WO2018103373A1 - Procédé et dispositif de reconnaissance et de comptage de molécules uniques - Google Patents

Procédé et dispositif de reconnaissance et de comptage de molécules uniques Download PDF

Info

Publication number
WO2018103373A1
WO2018103373A1 PCT/CN2017/098838 CN2017098838W WO2018103373A1 WO 2018103373 A1 WO2018103373 A1 WO 2018103373A1 CN 2017098838 W CN2017098838 W CN 2017098838W WO 2018103373 A1 WO2018103373 A1 WO 2018103373A1
Authority
WO
WIPO (PCT)
Prior art keywords
image
unit
bright spot
single molecule
intensity
Prior art date
Application number
PCT/CN2017/098838
Other languages
English (en)
Chinese (zh)
Inventor
徐伟彬
金欢
颜钦
姜泽飞
周志良
Original Assignee
深圳市瀚海基因生物科技有限公司
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 深圳市瀚海基因生物科技有限公司 filed Critical 深圳市瀚海基因生物科技有限公司
Priority to EP17205993.3A priority Critical patent/EP3336802B1/fr
Publication of WO2018103373A1 publication Critical patent/WO2018103373A1/fr

Links

Images

Classifications

    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B15/00ICT specially adapted for analysing two-dimensional or three-dimensional molecular structures, e.g. structural or functional relations or structure alignment
    • GPHYSICS
    • G06COMPUTING; CALCULATING OR COUNTING
    • G06VIMAGE OR VIDEO RECOGNITION OR UNDERSTANDING
    • G06V40/00Recognition of biometric, human-related or animal-related patterns in image or video data
    • G06V40/10Human or animal bodies, e.g. vehicle occupants or pedestrians; Body parts, e.g. hands
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B20/00ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B25/00ICT specially adapted for hybridisation; ICT specially adapted for gene or protein expression

Definitions

  • the invention relates to the field of gene sequencing technology, in particular to a single molecule identification, counting method, identification, counting device and processing system.
  • the third generation sequencing technology is single molecule sequencing
  • the single molecule sequencing technology based on imaging optical detection is a base recognition technology that relies on optical signals and electrical signals.
  • the fluorescence group is determined by fluorescence
  • the fluorescence emitted is the intensity of light emitted from the excited state to the ground state under laser irradiation of a specific power.
  • the difference in emitted light intensity, and the presence of background noise single-molecule recognition errors are caused.
  • the DNA strands are unevenly distributed, and the base clusters and the like also cause a decrease in effective single molecules.
  • the existing methods mainly rely on the human eye to perform single molecule recognition and counting on the collected fluorescent images, but such a method is labor-intensive and slow.
  • the method based on HMM and machine learning not only requires a large number of samples to be trained, but also has low operational efficiency.
  • the embodiments of the present invention aim to at least solve one of the technical problems existing in the prior art. Therefore, the embodiments of the present invention need to provide a single molecule identification, counting method, and identification and counting device.
  • a method for identifying a single molecule includes the steps of: inputting a time series of intensity of an image bright spot; forming a line graph of time and intensity of the bright spot of the image according to the time series, wherein the line graph is composed of multiple a line segment composition; meshing the line graphs to form a plurality of grids arranged in an array, counting the number of times of the line segments and/or the end points of the line segments that fall on each of the grids; The number of times corresponding to the grid, performing line etch on the line graph after meshing to convert the line graph after meshing into a simplified graph; performing run length encoding on the simplified graph To identify the connected area; calculate an area of each of the connected areas, and determine that one of the connected areas that satisfies the following condition corresponds to a single molecule: an area of the connected area is greater than a first set threshold.
  • the above-mentioned method for identifying a single molecule can be quickly recognized for a single molecule by converting
  • a single molecule counting method includes the steps of: inputting a time series of image bright point intensity; forming a line graph of time and intensity of the image bright point according to the time series, wherein the line graph is composed of multiple a line segment composition; meshing the line graphs to form a plurality of grids arranged in an array, counting the number of times of the line segments and/or the end points of the line segments that fall on each of the grids; The number of times corresponding to the grid, performing line etch on the line graph after meshing to convert the line graph after meshing into a simplified graph; performing run length encoding on the simplified graph To identify the connected area; calculate the area of each of the connected areas, and determine that one of the connected areas corresponding to the following condition corresponds to a single molecule: the area of the connected area is greater than a first set threshold; and the number of single molecules is calculated to be S2 .
  • the counting method of the single molecule described above is converted into image processing by a line graph of a time series of
  • a single molecule counting method includes the steps of: inputting a time series of image bright point intensity; forming a line graph of time and intensity of the image bright point according to the time series, wherein the line graph is composed of multiple a line segment composition; meshing the line graphs to form a plurality of grids arranged in an array, counting the number of times of the line segments and/or the end points of the line segments that fall on each of the grids; The number of times corresponding to the grid, performing line etch on the line graph after meshing to convert the line graph after meshing into a simplified graph; performing run length encoding on the simplified graph To identify the connected area; calculate the area of each of the connected areas, and determine that the following condition is satisfied, the count of the single molecule is increased by 1: the area of the connected area is greater than the first set threshold.
  • the counting method of the single molecule described above is converted into image processing by a line graph of a time series of bright spot intensity to obtain a histogram, and the single molecule can
  • a single molecule identification device for implementing one or all of the steps of the single molecule identification method of the above aspect of the present invention includes: an input unit for inputting a time series of image brightness intensity; and a conversion unit And a line graph for forming a time and an intensity of the image bright point according to the time series in the input unit, wherein the line graph is composed of a plurality of line segments; a grid statistical unit is configured to The line graph of the cells is meshed to form a plurality of grids arranged in an array, counting the number of times of the line segments and/or the end points of the line segments of each of the grids; a simplified unit for Performing line etching on the line graph after meshing according to the number of times corresponding to each of the grids to convert the line graph after meshing into a simplified graph; Performing run-length encoding on the simplified map to identify a connected area; determining a unit for calculating an area of each of the connected areas, and determining one of the connected areas that satisfies the following condition
  • a single molecule counting device for performing some or all of the steps of the single molecule counting method of the above aspect of the present invention, comprising: an input unit for inputting a time series of image brightness intensity; and a conversion unit And a line graph for forming a time and an intensity of the image bright point according to the time series in the input unit, wherein the line graph is composed of a plurality of line segments; a grid statistical unit is configured to The line graph of the cells is meshed to form a plurality of grids arranged in an array, counting the number of times of the line segments and/or the end points of the line segments of each of the grids; a simplified unit for Performing line etching on the line graph after meshing according to the number of times corresponding to each of the grids to convert the line graph after meshing into a simplified graph; Performing run-length encoding on the simplified map to identify a connected area; determining a unit for calculating an area of each of the connected areas, and determining one of the connected areas
  • a single molecule counting device for performing some or all of the steps of the single molecule counting method of the above aspect of the present invention, comprising: an input unit for inputting a time series of image brightness intensity; and a conversion unit And a line graph for forming a time and an intensity of the image bright point according to the time series in the input unit, wherein the line graph is composed of a plurality of line segments; a grid statistical unit is configured to The line graph of the cells is meshed to form a plurality of grids arranged in an array, counting the number of times of the line segments and/or the end points of the line segments of each of the grids; a simplified unit for Performing line etching on the line graph after meshing according to the number of times corresponding to each of the grids to convert the line graph after meshing into a simplified graph; Performing run-length encoding on the simplified map to identify a connected region; determining a unit for calculating an area of each of the connected regions, and determining that the count of the
  • a single molecule processing system includes: a data input device for inputting data; a data output device for outputting data; and a storage device for storing data, the data including a computer executable program; A processor for executing the computer executable program, the executing the computer executable program comprising performing the method of any of the above embodiments.
  • the single molecule processing system enables single molecule recognition and/or single molecule counting.
  • a computer readable storage medium for storing a program for execution by a computer, the method comprising executing the method of any of the above embodiments.
  • the computer readable storage medium may include read only memory, random access memory, magnetic or optical disks, and the like.
  • FIG. 1 is a schematic flow chart of a method for identifying a single molecule according to an embodiment of the present invention.
  • FIG. 2 is a schematic flow chart of another method for identifying a single molecule according to an embodiment of the present invention.
  • FIG. 3 is a schematic flow chart showing another method of identifying a single molecule according to an embodiment of the present invention.
  • FIG. 4 is a schematic flow chart showing another method of identifying a single molecule according to an embodiment of the present invention.
  • FIG. 5 is still another schematic flowchart of a method for identifying a single molecule according to an embodiment of the present invention.
  • FIG. 6 is a schematic flow chart showing another method of identifying a single molecule according to an embodiment of the present invention.
  • FIG. 7 is a schematic flow chart showing another method of identifying a single molecule according to an embodiment of the present invention.
  • FIG. 8 is still another schematic flow chart of a method for identifying a single molecule according to an embodiment of the present invention.
  • FIG. 9 is a schematic diagram showing a Mexican hat filter of a single molecule identification method according to an embodiment of the present invention.
  • FIG. 10 is a schematic flow chart of still another method for identifying a single molecule according to an embodiment of the present invention.
  • FIG. 11 is a schematic diagram of eight connected pixels in a single molecule identification method according to an embodiment of the present invention.
  • Fig. 12 is a schematic diagram showing a line graph of a single molecule identification method according to an embodiment of the present invention.
  • Fig. 13 is a schematic diagram showing the meshing of a line graph in the single molecule identification method according to the embodiment of the present invention.
  • Fig. 14 is a schematic diagram showing a line graph before filtering in the single molecule identification method according to the embodiment of the present invention.
  • Fig. 15 is a schematic diagram showing a filtered line graph in the single molecule identification method according to the embodiment of the present invention.
  • Fig. 16 is another schematic diagram of a line graph of a single molecule identification method according to an embodiment of the present invention.
  • Fig. 17 is a schematic diagram showing a histogram after equalization in the single molecule identification method according to the embodiment of the present invention.
  • Fig. 18 is a flow chart showing still another flow of the method for identifying a single molecule according to an embodiment of the present invention.
  • Fig. 19 is a schematic view showing the process of line corrosion in the single molecule identification method according to the embodiment of the present invention.
  • Fig. 20 is a schematic view showing another process of line corrosion in the single molecule identification method according to the embodiment of the present invention.
  • 21 is a schematic diagram of an 8-connected window in a single molecule identification method according to an embodiment of the present invention.
  • Fig. 22 is a schematic diagram showing the identification of a connected region in the single molecule identification method according to the embodiment of the present invention.
  • FIG. 23 is a schematic flow chart of a single molecule counting method according to an embodiment of the present invention.
  • Fig. 24 is a schematic flow chart showing another method of counting a single molecule according to an embodiment of the present invention.
  • Fig. 25 is a flow chart showing still another flow of the single molecule counting method according to the embodiment of the present invention.
  • Fig. 26 is a schematic flow chart showing still another method of counting a single molecule according to an embodiment of the present invention.
  • Figure 27 is a block diagram showing a single molecule identification device according to an embodiment of the present invention.
  • FIG. 28 is a block diagram showing still another module of the single molecule identification device according to the embodiment of the present invention.
  • 29 is a block diagram showing still another module of the single molecule identification device according to the embodiment of the present invention.
  • Figure 30 is a block diagram showing another module of the single molecule identification device of the embodiment of the present invention.
  • Figure 31 is still another block diagram of the single molecule identification device of the embodiment of the present invention.
  • 32 is another schematic block diagram of a single molecule identification device according to an embodiment of the present invention.
  • Figure 33 is a block diagram showing another module of the single molecule identification device of the embodiment of the present invention.
  • Figure 34 is a block diagram showing another module of the single molecule identification device of the embodiment of the present invention.
  • Figure 35 is a block diagram showing another module of the single molecule identification device of the embodiment of the present invention.
  • Figure 36 is a block diagram showing another module of the single molecule identification device of the embodiment of the present invention.
  • FIG. 37 is a schematic block diagram of a single molecule counting device according to an embodiment of the present invention.
  • 38 is a block diagram showing still another module of the single molecule counting device according to the embodiment of the present invention.
  • 39 is another schematic block diagram of a single molecule counting device according to an embodiment of the present invention.
  • 40 is still another block diagram of a single molecule counting device according to an embodiment of the present invention.
  • Fig. 41 is a block diagram showing still another module of the single molecule counting device according to the embodiment of the present invention.
  • Fig. 42 is a block diagram showing still another module of the single molecule counting device according to the embodiment of the present invention.
  • Figure 43 is a block diagram showing a single molecule processing system in accordance with an embodiment of the present invention.
  • first and second are used for descriptive purposes only and are not to be construed as indicating or implying a relative importance or implicitly indicating the number of technical features indicated.
  • features defining “first” or “second” may include one or more of the described features either explicitly or implicitly.
  • the meaning of "a plurality" is two or more unless specifically and specifically defined otherwise.
  • connection should be understood broadly, for example, it may be a fixed connection, a detachable connection, or an integral connection;
  • the mechanical connections may also be electrical connections or may communicate with each other; they may be directly connected or indirectly connected through an intermediate medium, and may be internal communication of two elements or an interaction relationship of two elements.
  • specific meanings of the above terms in the present invention can be understood on a case-by-case basis.
  • the single molecule identification method and counting method of the embodiments of the present invention can be applied to gene sequencing, and the "gene sequencing" and nucleic acid sequence determination, including DNA sequencing and/or RNA sequencing, including long fragment sequencing and / or short segment sequencing.
  • a single molecule identification method includes the steps of: S01, inputting a time series of image brightness intensity; and S02, forming a line graph of time and intensity of an image bright point according to a time series, a line chart It is composed of a plurality of line segments; S03, meshing the line graphs to form a plurality of grids arranged in the array, and counting the number of times of the line segments and/or end points of each line segment; S04, according to each network For the number of times corresponding to the grid, the line graph after meshing is subjected to line etching to convert the line graph after meshing into a simplified graph; S05, run-length encoding the simplified graph to identify the connected region; S06, calculating each The area of the connected area determines that one connected area satisfying the following condition corresponds to one single molecule: the area of the connected area is larger than the first set threshold.
  • the above single-molecule identification method converts the time-series line graph of the intensity of the bright spot into image processing to obtain the run-length coded communication.
  • the region can quickly identify single molecules, and the recognition accuracy is also high.
  • the single-molecule recognition method based on run-length coding can accurately identify a single molecule according to time series data of the intensity of a bright spot, and is particularly suitable for a case where the number of single molecules included in one bright spot is not more than 3.
  • step S01 when the image bright point is formed, the test sample is irradiated with laser light of a specific wavelength, the test sample is excited to emit fluorescence, and then the image formed by the fluorescence is collected by the camera, and the image is emitted corresponding to the test sample.
  • the image of the part is bright.
  • the so-called “bright spot” refers to the light-emitting point on the image, and one light-emitting point occupies at least one pixel.
  • the so-called "pixel” is the same as "pixel.”
  • the image is from a single molecule sequencing platform, such as the sequencing platform of Helicos, Pacific Biosciences (PacBio), and the input raw data is a parameter of the pixel point of the image, and the so-called "bright spot" is detected.
  • a single molecule sequencing platform such as the sequencing platform of Helicos, Pacific Biosciences (PacBio)
  • the input raw data is a parameter of the pixel point of the image, and the so-called "bright spot" is detected.
  • the single molecule identification method further includes: an image preprocessing step S31, the image preprocessing step analyzing the input image to be processed to obtain a first image, and the image to be processed includes at least one image. a bright spot, the image highlight has at least one pixel; the bright spot detecting step S32, the bright spot detecting step S32 includes the steps of: S321, analyzing the first image to calculate a bright spot determination threshold, S322, analyzing the first image to obtain a candidate bright spot, S323, determining according to the bright spot The threshold value determines whether the candidate bright spot is an image bright spot. If the determination result is yes, S324, the time series of the image bright spot intensity is acquired. If the determination result is no, S325, the candidate bright spot is discarded.
  • the denoising process of the image to be processed by the image preprocessing step can reduce the calculation amount of the bright spot detecting step, and at the same time, determine whether the candidate bright spot is an image bright point by using the bright spot judgment threshold, thereby improving the accuracy of determining the bright spot of the image.
  • the input image to be processed may be a 16-bit tiff format image of 512*512 or 2048*2048, and the image of the tiff format may be a grayscale image. In this way, the processing of the single molecule identification method can be simplified.
  • the image pre-processing step S31 includes performing background subtraction processing on the image to be processed to obtain a first image. In this way, the noise of the image to be processed can be further reduced, so that the accuracy of the single molecule counting method is higher.
  • the image pre-processing step S31 includes: performing a simplification process on the image to be processed after performing the background subtraction processing to obtain a first image. In this way, the amount of calculation of the subsequent single molecule recognition and/or counting method can be reduced.
  • the image pre-processing step S31 includes performing filtering processing on the image to be processed to obtain a first image. In this way, filtering the image to be processed can acquire the first image under the condition that the image detail features are retained as much as possible, thereby improving the accuracy of the single molecule recognition and/or counting method.
  • the image pre-processing step S31 includes: performing background subtraction processing on the image to be processed, and then performing filtering processing to obtain a first image.
  • the image to be processed is filtered after subtracting the background, which can further reduce the noise of the image to be processed, so that the accuracy of the single molecule recognition and/or counting method is higher.
  • the image pre-processing step S31 includes: performing a simplified process on the image to be processed after performing the subtractive background processing to obtain the first image. In this way, the amount of calculation of the subsequent image processing method can be reduced.
  • the image pre-processing step S31 includes performing a simplification process on the image to be processed to obtain a first image. In this way, the amount of calculation of the subsequent single molecule recognition and/or counting method can be reduced.
  • performing background subtraction processing on the image to be processed includes: determining an background of the image to be processed by using an open operation, and performing background subtraction processing on the image to be processed according to the background.
  • the open operation is used to eliminate small objects, separate objects at slender points, and smooth the boundaries of large objects without significantly changing the image area, so that the background-subtracted image can be acquired more accurately.
  • the image to be processed f(x, y) (such as a grayscale image) is moved by an a*a window (for example, a 15*15 window), and an open operation (corrosion re-expansion) is used to estimate
  • a*a window for example, a 15*15 window
  • an open operation corrosion re-expansion
  • g(x, y) is the grayscale image after etching
  • f(x, y) is the original grayscale image
  • B is the structural element
  • g(x, y) is the expanded grayscale image
  • f(x, y) is the original grayscale image
  • B is the structural element
  • the filtering process is a mexican hat filtering process.
  • Mexican hat filtering is easy to implement, reducing the cost of single-molecule identification and/or counting methods, while Mexican hat filtering improves foreground and background contrast, making the foreground brighter, making the background Darker.
  • the m*m window is used to perform Gaussian filtering on the image to be processed before the filtering process, and the Gaussian filtered image to be processed is subjected to two-dimensional Laplacian sharpening, where m is a natural number and is greater than 1. odd number.
  • m is a natural number and is greater than 1. odd number.
  • the Mexican hat core can be expressed as:
  • Equation 6 Gaussian filtering is performed on the image to be processed using the m*m window, as shown in Equation 6 below:
  • t1 and t2 represent the positions of the filtering window
  • wt1 and t2 represent the weights of the Gaussian filtering
  • Equation 7 The image to be processed is then subjected to two-dimensional Laplacian sharpening, as shown in Equation 7 below:
  • K and k both represent Laplacian operators, which are related to sharpening targets. If it is necessary to strengthen sharpening and weaken sharpening, modify K and k.
  • Equation 6 when performing Gaussian filtering, Equation 6 becomes:
  • the simplified image is a binarized image.
  • binarized images are easy to handle and have a wide range of applications.
  • the binarized image may include two values of 0 and 1 characterizing different attributes of the pixel, and the binarized image may be expressed as:
  • the signal to noise ratio matrix is obtained according to the image to be processed before the simplification processing, and the image to be processed before the processing is simplified according to the signal to noise ratio matrix to obtain the first image.
  • the image to be processed may be subjected to subtractive background processing, and then the signal to noise ratio matrix is obtained according to the image to be processed after subtracting the background processing.
  • the signal to noise ratio matrix is obtained according to the image to be processed after subtracting the background processing.
  • the signal to noise ratio matrix can be expressed as: Where x and y represent the coordinates of the pixel, h represents the height of the image, and w represents the width of the image, i ⁇ w, j ⁇ h.
  • the simplified image is a binarized image
  • the binarized image can be obtained from the signal to noise ratio matrix.
  • the binarized image is as shown in Equation 9:
  • the background image to be processed may be subjected to subtractive background processing and/or filtering processing.
  • the background subtraction background processing step and the filtering processing step of the above embodiment may be followed by subtracting the background processing to obtain the formula 4, and then subtracting the background.
  • the step of analyzing the first image to calculate a bright spot determination threshold comprises: processing the first image by the Otsu method to calculate a bright spot determination threshold.
  • the search for the bright spot determination threshold is realized by a more mature and simple method, thereby improving the The accuracy of the single molecule recognition and/or counting method and the cost of the single molecule recognition and/or counting method.
  • using the first image to perform the search of the bright spot determination threshold can improve the efficiency and accuracy of the single molecule recognition and/or counting method.
  • the Otsu method can also be called the maximum inter-class variance method.
  • the Otsu method uses the largest variance between classes to segment the image, which means that the probability of misclassification is the smallest and the accuracy is high.
  • the segmentation threshold of the foreground and background of the image to be processed is T
  • the ratio of the number of pixels belonging to the foreground to the entire image is ⁇ 0
  • the average gradation is ⁇ 0
  • the ratio of the number of pixels belonging to the background to the entire image is ⁇ 1
  • the average gray level is ⁇ 1 .
  • the total average gray level of the image to be processed is recorded as ⁇
  • the variance between classes is recorded as var, which is:
  • the traversal method is used to obtain a segmentation threshold T that maximizes the variance between classes, that is, the desired spot determination threshold T.
  • the step of determining whether the candidate bright spot is an image bright spot according to the bright spot determination threshold includes:
  • Step S41 searching for a pixel point larger than (h*h-1) in the first image and using the found pixel point as the center of the candidate bright point, h*h and the bright point are in one-to-one correspondence, in h*h Each value corresponds to one pixel, and h is a natural number and is an odd number greater than one;
  • Step S42 determining whether the center of the candidate bright spot satisfies the condition: I max *A BI *ceof guass >T, where I max is the center strongest intensity of the h*h window, and A BI is the first image in the h*h window
  • ceof guass is the correlation coefficient between the pixels of the h*h window and the two-dimensional Gaussian distribution
  • T is the bright point determination threshold.
  • I max can be understood as the center strongest intensity of the candidate bright spot.
  • h 3, looking for pixels that are greater than 8 connected, as shown in FIG. The found pixel point is used as the pixel point of the candidate bright spot.
  • I max is the strongest intensity in the center of the 3*3 window
  • a BI is the ratio of the set value in the first image in the 3*3 window
  • ceof guass is the correlation between the pixel of the 3*3 window and the two-dimensional Gaussian distribution. coefficient.
  • the first image is a simplified image, for example, the first image may be a binarized image, that is, the set value in the binarized image may be a value corresponding to when the pixel meets the set condition.
  • the binarized image may contain two values of 0 and 1 characterizing different attributes of the pixel, the set value is 1, and A BI is the ratio of 1 in the binarized image in the h*h window. .
  • SNR ⁇ mean(SNR)
  • BI 1.
  • the camera when acquiring the above image, sequentially performs fluorescence acquisition of a plurality of fields of view (FOV) in time series. Therefore, when image data is obtained, the intensity of the image highlights contained in the image data corresponds to the time series acquired by the camera.
  • FOV fields of view
  • step S02 after the desired image highlights are obtained, the intensity of the image highlights corresponding to the adjacent acquisition times are point-connected, and a line graph of the time and intensity of the image highlights is formed, as shown in FIG.
  • the horizontal axis represents the time at which fluorescence is collected, in milliseconds (ms)
  • the vertical axis represents the intensity of the image bright spot.
  • the time interval between two adjacent acquisitions of fluorescence is 20 ms.
  • the vertical axis is the corresponding bright point intensity value.
  • the bright spot intensity value is a bright pixel value
  • the bright pixel value is in the range of 0-65535
  • the 8-bit grayscale image The bright pixel values are in the range 0-255.
  • a 16-bit tiff image is used in the embodiment of the present invention.
  • step S03 the waveform of the line graph is converted into image processing for subsequent run length encoding.
  • Image processing of the line graph includes meshing the line graph.
  • meshing the line graph is divided by the number of time frames and the intensity of the acquisition intensity.
  • the line graph can be relatively simplely processed to obtain mesh division, which reduces the cost of the single molecule identification method.
  • it can be divided into M according to the number of time frames and N according to the size of the intensity, that is, M*N grids are formed.
  • the number of time frames of the acquired intensity is the time interval between two adjacent acquisitions of fluorescence.
  • a mesh may be referred to as a longitudinal direction along a horizontal axis and a height direction along a longitudinal axis.
  • the length of a grid can be set to several times the number of time frames, such as 1x, 2x, 2.5x, and so on.
  • the time interval between two adjacent acquisitions of fluorescence is 20 ms
  • the length of one grid is equal to one time interval
  • the height 0.02.
  • the number of segments falling on a grid can be 0, 1, or 2 times.
  • the black dots in Figure 16 represent the time series of the intensity of the image highlights.
  • the line graph is divided into 8*6 grids and the number of times that fall on the endpoints of each grid's line segments and/or line segments is counted.
  • the number of times of the line segment falling on each grid i.e., the number of times each grid is passed by the line segment
  • the number in the grid represents the number of lines falling on each grid.
  • the black dots in Figure 13 represent the time series of the intensity of the image highlights.
  • the structural element of the line such as the window size of W*1
  • the grid is marked as the first value, otherwise it is marked as the second value.
  • the meshed line graph can be converted into a simplified map including the first value and the second value.
  • the simplified map is a binarized map. If the first value is 1 and the second value is 0.
  • Figure 19 shows five grids arranged along the length. The numbers in the grid represent the number of times, then When performing line etching, the window is aligned with the grid. After the warp is etched, the five grids are labeled 0, 1, 0, 0, and 0, respectively.
  • Figure 20 shows five grids arranged along the length. The numbers in the grid represent the number of times. Then, when performing line etching, the window is staggered from the grid. After the warp is etched, the five grids are marked as 0, 1, 0, 0, and 0, respectively.
  • W is greater than or equal to the length of a grid.
  • W is an integer multiple of the length of a grid.
  • the threshold T has a value range of [6, 8], and its selection is related to the fluctuation of the waveform of the line graph. The smaller the fluctuation, the larger the value of the threshold T is.
  • an 8-connected approach can be used.
  • the respective connected areas are recursively connected according to the principle of 8 connections, and then the connected areas are identified by the run length coding.
  • 8 connectivity such as using the 3*3 window shown in FIG. 21
  • the grid will be The grid in the 8 directions of Q is identified as the same value as the grid Q, and so on.
  • Fig. 22 different connected areas are identified by different numerical values.
  • the number of occurrences of the same number is recorded as the area of the connected area, as shown in Fig. 22, the number of occurrences of the number 9 If it is 9, the area of the connected area corresponding to the number 9 is 9, and the number of occurrences of the number 7 is 20, and the area of the connected area corresponding to the number 7 is 20.
  • the first set threshold P has a value range of [5, 10].
  • the single molecule identification method further includes the steps of: S51, grouping according to the intensity, performing frequency statistics on the number of times to obtain a histogram; and S52, finding the maximum of the histogram.
  • S51 grouping according to the intensity, performing frequency statistics on the number of times to obtain a histogram
  • S52 finding the maximum of the histogram.
  • the peak at which a maximum point satisfying the following condition is determined corresponds to a single molecule: the value of the maximum point is greater than the second set threshold and the width of the peak at which the maximum point is located is greater than the third set threshold.
  • the single-molecule identification method can be applied to a wider range.
  • the single-molecule identification method based on the histogram can accurately identify a single molecule according to the time series data of the intensity of the bright spot, and is particularly suitable for the case where the number of single molecules included in the bright spot is >3.
  • in combination with histogram-based and run-length coding-based methods to identify single molecules it is possible to accurately identify single molecules in a line graph of various waveforms (time series of bright spot intensity).
  • step S51 includes the steps of dividing into N groups according to the magnitude of the strength, and counting the frequency of the statistics in the N groups: Where n i represents the sum of the frequencies of the number of times falling on the i-th row of the grid, j represents the number of time frames, gij represents the frequency of the number of times falling on the grid (i, j), and M represents the number of time frames.
  • n i represents the sum of the frequencies of the number of times falling on the i-th row of the grid, j represents the number of time frames, gij represents the frequency of the number of times falling on the grid (i, j), and M represents the number of time frames.
  • the horizontal axis of the histogram represents the number of groups
  • the vertical axis represents the frequency at which the number of times falls within the corresponding number of groups.
  • N is equal to the value of N formed in the M*N grids described above.
  • M is equal to the value of M described above which forms M*N grids.
  • the grouping is based on the magnitude of the intensity, and the frequency statistics are performed on the number of times to obtain a histogram.
  • the steps include: performing histogram equalization by the L window: Wherein, n p n i expressed equalization, n i 'denotes the size L of the equalization result and n i, p is an integer associated with the window, and where the i-th row. In this way, the distribution of the histogram can be made more uniform and easy to recognize.
  • the L window is used for histogram equalization.
  • the value of L is related to the decay rate of single-molecule fluorescence. Generally, if the single-molecule fluorescence is quenched quickly, the value of L should not be too large.
  • the accuracy of the histogram is affected by the size of the L window, and the value of L can be flexibly set to select the accuracy of the appropriate histogram. In one example, L has a value range of [5, 15].
  • FIG. 17 is an equalized histogram.
  • the horizontal axis of the histogram indicates the number of groups, and the vertical axis indicates the frequency at which the number of times falls within the corresponding number of groups.
  • step S52 all the maximum points of the histogram can be found by the derivative.
  • the second set threshold Q and the third set threshold H are related to the shape of the peak of the line graph. The sharper the peak, the larger the second set threshold Q is, and the third set threshold H is smaller; the peak is fatter, the first The second set threshold Q is smaller, and the third set threshold H is larger.
  • the second set threshold Q has a value range of [2, 6]
  • the third set threshold H has a value range of [4, 10].
  • the maximum point is the peak point, and the maximum point is the vertex (inflection point) of the peak, that is, the peak at which a maximum point satisfying the condition is judged corresponds to a single molecule.
  • the single molecule identification method prior to meshing the line graph, further includes the step of filtering the line graph.
  • FIG. 14 is a line diagram before filtering
  • FIG. 15 is a line diagram after filtering. It can be seen from the figure that the waveform of the filtered line chart is smoother, which is beneficial to improve. The accuracy and efficiency of single molecule recognition.
  • a single molecule counting method includes the steps of: S81, inputting a time series of image brightness intensity; S82, forming a line graph of time and intensity of an image bright point according to a time series, a line chart Consisting of a plurality of line segments; S83, meshing the line graphs to form a plurality of grids arranged in the array, and counting the number of times of the line segments and/or end points of each line segment; S84, according to each network For the number of times corresponding to the grid, the line graph after meshing is subjected to line etching to convert the line graph after meshing into a simplified graph; S85, run-length encoding the simplified graph to identify the connected region; S86, calculating each The area of the connected regions determines that one connected region satisfying the following condition corresponds to one single molecule: the area of the connected region is larger than the first set threshold; and S87, the number S2 of single molecules is calculated.
  • the counting method of the single molecule described above converts the time-series line graph of the intensity of the bright spot into image processing to obtain the running region of the run length encoding, and can quickly count the single molecules, and the counting accuracy is also high.
  • the description of the technical features and advantages of the single molecule identification and/or counting method in any of the above embodiments and examples includes explanations and explanations of steps, parameter settings, and image preprocessing bright spot detection, and the like. Also applicable to the single molecule counting method of the present embodiment, in order to avoid redundancy, it will not be developed in detail here.
  • the single molecule counting method prior to meshing the line graph in step S83, further includes the step of filtering the line graph.
  • the single molecule counting method further includes the steps of: S91, grouping according to the intensity, performing frequency statistics on the number of times to obtain a histogram; and S92, finding a histogram
  • the maximum value point determines that the peak of a maximum point satisfying the following condition corresponds to a single molecule: the value of the maximum point is greater than the second set threshold and the width of the peak where the maximum point is larger than the third setting
  • the threshold is determined; S93, the number of single molecules S1 is calculated; S94, and the smaller of S1 and S2 is taken as the final single molecule number.
  • the single-molecule counting method based on histogram is particularly suitable for accurately finding the single molecule number >3 of the bright spot
  • combining the two methods it is possible to accurately find and count single molecules in a line graph of various waveforms.
  • the simplified map is a binarized map.
  • a single molecule counting method includes the steps of: S61, inputting a time series of image brightness intensity; S62, forming a line graph of time and intensity of an image bright point according to a time series, a line chart Consisting of a plurality of line segments; S63, meshing the line graphs to form a plurality of grids arranged in the array, and counting the number of times of the line segments and/or end points of each line segment; S64, according to each network For the number of times corresponding to the grid, the line graph after the meshing is subjected to line etching to convert the line graph after the meshing into a simplified graph; S65, run-length encoding the simplified graph to identify the connected region; S66, calculating each When the area of the connected area is determined and it is determined that the following conditions are satisfied, the count of the single molecule is increased by one: the area of the connected area is larger than the first set threshold.
  • the counting method of the single molecule described above converts the time-series line graph of the intensity of the bright spot into image processing to obtain the running region of the run length encoding, and can quickly count the single molecules, and the counting accuracy is also high.
  • the single molecule counting method prior to meshing the line graph in step S63, further includes the step of filtering the line graph.
  • the single molecule counting method further includes steps. Step: S71, grouping according to the intensity, performing frequency statistics on the number of times to obtain a histogram; S72, finding the maximum point of the histogram, and determining that the single molecule is incremented by 1: maximum when the following conditions are met: The value of the point is greater than the second set threshold and the width of the peak at which the maximum point is located is greater than the third set threshold; S73, the count of the single molecule acquired based on the histogram and the count of the single molecule acquired based on the run length encoding The smaller is the final single molecule number. In this way, the single molecule counting method can be applied in a wider range, and a more accurate single molecule number can be obtained.
  • the two methods it is possible to accurately find and count single molecules in a line graph of various waveforms.
  • the number of single molecules acquired based on the histogram is S1
  • the number of single molecules acquired based on the run length encoding is S2
  • the sizes of S1 and S2 are compared, and the smaller ones of S1 and S2 are taken as the final single molecule number.
  • a single molecule identification device 200 is used to implement all or part of the steps of the single molecule identification method in any of the above embodiments or examples.
  • the molecular recognition device 200 includes: a first input unit 202 for inputting a time series of image brightness intensity; and a first conversion unit 204 configured to form a time and intensity of the image bright point according to the time sequence in the first input unit 202.
  • a line graph the line graph is composed of a plurality of line segments; a first grid statistic unit 206 is configured to mesh the line graphs from the first transform unit 204 to form a plurality of grids arranged in the array, and the statistics fall on each The number of times of the line segments and/or the end points of the line segments; the first simplification unit 208 is configured to perform line etching on the meshed line graphs according to the number of times corresponding to each mesh to perform meshing The subsequent line graph is converted into a simplified map; a first identifying unit 209 is configured to run-length encode the simplified graph to identify a connected region; and a first determining unit 210 is configured to calculate each connected region.
  • the single-molecule identification device 200 converts a time-series line graph of bright spot intensity into image processing to obtain a run-length coded connected region, and can quickly recognize a single molecule, and the recognition accuracy is also high.
  • the simplified map is a binarized map.
  • the single molecule identification device 200 further includes a first filtering unit 212 coupled to the first mesh statistics unit 206 for meshing the line graphs.
  • the line graph from the first conversion unit 204 is filtered.
  • meshing the line graph is divided according to the number of time frames of the acquisition intensity and the magnitude of the intensity.
  • the single molecule identification device 200 further includes: a first histogram statistic unit 214 for grouping based on the magnitude of the intensity, and performing frequency statistics on the number of times from the grid statistical unit. Obtaining a histogram; in the first determining unit 210, finding a maximum point of the histogram from the histogram, and determining that a peak of a maximum point satisfying the following condition corresponds to a single molecule: a maximum value The value of the point is greater than the second set threshold and the width of the peak at which the maximum point is located is greater than the third set threshold.
  • the first histogram statistic unit 214 grouping is performed based on the magnitude of the intensity, and frequency statistics are performed on the number of times to obtain a histogram, including: dividing into N groups according to the magnitude of the intensity, and the number of statistics falls in Frequency in N groups: Where n i represents the sum of the frequencies of the number of times falling on the i-th row of the grid, j represents the number of time frames, g ij represents the frequency of the number of times falling on the grid (i, j), and M represents the number of time frames Quantity.
  • the first histogram statistic unit 214 grouping is performed based on the magnitude of the intensity, and frequency statistics are performed on the number of times to obtain a histogram including: performing histogram equalization by the L window: Wherein, n p n i expressed equalization, n i 'denotes the size L of the equalization result and n i, p is an integer associated with the window, and where the i-th row.
  • the single-molecule identification device 200 further includes: a first image pre-processing unit 218 for analyzing the input image to be processed to obtain a first image.
  • the image to be processed includes at least one image bright point, the image bright spot has at least one pixel point;
  • the first bright spot detecting unit 220 is configured to: analyze the first image to calculate a bright spot determination threshold, analyze the first image to obtain The candidate bright spot determines whether the candidate bright spot is an image bright spot according to the bright spot determination threshold. If the determination result is yes, the time series of the image bright spot intensity is acquired, and if the determination result is negative, the candidate bright spot is discarded.
  • the first image pre-processing unit 218 includes a first subtraction background unit 226 for performing background subtraction processing on the image to be processed to obtain a first image.
  • the first image pre-processing unit 218 includes a first image reduction unit 222 for simplifying the image to be processed after performing the background subtraction process. Obtain the first image.
  • the first image pre-processing unit 218 includes a first image filtering unit 224, the first image.
  • the image filtering unit 224 performs filtering processing on the image to be processed to obtain a first image.
  • the first image pre-processing unit 218 includes a first subtraction background unit 226 and a first image filtering unit 224, and the first subtraction background unit 226 is configured to perform background subtraction processing on the image to be processed.
  • the first image filtering unit 224 is configured to perform filtering processing on the image to be processed after performing the subtractive background processing to obtain a first image.
  • the first image pre-processing unit 218 includes a first image reduction unit 222, and the first image reduction unit 222 is configured to perform image processing on the image after performing background subtraction processing. Simplification is performed to obtain a first image.
  • the first image pre-processing unit 218 includes a first image reduction unit 222 for performing a simplified process on the image to be processed to obtain a first image.
  • performing background subtraction processing on the image to be processed includes: determining an background of the image to be processed by using an open operation, and performing background subtraction processing on the image to be processed according to the background.
  • the filtering process is a mexican hat filtering process.
  • the simplification process is a binarization process.
  • the first image reduction unit 222 is configured to acquire a signal to noise ratio matrix according to the image to be processed before the simplified processing, and simplify the simplified image before processing according to the signal to noise ratio matrix to obtain the first image.
  • analyzing the first image to calculate the bright spot determination threshold comprises: processing the first image by the Otsu method to calculate a bright spot determination threshold.
  • determining, in the first bright spot detecting unit 220, whether the candidate bright spot is an image bright point according to the bright spot determination threshold includes: searching for a pixel point larger than (h*h-1) in the first image and The found pixel is the center of the candidate bright spot, h is a natural number and is an odd number greater than 1; determining whether the center of the candidate bright spot satisfies the condition: I max *A BI *ceof guass >T, where I max is h*h window The strongest intensity of the center, A BI is the ratio of the set value in the first image in the h*h window, ceof guass is the correlation coefficient of the pixel of the h*h window and the two-dimensional Gaussian distribution, and T is the bright point decision threshold If the above conditions are met, it is determined that the bright spot corresponding to the center of the candidate bright spot is an image bright spot, and if the above condition is not satisfied, the bright spot corresponding to the center of the candidate bright spot is
  • a single molecule counting device 400 is used to implement all or part of the single molecule counting method in any of the above embodiments and examples of the present invention.
  • the single-molecule counting device 400 includes: a second input unit 402 for inputting a time series of image brightness intensity; and a second converting unit 404, configured to form an image bright spot according to a time sequence in the second input unit 402. a line graph of time and intensity, the line graph is composed of a plurality of line segments; the second grid statistics unit 406 is configured to mesh the line graphs from the second transforming unit 404 to form a plurality of grids arranged in the array.
  • the second simplifying unit 408 is configured to perform line etching on the meshed line graph according to the number of times corresponding to each grid
  • the meshed map is converted into a simplified map
  • the second identifying unit 409 is configured to run-length encode the simplified graph to identify the connected region
  • the second determining unit 410 is configured to calculate each Area of the through region is determined to satisfy the following conditions corresponding to a communication area of a single molecule: a first area of the communication region is greater than the set threshold value; calculating unit 412 for calculating the number of monomolecular obtaining S2.
  • the single-molecule counting device 400 converts a time-series line graph of bright spot intensity into image processing to obtain a run-length coded connected region, and can quickly count a single molecule, and the counting accuracy is also high.
  • the single molecule counting device 400 further includes a second filtering unit 414 coupled to the second mesh statistical unit 406 for meshing the line graph before it is meshed.
  • the line graph from the second conversion unit 404 is filtered.
  • the single molecule counting device 400 further includes: a second histogram counting unit 416 for grouping based on the magnitude of the intensity, and counting the number of times from the second grid statistical unit 406. Frequency statistics to obtain a histogram; in the second determining unit 410, find a maximum value point of the histogram from the second histogram statistic unit 416, and determine that a peak of a maximum value point satisfying the following condition corresponds to a single Molecule: the value of the maximum value point is greater than the second set threshold value and the width of the peak at which the maximum value point is located is greater than the third set threshold value; in the calculation unit 412, the number S1 of single molecules is calculated, and the numbers S1 and S2 are taken. The smaller one is the final single molecule number.
  • a single molecule counting device 600 includes: a third input unit 602 for inputting a time series of image brightness intensity; and a third converting unit 604 for using a third input unit.
  • a time series in 602 a line graph of time and intensity of the image highlights, the line graph consisting of a plurality of line segments; and a third grid statistics unit 606 for meshing the line graphs from the third transforming unit 604 Forming a plurality of grids arranged in an array, counting the number of times of the line segments and/or the end points of the line segments of each grid; and a third simplifying unit 608 for performing grids according to the number of times corresponding to each grid
  • the divided line graph performs line etching to convert the meshed line graph into a simplified map;
  • the third identifying unit 609 is configured to run-length encode the simplified map to identify the connected region; and the third determining unit 610 is configured to: Calculate the area of each connected area and determine that it is satisfied In the
  • the single-molecule counting device 600 converts the time-series line graph of the intensity of the bright spot into image processing to obtain the run-length coded connected region, and can quickly count the single molecules, and the counting accuracy is also high.
  • the single molecule counting device 600 further includes a third filtering unit 612 coupled to the third mesh statistical unit 606 for meshing the line graph before it is meshed.
  • the line graph from the third conversion unit 604 is filtered.
  • the single-molecule counting device 600 further includes: a third histogram statistic unit 614 for grouping based on the magnitude of the intensity, and counting the number of times from the third grid statistical unit 606.
  • the frequency statistics are obtained to obtain a histogram; in the third determining unit 610, the maximum value point of the histogram from the third histogram statistic unit 614 is searched, and when the following condition is satisfied, the count of the single molecule is added: The value of the value point is greater than the second set threshold and the width of the peak at which the maximum value point is greater than the third set threshold; and the count of the single molecule acquired based on the histogram and the count of the single molecule acquired based on the run length encoding The smaller is the final single molecule number.
  • a single molecule processing system 300 includes: a data input device 302 for inputting data; a data output device 304 for outputting data; and a storage device 306 for storing data and data.
  • a computer executable program is included; a processor 308 for executing a computer executable program, and executing the computer executable program includes the method of performing any of the above embodiments.
  • a computer readable storage medium for storing a program for execution by a computer, the program comprising the method of any of the above embodiments.
  • the computer readable storage medium may include read only memory, random access memory, magnetic or optical disks, and the like.
  • each functional unit in each embodiment of the present invention may be integrated into one processing module, or each unit may exist physically separately, or two or more units may be integrated into one module.
  • the above integrated modules can be implemented in the form of hardware or in the form of software functional modules.
  • the integrated modules, if implemented in the form of software functional modules and sold or used as stand-alone products, may also be stored in a computer readable storage medium.

Landscapes

  • Physics & Mathematics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Theoretical Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Computational Biology (AREA)
  • Biotechnology (AREA)
  • Evolutionary Biology (AREA)
  • Biophysics (AREA)
  • Medical Informatics (AREA)
  • Chemical & Material Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Molecular Biology (AREA)
  • Analytical Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Human Computer Interaction (AREA)
  • General Physics & Mathematics (AREA)
  • Multimedia (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
  • Image Analysis (AREA)

Abstract

L'invention concerne un procédé de reconnaissance et de comptage de molécules uniques et un dispositif de reconnaissance et de comptage. Le procédé de reconnaissance de molécules uniques comprend les étapes suivantes consistant à : entrer une séquence temporelle d'intensité d'un point lumineux d'image (S01) ; former un graphique en segments de temps et d'intensité du point lumineux d'image conformément à la séquence temporelle, le graphique en segments étant composé d'une pluralité de segments de ligne (S02) ; appliquer une division de grille au graphique en segments de façon à former une pluralité de grilles organisées en un réseau, et compter le nombre de fois où les segments de ligne et/ou les points d'extrémité des segments de ligne tombent sur chacune des grilles (S03) ; appliquer une érosion de lignes au graphique en segments après la division de grille conformément au nombre de fois correspondant à chaque grille de façon à convertir le graphique en segments obtenu après la division de grille en un graphique simplifié (S04) ; appliquer un codage par longueur de plage au graphique simplifié de façon à identifier des régions de connexion (S05) ; et calculer la zone de chaque région de connexion, puis déterminer une molécule unique correspondant à l'une des régions de connexion qui satisfait à la condition suivante : la zone de la région de connexion est supérieure à un premier seuil défini (S06). Le procédé de reconnaissance de molécules uniques permet une reconnaissance rapide d'une molécule unique par une conversion d'un graphique en segments d'une séquence temporelle de l'intensité d'un point lumineux en traitement d'image de façon à obtenir un histogramme, et la précision de reconnaissance du procédé est élevée.
PCT/CN2017/098838 2016-12-09 2017-08-24 Procédé et dispositif de reconnaissance et de comptage de molécules uniques WO2018103373A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP17205993.3A EP3336802B1 (fr) 2016-12-09 2017-12-07 Procédé et dispositif pour identifier une molécule unique à partir d'une image et procédé et dispositif pour compter une molécule unique à partir d'une image

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201611129604.1 2016-12-09
CN201611129604 2016-12-09

Publications (1)

Publication Number Publication Date
WO2018103373A1 true WO2018103373A1 (fr) 2018-06-14

Family

ID=62490673

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2017/098838 WO2018103373A1 (fr) 2016-12-09 2017-08-24 Procédé et dispositif de reconnaissance et de comptage de molécules uniques

Country Status (2)

Country Link
CN (1) CN108229098A (fr)
WO (1) WO2018103373A1 (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020037570A1 (fr) 2018-08-22 2020-02-27 深圳市真迈生物科技有限公司 Procédé et dispositif de recalage d'images et produit de programme informatique
CN112288783B (zh) * 2018-08-22 2021-06-29 深圳市真迈生物科技有限公司 基于图像构建测序模板的方法、碱基识别方法和装置
EP3843034A4 (fr) 2018-08-22 2021-08-04 GeneMind Biosciences Company Limited Procédé et dispositif de détection de points brillants sur une image, et produit programme d'ordinateur
EP3843033B1 (fr) * 2018-08-22 2024-05-22 GeneMind Biosciences Company Limited Procédé de construction de modèle de séquençage sur la base d'une image, et procédé et dispositif de reconnaissance de bases
CN110874821B (zh) * 2018-08-31 2023-05-30 赛司医疗科技(北京)有限公司 一种自动过滤精液中非精子成分的图像处理方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105243677A (zh) * 2015-09-02 2016-01-13 华中科技大学 一种保证精度的实时单分子定位方法及系统
CN105303551A (zh) * 2015-08-07 2016-02-03 深圳市瀚海基因生物科技有限公司 一种单分子定位方法
CN105303540A (zh) * 2015-08-14 2016-02-03 深圳市瀚海基因生物科技有限公司 一种单分子图像纠偏装置

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100570337C (zh) * 2005-12-16 2009-12-16 中国科学院上海光学精密机械研究所 膜蛋白分子相互作用的光学探测方法
CA2737116C (fr) * 2008-09-16 2019-01-15 Historx, Inc. Quantification reproductible de l'expression de biomarqueurs
US8532398B2 (en) * 2010-03-26 2013-09-10 General Electric Company Methods and apparatus for optical segmentation of biological samples
CN103236052B (zh) * 2013-03-28 2014-05-07 华中科技大学 一种基于l1最小化模型的全自动细胞定位方法

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105303551A (zh) * 2015-08-07 2016-02-03 深圳市瀚海基因生物科技有限公司 一种单分子定位方法
CN105303540A (zh) * 2015-08-14 2016-02-03 深圳市瀚海基因生物科技有限公司 一种单分子图像纠偏装置
CN105243677A (zh) * 2015-09-02 2016-01-13 华中科技大学 一种保证精度的实时单分子定位方法及系统

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
LV WEI: "Single molecule fluorescence fluctuations of the cyanine dyes linked covalently to DNA", SCIENCE IN CHINA SERIES B: CHEMISTRY, 31 August 2009 (2009-08-31) *
YU ET AL: "Fast Fourier-Domain Localization Algorithm of Single Molecule with Nanometer Resolution for Super-Resolution Fluorescence Imaging", ACTA OPTICA SINICA, vol. 32, no. 2, 29 February 2012 (2012-02-29), pages 0218001-1 - 0218001-6, XP055607036 *

Also Published As

Publication number Publication date
CN108229098A (zh) 2018-06-29

Similar Documents

Publication Publication Date Title
WO2018103373A1 (fr) Procédé et dispositif de reconnaissance et de comptage de molécules uniques
CN107918931B (zh) 图像处理方法及系统及计算机可读存储介质
Yousif et al. Toward an optimized neutrosophic K-means with genetic algorithm for automatic vehicle license plate recognition (ONKM-AVLPR)
CN111524137B (zh) 基于图像识别的细胞识别计数方法、装置和计算机设备
CN114419025A (zh) 一种基于图像处理的纤维板质量评估方法
JP6517788B2 (ja) 適応的病理組織画像分解のためのシステム及び方法
CN109903282B (zh) 一种细胞计数方法、系统、装置和存储介质
Abdelkader et al. A multi-objective invasive weed optimization method for segmentation of distress images
CN117078671A (zh) 一种甲状腺超声影像智能分析系统
CN115294377A (zh) 一种道路裂缝的识别系统及方法
WO2018103345A1 (fr) Procédé et dispositif de reconnaissance et de comptage de molécule unique
CN117237198A (zh) 基于深度学习的超分辨测序方法及装置、测序仪及介质
US10303847B2 (en) Single molecule identification using intensity time sequencing, line charting and run-length coding
CN115187878A (zh) 基于无人机图像分析的风力发电装置叶片缺陷检测方法
CN113506312A (zh) 一种紫外放电图像分割方法及计算机可读介质
CN114693539A (zh) 一种基于荧光图片的pcr数据处理与曲线拟合方法及pcr仪器
Jule et al. Micrarray Image Segmentation Using Protracted K-Means Net Algorithm in Enhancement of Accuracy and Robustness
EP3336802B1 (fr) Procédé et dispositif pour identifier une molécule unique à partir d'une image et procédé et dispositif pour compter une molécule unique à partir d'une image
Darıcı et al. A comparative study on denoising from facial images using convolutional autoencoder
CN117853850B (zh) 一种用于nk细胞培育过程中的检测评估系统和方法
CN112101377B (zh) 一种基于区域特征分析的在线间歇中空滤棒检测方法
CN112381136B (zh) 目标检测方法和装置
Jrad et al. A Novel Otsu Watershed based Method Applied for DNA Scalograms Segmentation
CN107590798B (zh) 一种生物组织三维图像背景去除系统和方法
Dong et al. Image fog density recognition method based on multi-feature model and S-DAGSVM

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 17879217

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 17879217

Country of ref document: EP

Kind code of ref document: A1