Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor is a research paper published in Bioinformatics (2010). On theSindex it has a DataRank of 21.5. It has been cited 1,669 times, with 200 citing works in its 1-hop citation network.
Scored on demand from live citation data
DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?
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Base Score Contribution
1.1
From this paper's citation signal
Citation Network Contribution
20.4
From 200 citing papers with measurable signal
Wellcome Trust
Grant: unidentified
unidentified
European Commission
Grant: 200754
Genotype-To-Phenotype Databases: A Holistic Solution
Wellcome Trust
FWCI
18.93
Citation Percentile
1.0%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals