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VCF files describing the known mutations in each read file
dataset
posted on 16.07.2012, 15:43 by Gavin OliverVCF 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.