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Table 1 Basic sequencing statistics

From: Cancer of the ampulla of Vater: analysis of the whole genome sequence exposes a potential therapeutic vulnerability

Genome Number of uniquely mapping 50 bp reads Number of uniquely mapping bases Genome coverage Number of germline variants Uniquely mapping tag pairs Read-pair coverage
Germline 2,383,981,557 108,322,420,859 40 2,771,201 887,285,914 443
Tumor 2,215,368,333 100,400,536,852 37 - 863,886,211 432
  1. Read pair coverage = (Number of uniquely mappable tag-pairs) × (Insertlength)/Haploid genome size.