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Article

Computational identification of candidate loci for recessively inherited mutation using high-throughput SNP arrays.

Bioinformatics (Oxford, England) - 1 Aug 2007

Laakso Marko, Tuupanen Sari, Karhu Auli, Lehtonen Rainer, Aaltonen Lauri A, Hautaniemi Sampsa

Abstract excerpt

MOTIVATION: Single nucleic polymorphisms (SNPs) are one of the most abundant genetic variations in the human genome. Recently, several platforms for high-throughput SNP analysis have become available, capable of measuring thousands of SNPs across the genome. Tools for analysing and visualizing these large genetic data sets in biologically relevant manner are rare. This hinders effective use of the SNP-array data...

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PMID: 17510170
DOI: 10.1093/bioinformatics/btm263

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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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