highly significantp < 0.001
SNP Numbers, Coverage, and Correlations The mean number of sequencing reads (mean ± 1 S.D.) generated per individual from tissue samples (1,608,863 ± 307,130) was 2.1× more than the number of reads generated from swab samples (518,985 ± 238,072), and this was a highly significant difference ( Table S2 ; t = 9.693, p < 0.001).