categorize.variants: categorize.variants

Description Usage Arguments Value Author(s) See Also

Description

This function intersects the given variants with the genes in that region and classifies them according to "intergenic", "3UTR", "exon", "intron" or "5UTR".

Usage

1
2
 categorize.variants(variants, 
        mgi.file = "http://cgd.jax.org/tools/SNPtools/MGI/MGI.20130305.sorted.txt.gz") 

Arguments

variants

data.frame, Variants as returned by get.variants{get.variants}.

mgi.file

Character, full path to the MGI feature file. On the JAX campus, this defaults to "http://cgd.jax.org/tools/SNPtools/MGI/MGI.20130305.sorted.txt.gz".

Value

FALSEor SNPs and Indels: data.frame: with eight columns: ID, CHR, POS, REFALSE, ALT, symbol, id, type. The first four columns are simply copied over from the SNP file. The symbol column contains the Gene Symbol. The id column contains a gene ID (MGI, Ensembl, NCBI or VEGA). The type column contains "intergenic", "3UTR", "exon", "intron" or "5UTR", depending on the location of the variant in a gene. FALSEor SVs: data.frame: with eight columns: ID, CHR, POS, REFALSE, ALT, symbol, id, type. The first four columns are simply copied over from the SNP file. The symbol column contains the Gene Symbol. The id column contains a gene ID (MGI, Ensembl, NCBI or VEGA). The type column contains "intergenic", "3UTR", "exon", "intron" or "5UTR", depending on the location of the variant in a gene.

Author(s)

Daniel Gatti

See Also

get.variants{get.variants}


DOQTL documentation built on May 6, 2019, 3:09 a.m.