Bioinformatics Advance Access published online on February 21, 2006
Bioinformatics, doi:10.1093/bioinformatics/btl042
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1 Windber Research Institute, Windber, PA 15963
* To whom correspondence should be addressed.
Motivation: Pathway modeling requires the integration of multiple data including prior knowledge. In this study, we quantitatively assess the application of Gene Ontology (GO)-derived similarity measures for the characterization of direct and indirect interactions within human regulatory pathways. The characterization would help the integration of prior pathway knowledge for the modeling. Results: Our analysis indicates information content-based measures outperform graph structure-based measures for stratifying protein interactions. Measures in terms of GO biological process and molecular function annotations can be used alone or together for the validation of protein interactions involved in the pathways. However, GO cellular component-derived measures may not have the ability to separate true positives from noise. Furthermore, we demonstrate that the functional similarity of proteins within known regulatory pathways decays rapidly as the path length between two proteins increases. Several logistic regression models are built to estimate the confidence of both direct and indirect interactions within a pathway, which may be used to score putative pathways inferred from a scaffold of molecular interactions.
Received September 20, 2005
Revised January 16, 2006
Accepted February 3, 2006
Article
Assessing semantic similarity measures for the characterization of human regulatory pathways
Xiang Guo 1 *,
Rongxiang Liu 2,
Craig D. Shriver 3,
Hai Hu 1,
and
Michael N. Liebman 1
2 GlaxoSmithKline Pharmaceutical R&D, King of Prussia, PA 19420
3 Walter Reed Army Medical Center, Washington, DC 20307
Xiang Guo, E-mail: s.guo{at}wriwindber.org
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Abstract
Associate Editor: Chris Stoeckert
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