Fig. 2
From: Accuracy benchmark of the GeneMind GenoLab M sequencing platform for WGS and WES analysis
Comparison of variants calling performances in GenoLab M and NovaSeq 6000 from 33X and 22X coverage of the NA12878 sample. A SNP and B InDel on whole genome, C SNP and D InDel F-score on stratification region. Precision, positive predictive value, is the fraction of relevant instances among the retrieved instances, Recall, sensitivity is the fraction of relevant instances that were retrieved. F-score is the harmonic mean of the precision and recall, chr 20 means chromosome 20, NIADR means Not in all Difficult Regions, SDR means Segmental Duplications Regions