PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations

SUMMARY: PhenoScanner is a curated database of publicly available results from large-scale genetic association studies in humans. This online tool facilitates ‘phenome scans’, where genetic variants are cross-referenced for association with many phenotypes of different types. Here we present a major...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Bioinformatics
Egile Nagusiak: Kamat, Mihir A, Blackshaw, James A, Young, Robin, Surendran, Praveen, Burgess, Stephen, Danesh, John, Butterworth, Adam S, Staley, James R
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2019
Gaiak:
Applications Notes
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6853652/
https://ncbi.nlm.nih.gov/pubmed/31233103
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btz469
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