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Chunk #9 — Results — Assay performance

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Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencing.
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in duplicate, obtaining more than 30 million pairs of reads per sample, resulting in approximately 24,000-fold coverage depth after mapping (Tables S3 and S4 in Additional file 2). Consistent with our previous report [13], the coverage distribution is uniform (82% of amplicons between 0.5- and 2-fold of the mean coverage) and reproducible between samples and across sequencing runs (Figure S3 in Additional file 1 and Table S4 in Additional file 2).