Man pages for BartBroeckx/Mendelian
Variant Analysis for Mendelian Disorders

annotAnnotate variant data frame.
CLCfilePrepare CLC output for filtering
CLCfile1CLCfile1 documentation A dataset containing 8 variants...
CLCfile2CLCfile2 documentation A dataset containing 9 variants...
commonvarCombining the output of several filters.
gDomVariant filtering with dominant inheritance considering...
genBEDgenBED documentation A bed file containing genes used to...
gRecVariant filtering with recessive inheritance considering...
nDomVariant filtering with dominant inheritance
nRecVariant filtering with recessive inheritance
prepvarPreparing variant database.
prepvarparPreparing variant database (parallel).
SNPSNP documentation A dataset containing 472 variants from the...
testtest documentation An example of a VCF file.
varfilterFiltering variants from a database.
VCFfilePrepare VCF file for filtering.
BartBroeckx/Mendelian documentation built on May 28, 2017, 6:56 p.m.