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. 2022 Jan 15;25(2):103777. doi: 10.1016/j.isci.2022.103777

Figure 1.

Figure 1

scRNA-seq gene body coverage skewness and skewness distribution

Three scRNA-seq datasets.

(A) Distribution of mapped reads (tags) across genes. Each panel shows the gene body coverage percentile per dataset. The x axis represents the gene body from 5′ end to 3′ end scaled from 0 to 100, and the y axis denotes gene coverage (0–1). lThe plot of the dataset (ArrayExpress: E-MTAB-2600) generated by SMARTer protocol (full-length sequence) contains cells with low coverage in the middle of the gene region and cells with high coverage in the 3′ -end of the gene region. Although the dataset (NCBI GEO:GSE29087) generated by STRT (5′ -end sequence) contains cells with high coverage both in the middle and the 3′ -end region of the gene. The third dataset from 10x Genomics generated by single-cell 3′ -end protocol contains cells with high coverage in the 5′ -end region of the gene and cells with low coverage in the middle of the gene.

(B) Mean of the gene body coverage for different scRNA-seq methods. Error bars represents the standard error of the mean (SEM).

(C) Skewness and bias in gene body coverage for cells highlighted with a red dashed box.