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ASSIMILATOR: a new tool to inform selection of associated genetic variants for functional studies

Paul Martin; Anne Barton; Stephen Eyre

Bioinformatics. 2011;27(1):144-146.

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Abstract

Motivation: Fine-mapping experiments from genome-wide association studies (GWAS) are underway for many complex diseases. These are likely to identify a number of putative causal variants, which cannot be separated further in terms of strength of genetic association due to linkage disequilibrium. The challenge will be selecting which variant to prioritize for subsequent expensive functional studies. A wealth of functional information generated from wet lab experiments now exists but cannot be easily interrogated by the user. Here, we describe a program designed to quickly assimilate this data called ASSIMILATOR and validate the method by interrogating two regions to show its effectiveness.

Bibliographic metadata

Type of resource:
Content type:
Publication type:
Publication form:
Published date:
Journal title:
Volume:
27
Issue:
1
Start page:
144
End page:
146
Digital Object Identifier:
10.1093/bioinformatics/btq611
Access state:
Active

Institutional metadata

University researcher(s):

Record metadata

Manchester eScholar ID:
uk-ac-man-scw:101823
Created by:
Martin, Paul
Created:
23rd December, 2010, 12:10:44
Last modified by:
Martin, Paul
Last modified:
23rd August, 2012, 20:25:42

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