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VCF files describing the known mutations in each read file

dataset
posted on 2012-07-16, 15:43 authored by Gavin Oliver

VCF files describing the mutations contained in the sixty-seven groups of BRCA1 reads. These were selected from a test set of 2211 (1299 unique) known BRCA1 variants containing 1340 SNPs, 320 insertions and 551 deletions.

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