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Article

wANNOVAR: annotating genetic variants for personal genomes via the web.

Journal of medical genetics - 1 Jul 2012

Chang Xiao, Wang Kai

Abstract excerpt

BACKGROUND: High-throughput DNA sequencing platforms have become widely available. As a result, personal genomes are increasingly being sequenced in research and clinical settings. However, the resulting massive amounts of variants data pose significant challenges to the average biologists and clinicians without bioinformatics skills. METHODS AND RESULTS: We developed a web server called wANNOVAR to address the...

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Identifiers

PMID: 22717648
DOI: 10.1136/jmedgenet-2012-100918
PMCID: PMC3556337

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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