A total of 7.0 × 1015 bases of DNA-sequencing data were generated, consisting of an average of 129.6 × 109 bases of sequence distributed across 864.2 million paired reads (each 100–151 base pairs (bp) long) per individual. For a typical individual, 99.65% of the bases in the reference genome were covered, to a mean read depth of 38.2×.
