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Article

M(3)-S: a genotype calling method incorporating information from samples with known genotypes.

BMC bioinformatics - 3 Dec 2015

Li Gengxin, Zhao Hongyu

Abstract excerpt

BACKGROUND: A key challenge in analyzing high throughput Single Nucleotide Polymorphism (SNP) arrays is the accurate inference of genotypes for SNPs with low minor allele frequencies. A number of calling algorithms have been developed to infer genotypes for common SNPs, but they are limited in their performance in calling rare SNPs. The existing algorithms can be broadly classified into three categories,...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 26634345
DOI: 10.1186/s12859-015-0824-5
PMCID: PMC4669649

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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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