motifbreakR
MotifbreakR is a software tool designed to facilitate the functional annotation of germline and somatic variation revealed by genome-wide association studies (GWAS) and The Cancer Genome Atlas (TCGA). It allows users to assess the effects of variants on likely transcription factor binding sites and predict effects for novel or previously described variants in public databases. MotifbreakR is flexible and can be used to interrogate any genome curated within Bioconductor.
Topic
Sequence analysis;Nucleic acid sites, features and motifs;DNA polymorphism
Detail
Operation: Sequence motif analysis
Software interface: Command-line user interface;Library
Language: R
License: GNU General Public License, version 2
Cost: Free
Version name: 2.12.3
Credit: The National Institutes of Healthand National Cancer Institute.
Input: -
Output: -
Contact: Simon Gert Coetzee Simon.Coetzee@cshs.org
Collection: -
Maturity: Mature
Publications
- motifbreakR: an R/Bioconductor package for predicting variant effects at transcription factor binding sites.
- Coetzee SG, et al. motifbreakR: an R/Bioconductor package for predicting variant effects at transcription factor binding sites. motifbreakR: an R/Bioconductor package for predicting variant effects at transcription factor binding sites. 2015; 31:3847-9. doi: 10.1093/bioinformatics/btv470
- https://doi.org/10.1093/bioinformatics/btv470
- PMID: 26272984
- PMC: PMC4653394
Download and documentation
Source: http://bioconductor.org/packages/release/bioc/src/contrib/motifbreakR_2.12.3.tar.gz
Documentation: http://bioconductor.org/packages/release/bioc/manuals/motifbreakR/man/motifbreakR.pdf
Home page: http://bioconductor.org/packages/release/bioc/html/motifbreakR.html
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