Fig. 5
From: Quality of whole genome sequencing from blood versus saliva derived DNA in cardiac patients
Proportion of rare single nucleotide variants (MAF < 1% in general population) in saliva genomes (n = 5). The bar graph shows average proportion of all rare SNVs called in blood genomes that were also detected in a paired saliva sample genome-wide, in CCDS transcripts, and in CVD gene transcripts
