Description Usage Arguments Value
quickly strips out the variants which are obviously nonfunctional
1 | remove_easy_nonfunctional(vars, vep)
|
vars |
seqminer::readVCFToListByRange output, list of values, which includes a genotype matrix as "GT", and sample IDs as sampleId. |
vep |
dataframe of VEP consequences for the vars entry |
dataframe of variants
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