\documentclass[11pt]{article} \setlength{\oddsidemargin}{0.0truein} \setlength{\evensidemargin}{0.0truein} \setlength{\textwidth}{6.5truein} \setlength{\topmargin}{0.0truein} \setlength{\textheight}{9.0truein} \setlength{\headsep}{0.0truein} \setlength{\headheight}{0.0truein} \setlength{\topskip}{10.0pt} \setlength{\parskip}{5mm} \usepackage{url} \begin{document} \begin{center} \textbf{\textsc{STANFORD UNIVERSITY}}\\[5pt] \textbf{\textsc{DEPARTMENT OF STATISTICS}}\\[5pt] \Large{\textbf\textsc{{DEPARTMENTAL SEMINAR}}} \end{center} \begin{center} 4:15 p.m., Tuesday, April 11, 2006\\ Sequoia Hall Room 200\\ (Cookies at 3:45 in 1st Floor Lounge) \end{center} \begin{center} \textsl{Balaji S. Srinivasan}\\ Depts. of Electrical Engineering \& Developmental Biology \\ Stanford University \end{center} \begin{center} \large \textbf{Network Integration Reveals Hidden Biology in 230 Microbes} \normalsize \end{center} \noindent We have combined four different kinds of functional genomic data to create high coverage, probabilistic protein interaction networks for 230 microbes. Our integration algorithm naturally handles statistically dependent predictors and automatically corrects for differing noise levels and data corruption in different evidence sources. We find that a plurality of the predictions in each integrated network hinge on moderate but consistent evidence from multiple sources rather than strong evidence from a single source, yielding novel biology that would be missed if a single data source such as coexpression or coinheritance were used in isolation. \noindent We demonstrate that these hidden interactions uncover new aspects of well studied functional modules in a broad range of microbial species. We accompany this analysis with a strategy for systematic, computer-guided laboratory validation and present experimental verification of our predictions in \textit{Caulobacter crescentus}. \noindent As our work represents the largest collection of probabilistic protein interaction networks compiled to date, we have created tools for network alignment to organize this information. By developing the first scalable multiple network alignment algorithm, we have identified thousands of conserved modules in diverse microbial species. Our integration, validation, and alignment algorithms can be applied to any sequenced organism and any kind of experimental or computational technique which produces pairwise measures of protein interaction. \noindent Short Biography: \noindent Balaji Srinivasan received his bachelor's degree in Electrical Engineering and master's degrees in Chemical Engineering and Electrical Engineering from Stanford University. He is currently a PhD student in Electrical Engineering scheduled to defend on April 28, 2006. In July 2006 he will be joining the Statistics department as a VIGRE postdoctoral fellow in the area of computational biology. His research interests include systems biology, population genetics, and data mining. His work on network integration received the best poster award at the 2005 Cold Spring Harbor Genome Informatics conference. \end{document}