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High-throughput single-cell transcriptome and gene mutation integrated analysis integrated device

An integrated analysis and single-cell technology, applied in biochemical cleaning devices, enzymology/microbiology devices, bioreactor/fermenter combinations, etc. Problems such as high cost to achieve the optimization of treatment plan and optimization of new target discovery

Active Publication Date: 2022-05-20
SUZHOU INST OF BIOMEDICAL ENG & TECH CHINESE ACADEMY OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the three-generation sequencing technology used in this study to detect mutations has great limitations. The mutation detection rate is limited by the specific mutation site. The highest single mutation detection rate is only 23%, and the average number of cells that can detect mutations does not exceed 5%, the author finally used the random forest machine learning algorithm to predict the tumor population, which could not realize the direct identification of the tumor cell population, and did not correspond well to the heterogeneity of the genome and transcriptome
Moreover, the technique is cumbersome to operate, requires a high sample volume, and costs a lot, making it unsuitable for general promotion.

Method used

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  • High-throughput single-cell transcriptome and gene mutation integrated analysis integrated device
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  • High-throughput single-cell transcriptome and gene mutation integrated analysis integrated device

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0055] Based on the above, a specific integrated analysis device 2 is provided in this embodiment.

[0056] refer to Figure 2-8 , wherein the light source assembly 6 includes a first LED light source 60, a second LED light source 61, a third LED light source 62, a first dichroic mirror 63, a second dichroic mirror 64 and a beam expander lens group 65, the first LED The light emitted by the light source 60 is transmitted through the first dichroic mirror 63 and the second dichroic mirror 64 in turn and reaches the beam expander lens group 65; the light emitted by the second LED light source 61 is reflected by the first dichroic mirror 63, and the second dichroic mirror The dichroic mirror 64 transmits and reaches the beam expander lens group 65; the light emitted by the third LED light source 62 reaches the beam expander lens group 65 after being reflected by the second dichroic mirror 64; the first LED light source 60, the second LED light source 61 , The third LED light sou...

Embodiment 2

[0063] Based on the above, a high-throughput single-cell encoding chip 1 is provided.

[0064] Among them, the chip is provided with a plurality of microwells on its substrate, each microwell has a unique spatial coordinate code, and several known nucleic acid sequences for capturing target RNA are modified in the microwells, and the nucleic acid sequences include A cell label indicating the cell from which the RNA originated and a molecular label used to identify the bound RNA, the cell label of each microwell corresponds to the spatial coordinate code one-to-one.

[0065] Wherein, the nucleic acid sequence also includes a Spacer sequence, a universal primer sequence as a primer binding region during PCR amplification, and Ploy T. In a further preferred embodiment, the modified nucleic acid sequence in each microwell is not less than 10 6 strip. A molecular tag is a known random nucleic acid sequence.

[0066] Here, the microwells have a size and shape that can accommodate...

Embodiment 3

[0077] An integrated high-throughput single-cell transcriptome and gene mutation integrated analysis device is provided, which is obtained by combining the integrated analysis device 2 of Example 1 and the high-throughput single-cell coding chip 1 of Example 2.

[0078] The analysis steps of the high-throughput single-cell transcriptome and gene mutation integrated analysis integrated device in this embodiment include:

[0079] 1) Fluorescently label the target gene of the cells in advance, then add the sample to the high-throughput single-cell coding chip 1, capture single cells through the micropores on it, and place the high-throughput single-cell coding chip 1 on the loading heat On stage 40, light source assembly 6, microscope objective lens 7, fluorescence spectroscopic assembly 8, and imaging detector 9 are activated, and fluorescence imaging is performed on high-throughput single-cell encoding chip 1 through fluorescence imaging module 5, and then the data storage and a...

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Abstract

The invention discloses a high-throughput single-cell transcriptome and gene mutation integrated analysis integrated device, which includes a high-throughput single-cell coding chip and an integrated analysis device; the integrated analysis device includes a casing and is arranged in the casing A temperature-controlled thermal cycle module, a fluorescence imaging module, and a data storage and analysis module, the fluorescence imaging module includes a light source assembly, a microscope objective lens, a fluorescence spectroscopic assembly, and an imaging detector. In the present invention, by designing a high-throughput single-cell coding chip with triple coding functions of micropore spatial coordinates, cellular nucleic acid tags, and molecular nucleic acid tags, the gene mutation, transcriptome, and protein expression information of single cells can be matched one by one; PCR amplification can be realized through the temperature-controlled thermal cycle module, the fluorescence image of the sample can be collected through the fluorescence imaging module, and the fluorescence image can be stored and analyzed through the data storage and analysis module, which can realize the integrated analysis of single-cell transcriptome and gene mutation.

Description

technical field [0001] The invention relates to the field of biological detection, in particular to a high-throughput single-cell transcriptome and gene mutation integrated analysis integrated device. Background technique [0002] Tumor is one of the major diseases that seriously affect human health. There are great differences in tumor cells from genotype to phenotype (high heterogeneity of tumors), and this high heterogeneity is related to the degree of malignancy and drug resistance of tumors. Sex, recurrence and metastasis are closely related, which is one of the root causes of difficult early diagnosis of tumors, complicated clinical diagnosis and treatment, drug-resistant recurrence and poor prognosis. A comprehensive analysis of tumor heterogeneity is the key to precise tumor treatment. [0003] The development of high-throughput sequencing technology brings hope for the analysis of heterogeneous tumor populations. At present, conventional high-throughput sequencing...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12M1/00C12M1/38C12M1/34C12Q1/6858
CPCC12Q1/6858C12Q2531/113C12Q2563/107C12Q2565/631
Inventor 周连群张芷齐姚佳李金泽李敏李传宇唐玉国李超张威郭振
Owner SUZHOU INST OF BIOMEDICAL ENG & TECH CHINESE ACADEMY OF SCI
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