StructuralVariantAnnotation contains useful helper functions for dealing with structural variants in VCF format. The packages contains functions for parsing VCFs from a number of popular callers as well as functions for dealing with breakpoints involving two separate genomic loci encoded as GRanges objects.
|Bioconductor views||Annotation DataImport Genetics Sequencing VariantAnnotation|
|Package repository||View on GitHub|
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