An S4 class containing the genomic location and allele information per sample for each variant from a VCF file.
Table
A data frame containing the genomic location and allele information per sample for each variant. It gives for each called variants the following information :
The chromosome of the variant)
The position of the variant
The reference sequence
The altered sequence
The quality of the variant call
The VCF filter of the variant call
The total reads count supporting the variant
The total reads count supporting the variant
The reads allele fraction
For each well samples
The total numbe rof reads covering the variant location at this smaple
Number of reads supporting the variant sequence at this smaple
Variant Reads allele fraction at this sample
colon separated list of unphased genotype at each sample
VariantAlleleInfo
, getVariantAlleleInfo
, getVariantCoverageTable
, plot.VariantAlleleInfo
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