Journal
BIOINFORMATICS
Volume 26, Issue 16, Pages 2069-2070Publisher
OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btq330
Keywords
-
Categories
Funding
- Wellcome Trust
- European Community [200754]
Ask authors/readers for more resources
A tool to predict the effect that newly discovered genomic variants have on known transcripts is indispensible in prioritizing and categorizing such variants. In Ensembl, a web-based tool (the SNP Effect Predictor) and API interface can now functionally annotate variants in all Ensembl and Ensembl Genomes supported species.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available