Cell subset annotation method based on single cell transcriptome sequencing
A technology of transcriptome sequencing and cell subgroups, which is applied in the field of bioinformatics analysis, can solve problems such as annotation of single cell subgroups, and achieve the effect of comprehensive cell subgroups and avoiding subjective consciousness
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Embodiment 1
[0037] Example 1 Cell Segmentation and Annotation of Normal Chorionic Cells
[0038] A cell subpopulation annotation method based on single-cell transcriptome sequencing, including the following steps:
[0039] S1. 10x barcode UMI identification: The off-machine sequencing data of the 10x genomics platform database is a fastq sequence, and the fastq sequence with the same ID number includes 3 parts: barcode+UMI+mRNA sequence, use the software cellrangercount to distinguish the sequence through the barcode sequence Source cells, quantify gene expression through UMI sequence, and use 3' end mRNA sequence for gene identification;
[0040] S2. Genome comparison: use the STAR algorithm to compare the fastq sequence obtained by sequencing to the reference genome, and locate the measured sequence to the corresponding gene;
[0041] S3. Gene expression profile construction: including the following steps: 1) Data integration and data volume normalization: when samples from multiple li...
Embodiment 2
[0052] Example 2 Cell Segmentation and Annotation of Diseased Chorionic Cells
[0053] A cell subpopulation annotation method based on single-cell transcriptome sequencing, including the following steps:
[0054] S1. 10x barcode UMI identification: The off-machine sequencing data of the 10x genomics platform database is a fastq sequence, and the fastq sequence with the same ID number includes 3 parts: barcode+UMI+mRNA sequence, use the software cellrangercount to distinguish the sequence through the barcode sequence Source cells, gene expression quantification by UMI sequence, gene identification by 3' end mRNA sequence;
[0055] S2. Genome comparison: use the STAR algorithm to compare the fastq sequence obtained by sequencing to the reference genome, and locate the measured sequence to the corresponding gene;
[0056] S3. Gene expression profile construction: including the following steps: 1) Data integration and data volume normalization: when samples from multiple librarie...
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