Align human interactome with phenome to identify causative genes and networks underlying disease families

Motivation: Understanding the complexity in gene–phenotype relationship is vital for revealing the genetic basis of common diseases. Recent studies on the basis of human interactome and phenome not only uncovers prevalent phenotypic overlap and genetic overlap between diseases, but also reveals a mo...

Full description

Saved in:
Bibliographic Details
Published inBioinformatics Vol. 25; no. 1; pp. 98 - 104
Main Authors Wu, Xuebing, Liu, Qifang, Jiang, Rui
Format Journal Article
LanguageEnglish
Published Oxford Oxford University Press 01.01.2009
Oxford Publishing Limited (England)
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Motivation: Understanding the complexity in gene–phenotype relationship is vital for revealing the genetic basis of common diseases. Recent studies on the basis of human interactome and phenome not only uncovers prevalent phenotypic overlap and genetic overlap between diseases, but also reveals a modular organization of the genetic landscape of human diseases, providing new opportunities to reduce the complexity in dissecting the gene–phenotype association. Results: We provide systematic and quantitative evidence that phenotypic overlap implies genetic overlap. With these results, we perform the first heterogeneous alignment of human interactome and phenome via a network alignment technique and identify 39 disease families with corresponding causative gene networks. Finally, we propose AlignPI, an alignment-based framework to predict disease genes, and identify plausible candidates for 70 diseases. Our method scales well to the whole genome, as demonstrated by prioritizing 6154 genes across 37 chromosome regions for Crohn's disease (CD). Results are consistent with a recent meta-analysis of genome-wide association studies for CD. Availability: Bi-modules and disease gene predictions are freely available at the URL http://bioinfo.au.tsinghua.edu.cn/alignpi/ Contact: ruijiang@tsinghua.edu.cn Supplementary information: Supplementary data are available at Bioinformatics online.
Bibliography:istex:769C6C82333DDBA7677F8A26BA5A5EF0BEA619F9
To whom correspondence should be addressed.
Associate Editor: Trey Ideker
ark:/67375/HXZ-HLLXW7DF-6
ArticleID:btn593
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1367-4803
1460-2059
1367-4811
DOI:10.1093/bioinformatics/btn593