autosomalRecessiveHeterozygous | R Documentation |
This function aims to analyze the variants of the unaffected individuals, storing and grouping the heterozygous ones by gene. The affected individuals ought present two or more different heterozygous changes in the gene, and at least one of them shall come from each parent.
## S4 method for signature 'VariantFilteringParam'
autosomalRecessiveHeterozygous(param,
svparam=ScanVcfParam(),
BPPARAM=bpparam("SerialParam"))
param |
A |
svparam |
An instance of a |
BPPARAM |
An object of class |
This function requires as an input a VariantFilteringParam
class object built from an input multisample VCF file, along with a PED file.
An object of class VariantFilteringResults
including functional annotations on all selected variants.
Dei M. Elurbe and R. Castelo
Elurbe D.M., Mila, M., Castelo, R. The VariantFiltering package, in preparation.
autosomalRecessiveHomozygous
autosomalDominant
xLinked
deNovo
VariantFilteringResults
## Not run:
CEUvcf <- file.path(system.file("extdata", package="VariantFiltering"), "CEUtrio.vcf.bgz")
CEUped <- file.path(system.file("extdata", package="VariantFiltering"), "CEUtrio.ped")
param <- VariantFilteringParam(vcfFilename=CEUvcf,
pedFilename=CEUped)
reHet <- autosomalRecessiveHeterozygous(param)
reHet
## End(Not run)
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