Additional file 1 of Quality of whole genome sequencing from blood versus saliva derived DNA in cardiac patients

Additional file 1: Table S1. Coordinates of all Consensus Coding Sequence (CCDS) transcripts in the hg19 genome build. Table S2. Coordinates of all cardiovascular disease (CVD) gene transcripts in the hg19 genome build. Table S3. Concordance of SNVs and CNVs between saliva and blood whole genomes. Table S4. Comparison of SNVs genome-wide in each paired blood and saliva genome. Table S5. Comparison of SNVs within CCDS transcripts in each paired blood and saliva genome. Table S6. Comparison of SNVs within CVD gene transcripts in each paired blood and saliva genome. Table S7. Comparison of rare SNVs genome-wide in each paired blood and saliva genome. Table S8. Comparison of rare SNVs within CCDS transcripts in each paired blood and saliva genome. Table S9. Comparison of rare SNVs within CVD gene transcripts in each paired blood and saliva genome. Table S10. Comparison of all CNVs genome-wide, within CCDS transcripts, and within CVD gene transcripts.