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Annotation of Genetic Variants

Results 27 VariantAnnotation issues
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The majority of VCF handling bioinformatics libraries use a `.vcf.gz` suffix, even for block gziped output. `writeVcf()` with `index=TRUE` does not support this and forceably sets the suffix to `.bgz`....

enhancement

Hi , I'm the creator of the MungeSumstats Bioconductor package in which we use VariantAnnotation::writeVcf as an output options for the formatted sumstats. I want to align the formatting of...

It would be nice to have an efficient utility to merge two VCF objects that have differing (but often overlapping) sets of variants and samples. I guess the assay matrices...

Hello, I'm looking at an intergenic variant (in the bovine genome) and want to figure the genes relative to which it is downstream or upstream, i.e. relative to the gene's...

As the title indicates, I have to add "which=rowRanges()" to make the `readVcfStack` work when using `param`. `readVcf` works as expected. Issue only exist in Bioc devel. Coding in bioc...

Dear BiocTeam, I am investigating the proteome of human cancer samples and want to insert their genetic variations into the reference proteome fasta sequences to increase the sensitivity of my...

I have HIV sequence data, where for three consecutive positions I have SNPS. These three all code for SNPS in the same codon. predictcoding() returns the independently evaluated REFAA and...

Hello VariantAnnotation team, I am using the predictCoding function to annotate the coding consequence of SNPs in my VCF file using a custom GTF file. Here is what I ran:...

Minimal example: ```r library(VariantAnnotation) fl