PT  - JOURNAL ARTICLE
AU  - Nathan E. Hall
AU  - Jared Mamrot
AU  - Christopher M.A. Frampton
AU  - Prue Read
AU  - Edward J. Steele
AU  - Robert J. Bischof
AU  - Robyn A. Lindley
TI  - Deaminase associated single nucleotide variants in blood and saliva-derived exomes from healthy subjects
AID  - 10.1101/807073
DP  - 2019 Jan 01
TA  - bioRxiv
PG  - 807073
4099  - http://biorxiv.org/content/early/2019/10/16/807073.short
4100  - http://biorxiv.org/content/early/2019/10/16/807073.full
AB  - Background Deaminases play an important role in shaping inherited and somatic variants. Disease related SNVs are associated with deaminase mutagenesis and genome instability. Here, we investigate the reproducibility and variance of whole exome SNV calls in blood and saliva of healthy subjects and analyze variants associated with AID, ADAR, APOBEC3G and APOBEC3B deaminase sequence motifs.Methods Samples from twenty-four healthy Caucasian volunteers, allocated into two groups, underwent whole exome sequencing. Group 1 (n=12) analysis involved one blood and four saliva replicates. A single saliva sample was sequenced for Group 2 subjects (n=12). Overall, a total of 72 whole exome datasets were analyzed. Biological (Group 1 & 2) and technical (Group 1) variance of SNV calls and deaminase metrics were calculated and analyzed using intraclass correlation coefficients. Candidate somatic SNVs were identified and evaluated.Results We report high blood-saliva concordance in germline SNVs from whole exome sequencing. Concordant SNVs, found in all subject replicates, accounted for 97% of SNVs located within the protein coding sequence of genes. Discordant SNVs have a 30% overlap with variants that fail gnomAD quality filters and are less likely to be found in dbSNP. SNV calls and deaminase-associated metrics were found to be reproducible and robust (intraclass correlation coefficients >0.95). No somatic SNVs were conclusively identified when comparing blood and saliva samples.Conclusions Saliva and blood both provide high quality sources of DNA for whole exome sequencing, with no difference in ability to resolve SNVs and deaminase-associated metrics. We did not identify somatic SNVs when comparing blood and saliva of healthy individuals, and we conclude that more specialized investigative methods are required to comprehensively assess the impact of deaminase activity on genome stability in healthy individuals.