An ensemble approach to accurately detect somatic mutations using SomaticSeq
BSD 2-Clause "Simplified" License
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Could you provide documentation on the 70 features extracted by somaticseq? Trying to better understand SomaticSeq's model #48
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kiranchari closed 6 years ago
You can probably just look at this script https://github.com/bioinform/somaticseq/blob/master/SSeq_merged.vcf2tsv.py Starting line #137 is the part of the header whose features are being used. The same is also shown at the very end of the script. Most of the header names are pretty descriptive.