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Article

RAINBOW: Haplotype-based genome-wide association study using a novel SNP-set method.

PLoS computational biology - 1 Feb 2020

Hamazaki Kosuke, Iwata Hiroyoshi

Abstract excerpt

Difficulty in detecting rare variants is one of the problems in conventional genome-wide association studies (GWAS). The problem is closely related to the complex gene compositions comprising multiple alleles, such as haplotypes. Several single nucleotide polymorphism (SNP) set approaches have been proposed to solve this problem. These methods, however, have been rarely discussed in connection with haplotypes. In...

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PMID: 32059004
DOI: 10.1371/journal.pcbi.1007663
PMCID: PMC7046296

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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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