Skip to main content
Fig. 5 | Genome Biology

Fig. 5

From: Systematic comparative analysis of single-nucleotide variant detection methods from single-cell RNA sequencing data

Fig. 5

The performance measurements of variant-calling tools with different variant allele frequencies in simulated data. a The flowchart showing the simulation procedure of inserting random variants to mapped BAM file and the performance assessments based on simulation. b–d Boxplots showing the F-scores (b), TPRs (c), and FDRs (d) with minimal read depths ≥ 10 at SNP loci in high-confidence coding regions. e–g Boxplots showing the F-scores (e), TPRs (f), and FDRs (g) with minimal supporting reads for the variant ≥ 10 in high-confidence coding regions

Back to article page