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Chunk #35 — Online Methods — Virtual tumor benchmarking approach

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Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.
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The virtual tumor approach begins with deep-coverage data from a high coverage whole-genome sample (NA12878) sequenced on Illumina HiSeq instruments by the 1000 Genomes Project42 (2 libraries, “Solexa-18483” and “Solexa-18484”, at 30x each) and Gnerre et al.43 (1 library, “Solexa-23661”, at 30x). These data are publicly available – details are in Supplementary Table 5.