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Whole genome DNA sequencing statistics.
| Average reads uniquely aligned to human genome* | Average genome coverage | Average discordant SNP calls | Average discordant exonic/splicing SNP calls | Discordant SNP calls in NSCLP candidate genes |
| 9.19E + 10 (8.61E + 10–1.01E + 11) | 29.12 (28.42–32.52) | 196,253 (187,112–213,468) | 14,920 (13,435–19,423) | 0 (0–0) |
*Range in brackets.
