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Article

CandiSNPer: a web tool for the identification of candidate SNPs for causal variants.

Bioinformatics (Oxford, England) - 1 Apr 2010

Schmitt Armin O, Assmus Jens, Bortfeldt Ralf H, Brockmann Gudrun A

Abstract excerpt

SUMMARY: Human single nucleotide polymorphism (SNP) chips which are used in genome-wide association studies (GWAS) permit the genotyping of up to 4 million SNPs simultaneously. To date, about 1000 human SNPs have been identified as statistically significantly associated with a disease or another...

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PMID: 20172942
DOI: 10.1093/bioinformatics/btq068

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20172942-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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