categorize.variants | R Documentation |
This function intersects the given variants with the genes in that region and classifies them according to "intergenic", "3UTR", "exon", "intron" or "5UTR".
categorize.variants(variants,
mgi.file = "http://cgd.jax.org/tools/SNPtools/MGI/MGI.20130305.sorted.txt.gz")
variants |
data.frame, Variants as returned by |
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". |
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.
Daniel Gatti
get.variants{get.variants}
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