pixel coordinates (i, j);
calculating the determinant and the like of the matrix;
Sr(H)=Cxx+Cyy=α+β;
Bet(H)=CxxCyy-Cxy 2=αβ;
let a be θ β,
Figure GDA0003288551810000091
if the pixel point can not satisfy the formula, rejecting the pixel point;
and searching the closest color value of the pixel of the scanned image in the color table to determine the corresponding index color and determine the result of scanning the microorganism.
The matrix of spectrum scanning modules includes a scanning circuit,
the scanning circuit includes: a first resistor R1, a second resistor R2, a third resistor R3, a fourth resistor R4, a fifth resistor R5, a sixth resistor R6, a seventh resistor R7, an eighth resistor R8, a ninth resistor R9, a tenth resistor R10, an eleventh resistor R11, a twelfth resistor R12, a thirteenth resistor R13, a first capacitor C1, a second capacitor C2, a third capacitor C3, a fourth capacitor C4, a first diode L1, a second diode L2, a third diode L3, a first NPN transistor Q1, a second NPN transistor Q2, a third NPN transistor Q3, a PNP transistor P1, a power source VCC, a ground GND, a scanner S1, and an integrator S2;
the power supply VCC is respectively connected with one ends of a third resistor R3, a first capacitor C1, a fourth resistor R4 and a fifth resistor R5, and is also connected with a first end of an integrator S2, the other end of the third resistor R3 is respectively connected with a first end and a second end of a scanner S1, a third end of the scanner S1 is respectively connected with one end of the first resistor R1 and a third end of the integrator S2, and a fourth end of the scanner S1 is respectively connected with one end of the second resistor R2 and a fourth end of the integrator S2;
a second end of the integrator S2 is connected to one end of an eighth resistor R8, the other end of the eighth resistor R8 is connected to a base of a first NPN transistor Q1, and a fifth end of the integrator S2 is connected to the other end of a fourth resistor R4 and one end of a sixth resistor R6, respectively;
the other end of the fifth resistor R5 is connected to one end of a second capacitor C2, a seventh resistor R7 and a ninth resistor R9, and is further connected to the anode of the first diode L1 and the collector of the PNP transistor P1; the other end of the seventh resistor R7 is connected to the anode of a third diode L3, and the cathode of the third diode L3 is connected to the emitter of the first NPN transistor Q1 and the cathode of the first diode L1, respectively;
the base electrode of the PNP transistor P1 is connected to one end of a tenth resistor R10 and one end of a third capacitor C3, the other ends of the tenth resistor R10 and the third capacitor C3 are connected to one end of an eleventh resistor R11, the other end of the eleventh resistor R11 is connected to the base electrode of a third NPN transistor Q3, and the collector electrode of the third NPN transistor Q3 is connected to the negative electrode of a second diode L2;
an emitter of the PNP transistor P1 is connected to a collector of the second NPN transistor Q2, a base of the second NPN transistor Q2 is connected to the other end of the ninth resistor R9, one end of the fourth capacitor C4, one end of the twelfth resistor R12, and one end of the thirteenth resistor R13, respectively, and the other end of the twelfth resistor R12 is connected to an anode of the second diode L2;
the other ends of the first capacitor C1, the first resistor R1, the second resistor R2, the sixth resistor R6, the second capacitor C2, the fourth capacitor C4 and the thirteenth resistor R13 are grounded to GND, and the emitters of the first NPN transistor Q1, the second NPN transistor Q2 and the third NPN transistor Q3 are also grounded to GND.
A laboratory microorganism detection method specifically comprises the following steps:
(1) pre-constructing a color table according to the spectral data characteristics of a laboratory, comprising:
(1.1) constructing a spectral data set Q:
Q={Q1,Q2,Q3,…Qi…,Qn}
Qnobtaining the spectrum data for the nth time, wherein n is the total times of obtaining the spectrum data;
(1.2) acquiring a value of the spectral data at each time;
Qn=(Q1,n,Q2,n,Q3,n,…Qj,n,…,Qm,n)
Qm,nthe characteristic value is the mth spectral characteristic value when the spectral data is acquired at the nth time, and m is the total characteristic value quantity when the spectral data is acquired each time;
(1.3) carrying out standardization treatment;
Figure GDA0003288551810000101
Zm,nfor the purpose of the normalized value of the value,
Figure GDA0003288551810000102
for the mean, σ Q, of the n-th acquired spectral datanA variance for the nth acquired spectral data;
(1.4) constructing a confirmation color table;
Figure GDA0003288551810000103
Bmfor the mth spectral feature value of the constructed color chart, Q _1mIs the maximum of all the mth spectral characteristic values in the spectral data set Q;
(2) converting environmental scan results into spectral data, comprising the steps of:
the whole environment of the laboratory is optically scanned to obtain a series of polarized light, the light is reflected when entering a detection interface of the laboratory, and the reflected light is as follows:
Figure GDA0003288551810000104
Figure GDA0003288551810000106
is the included angle between the incident light of the polarized light and the S-polarization; ksAnd KpPredetermined coefficients of S-polarization and P-polarization, respectively, and KsAnd KpThe following conditions are satisfied;
Figure GDA0003288551810000105
k1 is the reflectance of polarized light in a laboratory environment; k2 is the reflection coefficient of the polarized light with the mycoderm, beta is the polarization coefficient of the polarized light, and beta is obtained by the following formula;
Figure GDA0003288551810000111
lambda is the refractive index of the detection surface;
the spectral data of the emergent light is:
Figure GDA0003288551810000112
θiis the polarized light and normal vectorF _ C is the spectrum data of the emergent light;
(3) converting the refractive index of the scanned position according to the spectral data; mapping index is carried out on the data of each position, the refractive index of each position is used for mapping with a refractive index comparison table, the comparison table is compared, and the refractive index difference is detected;
the imaging system outputs an image of the object as:
Figure GDA0003288551810000113
c is the imaging system channel number; f. ofc(x) Outputting a response value for the xth position of the C channel in the imaging system; rc(mu) is the spectral integrated response curve of the C channel; sigmac(μ) is the response curve of the light source spectrum of the C-th channel; dc(mu) spectral power curve of light source of C channel, Pc(μ) is the spectral transmittance curve of the pre-channel filter for the C-th channel, μ is the integrated parameter, with no practical meaning, x is the imaging system output object image position, C is 1, 2, 3 … … q, q is the total number of channels;
the output images of all channels are represented in a discrete matrix manner:
Figure GDA0003288551810000114
f (x) is the output image of all channels,
Figure GDA0003288551810000115
the spectral reflectance of the light-scanned image surface;
r (mu) is a diagonal matrix formed by the spectral comprehensive response curves of all channels;
Figure GDA0003288551810000116
σ (μ) is a diagonal matrix formed by response curves of the light source spectra of all channels;
Figure GDA0003288551810000121
d (mu) is a diagonal matrix formed by spectral power curves of light sources of all channels
Figure GDA0003288551810000122
P (mu) is a diagonal matrix formed by the spectral transmittance curves of the channel front filters of all channels;
Figure GDA0003288551810000123
calculating the mapping relation between the light scanning image and the color table through the inverse transformation of the positive image model of the spectral imaging system;
(5) denoising the scanned image file; comprises the following steps of;
(4.1) acquiring a scanned image file W;
(4.2) dividing the scanned image W into N blocks, the image W being N partial images, i.e., W ═ W1,W2,W3,…,Wi,…,WNAnd arbitrary local image WNAll satisfy the following formula;
WN=CSN+LBN
CSNpixel matrix, LB, of the original image of the Nth partial imageNA filtered pixel matrix for an nth image;
(4.3) solving for said WNThe singular characteristic quantity WV of the pixel ofNAnd said WNVariance σ ofN
(4.4) calculating an energy function of the local image;
Figure GDA0003288551810000124
wherein CSNIs the energy function of the local image, | WN-CSN||FIs WN-CSNF-norm, | | CSN||w*Is a weighted norm and meets the following requirements;
Figure GDA0003288551810000131
wherein j belongs to m and is a value of j, and m is a singular characteristic quantity WVNThe number of values contained, d is the sum of the local image WNThe Euclidean distance of less than 0.1, K is a preset value, | SVN|jThe original singular value is obtained by the following formula;
Figure GDA0003288551810000132
wherein, | WVN|jIs WVNThe jth value of (d);
(4.5) obtaining LB by the energy function of the partial imageN
Figure GDA0003288551810000133
The CS can be obtained by constructing an equation system by using the formulas in (4.5) and (4.2)NI.e. to the local part WNRemoving the filtered image, and removing the filtering of all the N local images to obtain the image from which the filtering is removed;
(1) the pre-constructing of the color table according to the spectral data characteristics of the laboratory comprises:
(1.1) extracting a color table of the image in the first clustering:
Q1={z1、z2、…zn};
zncollecting color points of a laboratory environment image, wherein n is the number of the color points;
(1.2) clustering for the second time to obtain an extended color table;
Figure GDA0003288551810000134
wherein σ is a spreading factor; and the secondary clustering refines the color table in the block. The association of colors and the diversity of color combinations within a block are maintained.
(1.3) carrying out standardization treatment;
Figure GDA0003288551810000135
zijis a normalized value, zijExpanding the color point value in the color table; alpha is the mean value of all sample data; β is the standard deviation of all sample data;
(1.4) carrying out brightness self-adaptation;
Figure GDA0003288551810000141
Itlis the mean value of brightness, Ct, of the color chartlIs the original brightness value, Pt, of the color chartlIs the mean value of the brightness, Im, of the color chartlAs the mean value of the brightness, Cm, of the imagelIs the original brightness value, Pm, of the imagelIs the contrast luminance mean of the image.
(2) The whole environment of the optical scanning laboratory converts the detection signals into spectral data;
scanning the whole environment of laboratory is a series of polarized light, and the reflection takes place when light incides laboratory detection interface, and the reverberation is:
Figure GDA0003288551810000142
Figure GDA0003288551810000143
is the polarization direction of a polarizerThe angle with the S polarization component; r issAnd rpPolarization coefficients for the S and P polarization components, respectively;
Figure GDA0003288551810000144
r01the polarization reflection coefficients of the laboratory environment and air; r is12The polarization reflection coefficients of the laboratory environment and the bacteria-carrying membrane are obtained;
delta is the polarized light phase difference;
Figure GDA0003288551810000145
niis the refractive index of the detection surface; thetaiAn incident angle of the detection light for the detection plane;
the spectral data of the emergent light is:
Figure GDA0003288551810000146
Figure GDA0003288551810000147
is the angle between the polarized light and the long axis.
(3) Converting the refractive index of the scanned position according to the spectral data; mapping and indexing the data of each position, mapping the refractive index of each position and a refractive index comparison table, comparing the comparison table and detecting the refractive index difference;
the imaging system outputs an image of the object as:
ck=∫λrk(λ)ρk(λ)sk(λ)o(λ)dλ;
k is the imaging system channel number; c. CkIs the output response of the k channel in the imaging system; r (λ) is the spectral response curve; s (lambda) is a response curve of the light source spectrum; o (λ) is the spectral power spectrum of the light source, ρk(λ) the spectral transmittance of the front filter of each channel;
expressed in a discrete matrix manner as:
Cn=(Rnρn)TSnRn;
dn is a multi-channel image output by the imaging system; sn is the spectral reflectivity of the surface of the optical scanning image; is a diagonal matrix with diagonal elements r (λ); the elements on the diagonal are the spectral responsivity of the imaging system at each wavelength;
Figure GDA0003288551810000148
tn is the spectral transmittance of the imaging system;
Figure GDA0003288551810000151
sn is a diagonal matrix taking the spectral power distribution of the light source as diagonal elements;
Figure GDA0003288551810000152
cn is an erect image model of the spectral imaging system;
and calculating the mapping relation between the light scanning image and the color table through the inverse transformation of the positive image model of the spectral imaging system.
(4) Denoising the scanned image file; comprises the following steps of;
(4.1) all image information documents g (t) { g ═ g1,g2,g3,…,gNConstructed as an m × n-order document matrix, giThe ith image information document being the font, image information document set g (t);
(4.2) setting the dimension n of the document matrix;
(4.3) extracting { g ] from G (t)1,g2,g3,…,gnAs the first row of the matrix;
(4.4) sequentially delaying backward by one document until the last signal of n lines is GNAs the last row of the matrix;
The matrix formed is:
Figure GDA0003288551810000153
Xm×nan m ﹡ n-dimensional matrix constructed for the original signal; vm×nAn m ﹡ n-dimensional matrix constructed for the noise signal; if N is an even number, m is N/2+1, and N is N/2; if N is an odd number, m and N are both (N + 1)/2;
(4.5) performing singular value decomposition on H;
H=ΣWRT
w is unitary matrix with dimension m ﹡ m; r is a unitary matrix of n ﹡ n dimension, namely a left and right singular matrix of H, and T represents a transposed matrix of the matrix; element alpha of major diagonal line of m ﹡ n-dimensional diagonal matrix of sigmaiNon-zero singular values of H, arranged in increasing order, i.e. alpha1≥α2≥α3≥…≥αi
(4.6) determining the effective rank of sigma, namely the first l maximum singular values; approximating matrix Y for reconstruction Hl
Figure GDA0003288551810000154
WlIs the left singular vector corresponding to the first l largest singular values; rlIs the right singular vector corresponding to the first l largest singular values; sigmalThe diagonal matrix corresponding to the first l maximum singular values;
Figure GDA0003288551810000155
(4.7) mixing YlReconstructing the document components matched with the image information into a document matrix:
Figure GDA0003288551810000161
Figure GDA0003288551810000162
ε=min(l,γ-ε+l),γ=max(n,k);
w is the image information after denoising.
(5) Searching the closest color value in the microorganism color table, and determining the index color corresponding to the scanned image to obtain a microorganism scanning result;
(5.1) dividing the low-contrast points;
Figure GDA0003288551810000163
χ=(x,y,σ)o(λ)
x and y are pixel coordinate values of the scanned image, and sigma is a scale parameter of the scanned image layer;
acquiring an extreme value Cn (x);
Figure GDA0003288551810000164
computing
Figure GDA0003288551810000165
If it is
Figure GDA0003288551810000166
If the point belongs to the ground contrast point, deleting the point;
(5.2) eliminating edge points;
constructing a scanning image HESSIAN matrix as follows:
Figure GDA0003288551810000167
Cijis the value of the point Cn with pixel coordinates (i, j);
calculating the determinant and the like of the matrix;
Sr(H)=Cxx+Cyy=α+β;
Bet(H)=CxxCyy-Cxy 2=αβ;
let a be θ β,
Figure GDA0003288551810000168
if the pixel point can not satisfy the formula, rejecting the pixel point;
and searching the closest color value of the pixel of the scanned image in the color table to determine the corresponding index color and determine the result of scanning the microorganism.
The invention has the beneficial effects that: the microorganism detection system or the detection method provided by the invention has the advantages that the color contrast data of the conventional environment is constructed as the basis, the detection image is obtained through polarized light scanning, and the abnormity of the laboratory environment is detected through the accurate denoising and contrast method, so that the system has higher precision, wider scanning range and more comprehensive detection.
Drawings
FIG. 1 is a schematic diagram of a laboratory microorganism detection system according to the present invention;
FIG. 2 is a schematic diagram of a laboratory microorganism detection method according to the present invention;
FIG. 3 is a circuit diagram of a scanning circuit of the laboratory microorganism detection system of the present invention.
Detailed Description
The invention is further described below with reference to fig. 1-2.
A laboratory microorganism detection system specifically comprises:
the building module is used for building a color table to be confirmed according to the spectral data characteristics of the laboratory;
the system comprises a scanning module, a data acquisition module and a data processing module, wherein the scanning module is used for carrying out optical scanning on the whole environment of a laboratory to obtain a corresponding environment scanning result and converting the environment scanning result into corresponding spectrum data;
the comparison module is used for acquiring the refractive index of a scanning position related to the overall environment of the laboratory scanned by light according to the spectral data acquired by the scanning module; searching and comparing the refractive index difference of each scanning position based on a prestored refractive index mapping table;
the image denoising module is used for denoising the image file to be scanned;
and the confirming module is used for searching a color value which is closest to the refractive index difference of each scanning position searched and compared by the comparison module based on the color table to be confirmed, which is constructed by the construction module, determining the index color corresponding to the image file to be scanned after the noise reduction processing is carried out by the image noise reduction module, and obtaining the microorganism scanning result.
(1) Pre-constructing a color table according to the spectral data characteristics of a laboratory, comprising:
(1.1) constructing a spectral data set Q:
Q={Q1,Q2,Q3,…Qi…,Qn}
Qnobtaining the spectrum data for the nth time, wherein n is the total times of obtaining the spectrum data;
(1.2) acquiring a value of the spectral data at each time;
Qn=(Q1,n,Q2,n,Q3,n,…Qj,n,…,Qm,n)
Qm,nthe characteristic value is the mth spectral characteristic value when the spectral data is acquired at the nth time, and m is the total characteristic value quantity when the spectral data is acquired each time;
(1.3) carrying out standardization treatment;
Figure GDA0003288551810000171
Zm,nfor the purpose of the normalized value of the value,
Figure GDA0003288551810000172
for the mean, σ Q, of the n-th acquired spectral datanA variance for the nth acquired spectral data;
(1.4) constructing a confirmation color table;
Figure GDA0003288551810000173
Bmfor the mth spectral feature value of the constructed color chart, Q _1mIs the maximum of all the mth spectral characteristic values in the spectral data set Q;
by using the above technology, a color table can be constructed through the acquired spectral data, and in the process of constructing the color table, the value ranges of the characteristic values of different positions of the spectral data are different, which may cause a large value range in the calculation process and greatly affect the result, so that the value range of the characteristic value causes a large error to the result, and in the process, the data is standardized, thereby determining the value ranges of the characteristic values of different positions of the spectral data to be a fixed range.
(2) Converting environmental scan results into spectral data, comprising the steps of:
the whole environment of the laboratory is optically scanned to obtain a series of polarized light, the light is reflected when entering a detection interface of the laboratory, and the reflected light is as follows:
Figure GDA0003288551810000181
Figure GDA0003288551810000186
is the included angle between the incident light of the polarized light and the S-polarization; ksAnd KpPredetermined coefficients of S-polarization and P-polarization, respectively, and KsAnd KpThe following conditions are satisfied;
Figure GDA0003288551810000182
k1 is the reflectance of polarized light in a laboratory environment; k2 is the reflection coefficient of the polarized light with the mycoderm, beta is the polarization coefficient of the polarized light, and beta is obtained by the following formula;
Figure GDA0003288551810000183
lambda is the refractive index of the detection surface;
the spectral data of the emergent light is:
Figure GDA0003288551810000184
θithe included angle between the polarized light and the normal vector is shown, and F _ C is spectrum data of emergent light;
by utilizing the technology, the environment scanning result can be automatically converted into the spectrum data corresponding to the environment through the polarized light, the incident light and the reflected light, so that the environment scanning result can be digitalized and the quantitative analysis can be better carried out.
(3) Converting the refractive index of the scanned position according to the spectral data; mapping index is carried out on the data of each position, the refractive index of each position is used for mapping with a refractive index comparison table, the comparison table is compared, and the refractive index difference is detected;
the imaging system outputs an image of the object as:
Figure GDA0003288551810000185
c is the imaging system channel number; f. ofc(x) Outputting a response value for the xth position of the C channel in the imaging system; rc(mu) is the spectral integrated response curve of the C channel; sigmac(μ) is the response curve of the light source spectrum of the C-th channel; dc(mu) spectral power curve of light source of C channel, Pc(μ) is the spectral transmittance curve of the pre-channel filter for the C-th channel, μ is the integrated parameter, with no practical meaning, x is the imaging system output object image position, C is 1, 2, 3 … … q, q is the total number of channels;
the output images of all channels are represented in a discrete matrix manner:
Figure GDA0003288551810000191
f (x) is the output image of all channels,
Figure GDA0003288551810000192
the spectral reflectance of the light-scanned image surface;
r (mu) is a diagonal matrix formed by the spectral comprehensive response curves of all channels;
Figure GDA0003288551810000193
σ (μ) is a diagonal matrix formed by response curves of the light source spectra of all channels;
Figure GDA0003288551810000194
d (mu) is a diagonal matrix formed by spectral power curves of light sources of all channels
Figure GDA0003288551810000195
P (mu) is a diagonal matrix formed by the spectral transmittance curves of the channel front filters of all channels;
Figure GDA0003288551810000201
calculating the mapping relation between the light scanning image and the color table through the inverse transformation of the positive image model of the spectral imaging system;
(5) denoising the scanned image file; comprises the following steps of;
(4.1) acquiring a scanned image file W;
(4.2) dividing the scanned image into WDividing into N blocks, and forming the image W into N partial images, namely W ═ W1,W2,W3,…,Wi,…,WNAnd arbitrary local image WNAll satisfy the following formula;
WN=CSN+LBN
CSNpixel matrix, LB, of the original image of the Nth partial imageNA filtered pixel matrix for an nth image;
(4.3) solving for the WNThe singular characteristic quantity WV of the pixel ofNAnd said WNVariance σ ofN
(4.4) calculating an energy function of the local image;
Figure GDA0003288551810000202
wherein, fCSNIs the energy function of the local image, | WN-CSN||FIs WN-CSNF-norm, | | CSN||w*Is a weighted norm and meets the following requirements;
Figure GDA0003288551810000203
wherein j belongs to m and is a value of j, and m is a singular characteristic quantity WVNThe number of values contained, d is the sum of the local image WNThe Euclidean distance of less than 0.1, K is a preset value, | SVN|jThe original singular value is obtained by the following formula;
Figure GDA0003288551810000204
wherein, | WVN|jIs WVNThe jth value of (d);
(4.5) obtaining LB by the energy function of the partial imageN
Figure GDA0003288551810000211
The CS can be obtained by constructing an equation system by using the formulas in (4.5) and (4.2)NI.e. to the local part WNRemoving the filtered image, and removing the filtering of all the N local images to obtain the image from which the filtering is removed;
with the above technique: the filtering of the image can be intelligently reduced, because the more similar matrixes are, the larger the singular value of the image is, the larger the information content of the image is, and the less the probability that the value is filtered is when the filtering matrix is calculated, so that more information can be reserved, and the original information is more reliable.
The pre-constructing of the color table according to the spectral data characteristics of the laboratory comprises:
(1.1) extracting a color table of the image in the first clustering:
Q1={z1、z2、…zn};
zncollecting color points of a laboratory environment image, wherein n is the number of the color points;
(1.2) clustering for the second time to obtain an extended color table;
Figure GDA0003288551810000212
wherein σ is a spreading factor; and the secondary clustering refines the color table in the block. The association of colors and the diversity of color combinations within a block are maintained.
(1.3) carrying out standardization treatment;
Figure GDA0003288551810000213
zijis a normalized value, zijExpanding the color point value in the color table; alpha is the mean value of all sample data; beta is all sample dataStandard deviation of (d);
(1.4) carrying out brightness self-adaptation;
Figure GDA0003288551810000214
Itlis the mean value of brightness, Ct, of the color chartlIs the original brightness value, Pt, of the color chartlIs the mean value of the brightness, Im, of the color chartlAs the mean value of the brightness, Cm, of the imagelIs the original brightness value, Pm, of the imagelIs the contrast luminance mean of the image.
Scanning the whole environment of laboratory is a series of polarized light, and the reflection takes place when light incides laboratory detection interface, and the reverberation is:
Figure GDA0003288551810000215
Figure GDA0003288551810000216
the included angle between the polarization direction of the polarizer and the S polarization component is formed; r issAnd rpPolarization coefficients for the S and P polarization components, respectively;
Figure GDA0003288551810000217
r01the polarization reflection coefficients of the laboratory environment and air; r is12The polarization reflection coefficients of the laboratory environment and the bacteria-carrying membrane are obtained;
delta is the polarized light phase difference;
Figure GDA0003288551810000221
niis the refractive index of the detection surface; thetaiAn incident angle of the detection light for the detection plane;
the spectral data of the emergent light is:
Figure GDA0003288551810000222
Figure GDA0003288551810000223
is the angle between the polarized light and the long axis.
Converting the refractive index of the scanned position according to the spectral data; mapping and indexing the data of each position, mapping the refractive index of each position and a refractive index comparison table, comparing the comparison table, and detecting the refractive index difference, including;
the imaging system outputs an image of the object as:
ck=∫λrk(λ)ρk(λ)sk(λ)o(λ)dλ;
k is the imaging system channel number; c. CkIs the output response of the k channel in the imaging system; r (λ) is the spectral response curve; s (lambda) is a response curve of the light source spectrum; o (λ) is the spectral power spectrum of the light source, ρk(λ) the spectral transmittance of the front filter of each channel;
expressed in a discrete matrix manner as:
Cn=(Rnρn)TSnRn;
dn is a multi-channel image output by the imaging system; sn is the spectral reflectivity of the surface of the optical scanning image; is a diagonal matrix with diagonal elements r (λ); the elements on the diagonal are the spectral responsivity of the imaging system at each wavelength;
Figure GDA0003288551810000224
tn is the spectral transmittance of the imaging system;
Figure GDA0003288551810000225
sn is a diagonal matrix taking the spectral power distribution of the light source as diagonal elements;
Figure GDA0003288551810000226
cn is an erect image model of the spectral imaging system;
and calculating the mapping relation between the light scanning image and the color table through the inverse transformation of the positive image model of the spectral imaging system.
Denoising the scanned image file; comprises the following steps of;
(4.1) all image information documents g (t) { g ═ g1,g2,g3,…,gNConstructed as an m × n-order document matrix, giThe ith image information document being the font, image information document set g (t);
(4.2) setting the dimension n of the document matrix;
(4.3) extracting { g ] from G (t)1,g2,g3,…,gnAs the first row of the matrix;
(4.4) sequentially delaying backward by one document until the last signal of n lines is GNAs the last row of the matrix;
the matrix formed is:
Figure GDA0003288551810000231
Xm×nan m ﹡ n-dimensional matrix constructed for the original signal; vm×nAn m ﹡ n-dimensional matrix constructed for the noise signal; if N is an even number, m is N/2+1, and N is N/2; if N is an odd number, m and N are both (N + 1)/2;
(4.5) performing singular value decomposition on H;
H=ΣWRT
w is unitary matrix with dimension m ﹡ m; r is a unitary matrix of n ﹡ n dimension, namely a left and right singular matrix of H, and T represents a transposed matrix of the matrix; element alpha of major diagonal line of m ﹡ n-dimensional diagonal matrix of sigmaiNon-zero singular values of H, arranged in increasing order, i.e. alpha1≥α2≥α3≥…≥αi
(4.6) determining the effective rank of sigma, namely the first l maximum singular values; approximating matrix Y for reconstruction Hl
Figure GDA0003288551810000232
WlIs the left singular vector corresponding to the first l largest singular values; rlIs the right singular vector corresponding to the first l largest singular values; sigmalThe diagonal matrix corresponding to the first l maximum singular values;
Figure GDA0003288551810000233
(4.7) mixing YlReconstructing the document components matched with the image information into a document matrix:
Figure GDA0003288551810000234
Figure GDA0003288551810000235
ε=min(l,γ-ε+l),γ=max(n,k);
w is the image information after denoising.
Searching the closest color value in the microorganism color table, and determining the index color corresponding to the scanned image to obtain a microorganism scanning result;
(5.1) dividing the low-contrast points;
Figure GDA0003288551810000236
χ=(x,y,σ)o(λ)
x and y are pixel coordinate values of the scanned image, and sigma is a scale parameter of the scanned image layer;
acquiring an extreme value Cn (x);
Figure GDA0003288551810000237
computing
Figure GDA0003288551810000241
If it is
Figure GDA0003288551810000242
If the point belongs to the ground contrast point, deleting the point;
(5.2) eliminating edge points;
constructing a scanning image HESSIAN matrix as follows:
Figure GDA0003288551810000243
Cijis the value of the point Cn with pixel coordinates (i, j);
calculating the determinant and the like of the matrix;
Sr(H)=Cxx+Cyy=α+β;
Bet(H)=CxxCyy-Cxy 2=αβ;
let a be θ β,
Figure GDA0003288551810000244
if the pixel point can not satisfy the formula, rejecting the pixel point;
and searching the closest color value of the pixel of the scanned image in the color table to determine the corresponding index color and determine the result of scanning the microorganism.
The spectral scan module matrix includes a scan circuit, as shown in figure 3,
the scanning circuit includes: a first resistor R1, a second resistor R2, a third resistor R3, a fourth resistor R4, a fifth resistor R5, a sixth resistor R6, a seventh resistor R7, an eighth resistor R8, a ninth resistor R9, a tenth resistor R10, an eleventh resistor R11, a twelfth resistor R12, a thirteenth resistor R13, a first capacitor C1, a second capacitor C2, a third capacitor C3, a fourth capacitor C4, a first diode L1, a second diode L2, a third diode L3, a first NPN transistor Q1, a second NPN transistor Q2, a third NPN transistor Q3, a PNP transistor P1, a power source VCC, a ground GND, a scanner S1, and an integrator S2;
the power supply VCC is respectively connected with one ends of a third resistor R3, a first capacitor C1, a fourth resistor R4 and a fifth resistor R5, and is also connected with a first end of an integrator S2, the other end of the third resistor R3 is respectively connected with a first end and a second end of a scanner S1, a third end of the scanner S1 is respectively connected with one end of the first resistor R1 and a third end of the integrator S2, and a fourth end of the scanner S1 is respectively connected with one end of the second resistor R2 and a fourth end of the integrator S2;
a second end of the integrator S2 is connected to one end of an eighth resistor R8, the other end of the eighth resistor R8 is connected to a base of a first NPN transistor Q1, and a fifth end of the integrator S2 is connected to the other end of a fourth resistor R4 and one end of a sixth resistor R6, respectively;
the other end of the fifth resistor R5 is connected to one end of a second capacitor C2, a seventh resistor R7 and a ninth resistor R9, and is further connected to the anode of the first diode L1 and the collector of the PNP transistor P1; the other end of the seventh resistor R7 is connected to the anode of a third diode L3, and the cathode of the third diode L3 is connected to the emitter of the first NPN transistor Q1 and the cathode of the first diode L1, respectively;
the base electrode of the PNP transistor P1 is connected to one end of a tenth resistor R10 and one end of a third capacitor C3, the other ends of the tenth resistor R10 and the third capacitor C3 are connected to one end of an eleventh resistor R11, the other end of the eleventh resistor R11 is connected to the base electrode of a third NPN transistor Q3, and the collector electrode of the third NPN transistor Q3 is connected to the negative electrode of a second diode L2;
an emitter of the PNP transistor P1 is connected to a collector of the second NPN transistor Q2, a base of the second NPN transistor Q2 is connected to the other end of the ninth resistor R9, one end of the fourth capacitor C4, one end of the twelfth resistor R12, and one end of the thirteenth resistor R13, respectively, and the other end of the twelfth resistor R12 is connected to an anode of the second diode L2;
the other ends of the first capacitor C1, the first resistor R1, the second resistor R2, the sixth resistor R6, the second capacitor C2, the fourth capacitor C4 and the thirteenth resistor R13 are grounded to GND, and the emitters of the first NPN transistor Q1, the second NPN transistor Q2 and the third NPN transistor Q3 are also grounded to GND.
The scanning circuit has the following beneficial effects: the purpose of spectrum scanning is conveniently achieved by arranging the scanner S1 and the integrator S2, the PNP transistor P1 and the second NPN transistor Q2 are arranged, the scanning circuit is conveniently protected, the possibility of damaging the scanning circuit or a device is reduced in the process of supplying power to the circuit, in addition, the scanned signal is further processed through a branch formed by the sixth resistor R6 and the fifth resistor R5, and the stability of the scanned signal is ensured.
A laboratory microorganism detection method specifically comprises the following steps:
(1) pre-constructing a color table according to the spectral data characteristics of a laboratory, comprising:
(1.1) constructing a spectral data set Q:
Q={Q1,Q2,Q3,…Qi…,Qn}
Qnobtaining the spectrum data for the nth time, wherein n is the total times of obtaining the spectrum data;
(1.2) acquiring a value of the spectral data at each time;
Qn=(Q1,n,Q2,n,Q3,n,…Qj,n,…,Qm,n)
Qm,nthe characteristic value is the mth spectral characteristic value when the spectral data is acquired at the nth time, and m is the total characteristic value quantity when the spectral data is acquired each time;
(1.3) carrying out standardization treatment;
Figure GDA0003288551810000251
Zm,nfor the purpose of the normalized value of the value,
Figure GDA0003288551810000252
for the mean, σ Q, of the n-th acquired spectral datanA variance for the nth acquired spectral data;
(1.4) constructing a confirmation color table;
Figure GDA0003288551810000253
Bmfor the mth spectral feature value of the constructed color chart, Q _1mIs the maximum of all the mth spectral characteristic values in the spectral data set Q;
(2) converting environmental scan results into spectral data, comprising the steps of:
the whole environment of the laboratory is optically scanned to obtain a series of polarized light, the light is reflected when entering a detection interface of the laboratory, and the reflected light is as follows:
Figure GDA0003288551810000254
Figure GDA0003288551810000267
is the included angle between the incident light of the polarized light and the S-polarization; ksAnd KpPredetermined coefficients of S-polarization and P-polarization, respectively, and KsAnd KpThe following conditions are satisfied;
Figure GDA0003288551810000261
k1 is the reflectance of polarized light in a laboratory environment; k2 is the reflection coefficient of the polarized light with the mycoderm, beta is the polarization coefficient of the polarized light, and beta is obtained by the following formula;
Figure GDA0003288551810000262
lambda is the refractive index of the detection surface;
the spectral data of the emergent light is:
Figure GDA0003288551810000263
θithe included angle between the polarized light and the normal vector is shown, and F _ C is spectrum data of emergent light;
(3) converting the refractive index of the scanned position according to the spectral data; mapping index is carried out on the data of each position, the refractive index of each position is used for mapping with a refractive index comparison table, the comparison table is compared, and the refractive index difference is detected;
the imaging system outputs an image of the object as:
Figure GDA0003288551810000264
c is the imaging system channel number; f. ofc(x) Outputting a response value for the xth position of the C channel in the imaging system; rc(mu) is the spectral integrated response curve of the C channel; sigmac(μ) is the response curve of the light source spectrum of the C-th channel; dc(mu) spectral power curve of light source of C channel, Pc(μ) is the spectral transmittance curve of the pre-channel filter for the C-th channel, μ is the integrated parameter, with no practical meaning, x is the imaging system output object image position, C is 1, 2, 3 … … q, q is the total number of channels;
the output images of all channels are represented in a discrete matrix manner:
Figure GDA0003288551810000265
f (x) is the output image of all channels,
Figure GDA0003288551810000266
the spectral reflectance of the light-scanned image surface;
r (mu) is a diagonal matrix formed by the spectral comprehensive response curves of all channels;
Figure GDA0003288551810000271
σ (μ) is a diagonal matrix formed by response curves of the light source spectra of all channels;
Figure GDA0003288551810000272
d (mu) is a diagonal matrix formed by spectral power curves of light sources of all channels
Figure GDA0003288551810000273
P (mu) is a diagonal matrix formed by the spectral transmittance curves of the channel front filters of all channels;
Figure GDA0003288551810000274
calculating the mapping relation between the light scanning image and the color table through the inverse transformation of the positive image model of the spectral imaging system;
(5) denoising the scanned image file; comprises the following steps of;
(4.1) acquiring a scanned image file W;
(4.2) dividing the scanned image W into N blocks, the image W being N partial images, i.e., W ═ W1,W2,W3,…,Wi,…,WNAnd arbitrary local image WNAll satisfy the following formula;
WN=CSN+LBN
CSNpixel matrix, LB, of the original image of the Nth partial imageNAs the Nth imageThe filtered pixel matrix of (2);
(4.3) solving for said WNThe singular characteristic quantity WV of the pixel ofNAnd said WNVariance σ ofN
(4.4) calculating an energy function of the local image;
Figure GDA0003288551810000281
wherein, fCSNIs the energy function of the local image, | WN-CSN||FIs WN-CSNF-norm, | | CSN||w*Is a weighted norm and meets the following requirements;
Figure GDA0003288551810000282
wherein j belongs to m and is a value of j, and m is a singular characteristic quantity WVNThe number of values contained, d is the sum of the local image WNThe Euclidean distance of less than 0.1, K is a preset value, | SVN|jThe original singular value is obtained by the following formula;
Figure GDA0003288551810000283
wherein, | WVN|jIs WVNThe jth value of (d);
(4.5) obtaining LB by the energy function of the partial imageN
Figure GDA0003288551810000284
The CS can be obtained by constructing an equation system by using the formulas in (4.5) and (4.2)NI.e. to the local part WNRemoving the filtered image, and removing the filtering of all the N local images to obtain the image from which the filtering is removed;
a laboratory microorganism detection method specifically comprises the following steps:
(1) the pre-constructing of the color table according to the spectral data characteristics of the laboratory comprises:
(1.1) extracting a color table of the image in the first clustering:
Q1={z1、z2、…zn};
zncollecting color points of a laboratory environment image, wherein n is the number of the color points;
(1.2) clustering for the second time to obtain an extended color table;
Figure GDA0003288551810000291
wherein σ is a spreading factor; and the secondary clustering refines the color table in the block. The association of colors and the diversity of color combinations within a block are maintained.
(1.3) carrying out standardization treatment;
Figure GDA0003288551810000292
zijis a normalized value, zijExpanding the color point value in the color table; alpha is the mean value of all sample data; β is the standard deviation of all sample data;
(1.4) carrying out brightness self-adaptation;
Figure GDA0003288551810000293
Itlis the mean value of brightness, Ct, of the color chartlIs the original brightness value, Pt, of the color chartlIs the mean value of the brightness, Im, of the color chartlAs the mean value of the brightness, Cm, of the imagelIs the original brightness value, Pm, of the imagelIs the contrast luminance mean of the image.
(2) The whole environment of the optical scanning laboratory converts the detection signals into spectral data;
scanning the whole environment of laboratory is a series of polarized light, and the reflection takes place when light incides laboratory detection interface, and the reverberation is:
Figure GDA0003288551810000294
Figure GDA0003288551810000295
the included angle between the polarization direction of the polarizer and the S polarization component is formed; r issAnd rpPolarization coefficients for the S and P polarization components, respectively;
Figure GDA0003288551810000296
r01the polarization reflection coefficients of the laboratory environment and air; r is12The polarization reflection coefficients of the laboratory environment and the bacteria-carrying membrane are obtained;
delta is the polarized light phase difference;
Figure GDA0003288551810000297
niis the refractive index of the detection surface; thetaiAn incident angle of the detection light for the detection plane;
the spectral data of the emergent light is:
Figure GDA0003288551810000298
Figure GDA0003288551810000299
is the angle between the polarized light and the long axis.
(3) Converting the refractive index of the scanned position according to the spectral data; mapping and indexing the data of each position, mapping the refractive index of each position and a refractive index comparison table, comparing the comparison table and detecting the refractive index difference;
the imaging system outputs an image of the object as:
ck=∫λrk(λ)ρk(λ)sk(λ)o(λ)dλ;
k is the imaging system channel number; c. CkIs the output response of the k channel in the imaging system; r (λ) is the spectral response curve; s (lambda) is a response curve of the light source spectrum; o (λ) is the spectral power spectrum of the light source, ρk(λ) the spectral transmittance of the front filter of each channel;
expressed in a discrete matrix manner as:
Cn=(Rnρn)TSnRn;
dn is a multi-channel image output by the imaging system; sn is the spectral reflectivity of the surface of the optical scanning image; is a diagonal matrix with diagonal elements r (λ); the elements on the diagonal are the spectral responsivity of the imaging system at each wavelength;
Figure GDA0003288551810000301
tn is the spectral transmittance of the imaging system;
Figure GDA0003288551810000302
sn is a diagonal matrix taking the spectral power distribution of the light source as diagonal elements;
Figure GDA0003288551810000303
cn is an erect image model of the spectral imaging system;
and calculating the mapping relation between the light scanning image and the color table through the inverse transformation of the positive image model of the spectral imaging system.
(4) Denoising the scanned image file; comprises the following steps of;
(4.1) all image information textGear g (t) { g1,g2,g3,…,gNConstructed as an m × n-order document matrix, giThe ith image information document being the font, image information document set g (t);
(4.2) setting the dimension n of the document matrix;
(4.3) extracting { g ] from G (t)1,g2,g3,…,gnAs the first row of the matrix;
(4.4) sequentially delaying backward by one document until the last signal of n lines is GNAs the last row of the matrix;
the matrix formed is:
Figure GDA0003288551810000304
Xm×nan m ﹡ n-dimensional matrix constructed for the original signal; vm×nAn m ﹡ n-dimensional matrix constructed for the noise signal; if N is an even number, m is N/2+1, and N is N/2; if N is an odd number, m and N are both (N + 1)/2;
(4.5) performing singular value decomposition on H;
H=ΣWRT
w is unitary matrix with dimension m ﹡ m; r is a unitary matrix of n ﹡ n dimension, namely a left and right singular matrix of H, and T represents a transposed matrix of the matrix; element alpha of major diagonal line of m ﹡ n-dimensional diagonal matrix of sigmaiNon-zero singular values of H, arranged in increasing order, i.e. alpha1≥α2≥α3≥…≥αi
(4.6) determining the effective rank of sigma, namely the first l maximum singular values; approximating matrix Y for reconstruction Hl
Figure GDA0003288551810000311
WlIs the left singular vector corresponding to the first l largest singular values; rlIs the right singular vector corresponding to the first l largest singular values; sigmalThe diagonal matrix corresponding to the first l maximum singular values;
Figure GDA0003288551810000312
(4.7) mixing YlReconstructing the document components matched with the image information into a document matrix:
Figure GDA0003288551810000313
Figure GDA0003288551810000314
ε=min(l,γ-ε+l),γ=max(n,k);
w is the image information after denoising.
(5) Searching the closest color value in the microorganism color table, and determining the index color corresponding to the scanned image to obtain a microorganism scanning result;
(5.1) dividing the low-contrast points;
Figure GDA0003288551810000315
χ=(x,y,σ)o(λ)
x and y are pixel coordinate values of the scanned image, and sigma is a scale parameter of the scanned image layer;
acquiring an extreme value Cn (x);
Figure GDA0003288551810000316
computing
Figure GDA0003288551810000317
If it is
Figure GDA0003288551810000318
If the point belongs to the ground contrast point, deleting the point;
(5.2) eliminating edge points;
constructing a scanning image HESSIAN matrix as follows:
Figure GDA0003288551810000319
Cijis the value of the point Cn with pixel coordinates (i, j);
calculating the determinant and the like of the matrix;
Sr(H)=Cxx+Cyy=α+β;
Bet(H)=CxxCyy-Cxy 2=αβ;
let a be θ β,
Figure GDA00032885518100003110
if the pixel point can not satisfy the formula, rejecting the pixel point;
and searching the closest color value of the pixel of the scanned image in the color table to determine the corresponding index color and determine the result of scanning the microorganism.
The microorganism detection system or the detection method provided by the invention has the advantages that the color contrast data of the conventional environment is constructed as the basis, the detection image is obtained through polarized light scanning, and the abnormity of the laboratory environment is detected through the accurate denoising and contrast method, so that the system has higher precision, wider scanning range and more comprehensive detection.
The above description is only a preferred embodiment of the present invention, but the scope of the present invention is not limited thereto, and any changes or substitutions that can be easily conceived by those skilled in the art within the technical scope of the present invention are included in the scope of the present invention. Therefore, the protection scope of the present invention shall be subject to the protection scope of the claims.

Claims (2)

1. A laboratory microorganism detection system for realizing a laboratory microorganism detection method is characterized by specifically comprising:
the building module is used for building a color table to be confirmed according to the spectral data characteristics of the laboratory;
the system comprises a scanning module, a data acquisition module and a data processing module, wherein the scanning module is used for carrying out optical scanning on the whole environment of a laboratory to obtain a corresponding environment scanning result and converting the environment scanning result into corresponding spectrum data;
the comparison module is used for acquiring the refractive index of a scanning position related to the overall environment of the laboratory scanned by light according to the spectral data acquired by the scanning module; searching and comparing the refractive index difference of each scanning position based on a prestored refractive index mapping table;
the image denoising module is used for denoising the image file to be scanned;
the confirmation module is used for searching a color value which is closest to the refractive index difference of each scanning position searched and compared by the comparison module based on the color table to be confirmed constructed by the construction module, determining an index color corresponding to the image file to be scanned after the noise reduction processing is carried out by the image noise reduction module, and obtaining a microorganism scanning result;
a laboratory microorganism detection method specifically comprises the following steps:
(1) pre-constructing a color table according to the spectral data characteristics of a laboratory, comprising:
(1.1) constructing a spectral data set Q:
Q={Q1,Q2,Q3,…Qi…,Qn}
Qnobtaining the spectrum data for the nth time, wherein n is the total times of obtaining the spectrum data;
(1.2) acquiring a value of the spectral data at each time;
Qn=(Q1,n,Q2,n,Q3,n,…Qj,n,…,Qm,n)
Qm,nthe characteristic value is the mth spectral characteristic value when the spectral data is acquired at the nth time, and m is the total characteristic value quantity when the spectral data is acquired each time;
(1.3) carrying out standardization treatment;
Figure FDA0003288551800000011
Zm,nfor the purpose of the normalized value of the value,
Figure FDA0003288551800000012
for the mean, σ Q, of the n-th acquired spectral datanA variance for the nth acquired spectral data;
(1.4) constructing a confirmation color table;
Figure FDA0003288551800000013
Bmfor the mth spectral feature value of the constructed color chart, Q _1mIs the maximum of all the mth spectral characteristic values in the spectral data set Q;
(2) converting environmental scan results into spectral data, comprising the steps of:
the whole environment of the laboratory is optically scanned to obtain a series of polarized light, the light is reflected when entering a detection interface of the laboratory, and the reflected light is as follows:
Figure FDA0003288551800000021
Figure FDA0003288551800000026
is the included angle between the incident light of the polarized light and the S-polarization; ksAnd KpPredetermined coefficients of S-polarization and P-polarization, respectively, and KsAnd KpThe following conditions are satisfied;
Figure FDA0003288551800000022
k1 is the reflectance of polarized light in a laboratory environment; k2 is the reflection coefficient of the polarized light with the mycoderm, beta is the polarization coefficient of the polarized light, and beta is obtained by the following formula;
Figure FDA0003288551800000023
lambda is the refractive index of the detection surface;
the spectral data of the emergent light is:
Figure FDA0003288551800000024
θithe included angle between the polarized light and the normal vector is shown, and F _ C is spectrum data of emergent light;
(3) converting the refractive index of the scanned position according to the spectral data; mapping index is carried out on the data of each position, the refractive index of each position is used for mapping with a refractive index comparison table, the comparison table is compared, and the refractive index difference is detected;
the imaging system outputs an image of the object as:
Figure FDA0003288551800000025
c is the imaging system channel number; f. ofc(x) Outputting a response value for the xth position of the C channel in the imaging system; rc(mu) is the spectral integrated response curve of the C channel; sigmac(μ) is the response curve of the light source spectrum of the C-th channel; dc(mu) spectral power curve of light source of C channel, Pc(μ) is the spectral transmittance curve of the pre-channel filter for the C-th channel, μ is the integrated parameter, with no practical meaning, x is the imaging system output object image position, C is 1, 2, 3 … … q, q is the total number of channels;
the output images of all channels are represented in a discrete matrix manner:
Figure FDA0003288551800000031
f (x) is the output image of all channels,
Figure FDA0003288551800000032
the spectral reflectance of the light-scanned image surface;
r (mu) is a diagonal matrix formed by the spectral comprehensive response curves of all channels;
Figure FDA0003288551800000033
σ (μ) is a diagonal matrix formed by response curves of the light source spectra of all channels;
Figure FDA0003288551800000034
d (mu) is a diagonal matrix formed by spectral power curves of light sources of all channels
Figure FDA0003288551800000035
P (mu) is a diagonal matrix formed by the spectral transmittance curves of the channel front filters of all channels;
Figure FDA0003288551800000036
calculating the mapping relation between the light scanning image and the color table through the inverse transformation of the positive image model of the spectral imaging system;
(4) denoising the scanned image file; comprises the following steps of;
(4.1) acquiring a scanned image file W;
(4.2) dividing the scanned image W into N blocks, wherein the image W is N partial images,W={W1,W2,W3,…,Wi,…,WNAnd arbitrary local image WNAll satisfy the following formula;
WN=CSN+LBN
CSNpixel matrix, LB, of the original image of the Nth partial imageNA filtered pixel matrix for an nth image;
(4.3) solving for the WNThe singular characteristic quantity WV of the pixel ofNAnd said WNVariance σ ofN
(4.4) calculating an energy function of the local image;
Figure FDA0003288551800000041
wherein, fCSNIs the energy function of the local image, | WN-CSN||FIs WN-CSNF-norm, | | CSN||w*Is a weighted norm and meets the following requirements;
Figure FDA0003288551800000042
wherein j belongs to m and is a value of j, and m is a singular characteristic quantity WVNThe number of values contained, d is the sum of the local image WNThe Euclidean distance of less than 0.1, K is a preset value, | SVN|jThe original singular value is obtained by the following formula;
Figure FDA0003288551800000043
wherein, | WVN|jIs WVNThe jth value of (d);
(4.5) obtaining LB by the energy function of the partial imageN
Figure FDA0003288551800000044
The CS can be obtained by constructing an equation system by using the formulas in (4.5) and (4.2)NI.e. to the local part WNRemoving the filtered image, and removing the filtering of all the N local images to obtain the image from which the filtering is removed;
(5) searching the closest color value in the microorganism color table, and determining the index color corresponding to the scanned image to obtain a microorganism scanning result;
(5.1) dividing the low-contrast points;
Figure FDA0003288551800000051
χ=(x,y,σ)o(λ)
x and y are pixel coordinate values of the scanned image, and sigma is a scale parameter of the scanned image layer;
acquiring an extreme value Cn (x);
Figure FDA0003288551800000052
computing
Figure FDA0003288551800000053
If it is
Figure FDA0003288551800000054
If the point belongs to the ground contrast point, deleting the point;
(5.2) eliminating edge points;
constructing a scanning image HESSIAN matrix as follows:
Figure FDA0003288551800000055
Cijis a point with pixel coordinate (i, j)A Cn value;
calculating the determinant and the like of the matrix;
Sr(H)=Cxx+Cyy=α+β;
Bet(H)=CxxCyy-Cxy 2=αβ;
let a be θ β,
Figure FDA0003288551800000056
if the pixel point can not satisfy the formula, rejecting the pixel point;
and searching the closest color value of the pixel of the scanned image in the color table to determine the corresponding index color and determine the result of scanning the microorganism.
2. The system of claim 1, wherein the spectral scanning module matrix comprises a scanning circuit,
the scanning circuit includes: a first resistor R1, a second resistor R2, a third resistor R3, a fourth resistor R4, a fifth resistor R5, a sixth resistor R6, a seventh resistor R7, an eighth resistor R8, a ninth resistor R9, a tenth resistor R10, an eleventh resistor R11, a twelfth resistor R12, a thirteenth resistor R13, a first capacitor C1, a second capacitor C2, a third capacitor C3, a fourth capacitor C4, a first diode L1, a second diode L2, a third diode L3, a first NPN transistor Q1, a second NPN transistor Q2, a third NPN transistor Q3, a PNP transistor P1, a power source VCC, a ground GND, a scanner S1, and an integrator S2;
the power supply VCC is respectively connected with one ends of a third resistor R3, a first capacitor C1, a fourth resistor R4 and a fifth resistor R5, and is also connected with a first end of an integrator S2, the other end of the third resistor R3 is respectively connected with a first end and a second end of a scanner S1, a third end of the scanner S1 is respectively connected with one end of the first resistor R1 and a third end of the integrator S2, and a fourth end of the scanner S1 is respectively connected with one end of the second resistor R2 and a fourth end of the integrator S2;
a second end of the integrator S2 is connected to one end of an eighth resistor R8, the other end of the eighth resistor R8 is connected to a base of a first NPN transistor Q1, and a fifth end of the integrator S2 is connected to the other end of a fourth resistor R4 and one end of a sixth resistor R6, respectively;
the other end of the fifth resistor R5 is connected to one end of a second capacitor C2, a seventh resistor R7 and a ninth resistor R9, and is further connected to the anode of the first diode L1 and the collector of the PNP transistor P1; the other end of the seventh resistor R7 is connected to the anode of a third diode L3, and the cathode of the third diode L3 is connected to the emitter of the first NPN transistor Q1 and the cathode of the first diode L1, respectively;
the base electrode of the PNP transistor P1 is connected to one end of a tenth resistor R10 and one end of a third capacitor C3, the other ends of the tenth resistor R10 and the third capacitor C3 are connected to one end of an eleventh resistor R11, the other end of the eleventh resistor R11 is connected to the base electrode of a third NPN transistor Q3, and the collector electrode of the third NPN transistor Q3 is connected to the negative electrode of a second diode L2;
an emitter of the PNP transistor P1 is connected to a collector of the second NPN transistor Q2, a base of the second NPN transistor Q2 is connected to the other end of the ninth resistor R9, one end of the fourth capacitor C4, one end of the twelfth resistor R12, and one end of the thirteenth resistor R13, respectively, and the other end of the twelfth resistor R12 is connected to an anode of the second diode L2;
the other ends of the first capacitor C1, the first resistor R1, the second resistor R2, the sixth resistor R6, the second capacitor C2, the fourth capacitor C4 and the thirteenth resistor R13 are grounded to GND, and the emitters of the first NPN transistor Q1, the second NPN transistor Q2 and the third NPN transistor Q3 are also grounded to GND.
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