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Article

SEQMINER: An R-Package to Facilitate the Functional Interpretation of Sequence-Based Associations.

Genetic epidemiology - 1 Dec 2015

Zhan Xiaowei, Liu Dajiang J

Abstract excerpt

Next-generation sequencing has enabled the study of a comprehensive catalogue of genetic variants for their impact on various complex diseases. Numerous consortia studies of complex traits have publically released their summary association statistics, which have become an invaluable resource for learning the underlying biology, understanding the genetic architecture, and guiding clinical translations. There is...

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Identifiers

PMID: 26394715
DOI: 10.1002/gepi.21918
PMCID: PMC4794281

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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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