Journal
BIOINFORMATICS
Volume 24, Issue 3, Pages 440-442Publisher
OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btm587
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Funding
- NCI NIH HHS [5 U54 CA121852-03] Funding Source: Medline
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We present MutaGeneSys: a system that uses genome-wide genotype data to estimate disease susceptibility. Our system integrates three data sources: the International HapMap project, whole-genome marker correlation data and the Online Mendelian Inheritance in Man (OMIM) database. It accepts SNP data of individuals as query input and delivers disease susceptibility hypotheses even if the original set of typed SNPs is incomplete. Our system is scalable and flexible: it produces population, technology and confidence-specific predictions in interactive time.
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