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Article

DIVAN: accurate identification of non-coding disease-specific risk variants using multi-omics profiles.

Genome biology - 6 Dec 2016

Chen Li, Jin Peng, Qin Zhaohui S

Abstract excerpt

Understanding the link between non-coding sequence variants, identified in genome-wide association studies, and the pathophysiology of complex diseases remains challenging due to a lack of annotations in non-coding regions. To overcome this, we developed DIVAN, a novel feature selection and ensemble learning framework, which identifies disease-specific risk variants by leveraging a comprehensive collection of...

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Identifiers

PMID: 27923386
DOI: 10.1186/s13059-016-1112-z
PMCID: PMC5139035

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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