mapRecomb | R Documentation |
This function takes as an input phased VCF files for each member of a family trio and maps breakpoints of meiotic recombination in each inherited parental homolog.
mapRecomb(
parent1 = NULL,
parent2 = NULL,
child = NULL,
genome = "hg38",
method = "CBS",
minSeg = 100,
smooth = 3,
collapse.amb = TRUE
)
parent1 |
A path to a VCF file to be loaded for a parent 1. |
parent2 |
A path to a VCF file to be loaded for a parent 2. |
child |
A path to a VCF file to be loaded for a child. |
genome |
A reference genome used by readVcfAsVRanges function. [e.g. 'hg38' - human] |
method |
A user defined method to be used to map changes in haplotype blocks [default: CBS] |
minSeg |
Minimal length (number of variants) being reported as haplotype block ( |
smooth |
Number of consecutive variants being considered as a random error and so being corrected (flipped). |
collapse.amb |
Set to |
A list
object that contains mapped meiotic breakpoints and inherited hapltype segments
for each homolog in a child.
David Porubsky
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