SNiPA: an interactive, genetic variant-centered annotation browser.
Where this comes from
- Record sourced from PubMed, PMID 25431330.
- Also identified by DOI 10.1093/bioinformatics/btu779 and PMC identifier 4393511.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Linking genes and functional information to genetic variants identified by association studies remains difficult. Resources containing extensive genomic annotations are available but often not fully utilized due to heterogeneous data formats. To enhance their accessibility, we integrated many annotation datasets into a user-friendly webserver. http://www.snipa.org/ g.kastenmueller@helmholtz-muenchen.de Supplementary data are available at Bioinformatics online.
Medical subject headings
- Databases, Genetic
- Genetic Variation
- Genome, Human
- Genomics
- Molecular Sequence Annotation
- Software