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Article

Significance of functional disease-causal/susceptible variants identified by whole-genome analyses for the understanding of human diseases.

Proceedings of the Japan Academy. Series B, Physical and biological sciences - 1 Jan 2017

Hitomi Yuki, Tokunaga Katsushi

Abstract excerpt

Human genome variation may cause differences in traits and disease risks. Disease-causal/susceptible genes and variants for both common and rare diseases can be detected by comprehensive whole-genome analyses, such as whole-genome sequencing (WGS), using next-generation sequencing (NGS) technology and genome-wide association studies (GWAS). Here, in addition to the application of an NGS as a whole-genome analysis...

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Identifiers

PMID: 29129848
DOI: 10.2183/pjab.93.042
PMCID: PMC5743846

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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