Nothing
Identification of the most likely gene or genes through which variation at a given genomic locus in the human genome acts. The most basic functionality assumes that the closer gene is to the input locus, the more likely the gene is to be causative. Additionally, any empirical data that links genomic regions to genes (e.g. eQTL or genome conformation data) can be used if it is supplied in the UCSC .BED file format.
Package details |
|
---|---|
Author | Arthur Wuster |
Bioconductor views | GenePrediction GenomeWideAssociation GenomicVariation SNP VariantAnnotation |
Maintainer | Arthur Wuster <wustera@gene.com> |
License | Artistic-2.0 |
Version | 1.16.0 |
Package repository | View on Bioconductor |
Installation |
Install the latest version of this package by entering the following in R:
|
Any scripts or data that you put into this service are public.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.