View source: R/correctInversionPhasing.R
correctHomInv | R Documentation |
This function takes as an input region deemed to be a homozygous inversion and flips H1 and H2 haplotypes for SNVs that overlap with this region.
correctHomInv(correct.gr = NULL, vcf.file = NULL, ID = "")
correct.gr |
A |
vcf.file |
A StrandPhaseR formatted VCF file to be corrected for inversion phasing. |
ID |
A unique id to be appended at the end of each corrected VCF file. |
NULL
David Porubsky
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