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Research Labs

The Butte Lab

Lab Overview

Translational bioinformatics has been defined as the development of analytic, storage, and interpretive methods to optimize the transformation of increasingly voluminous genomic and biological data into diagnostics and therapeutics for the clinician.

The long-term research goal of the Butte Lab is to develop translational bioinformatics methods to reason over many available genome-scale measurement and experimental modalities, and apply these methods to study complex disorders in genomic medicine, especially obesity and type 2 diabetes mellitus.

The Butte Lab has three main directions in exploring translational bioinformatics. First, we have developed bioinformatics methods to integrate genomic, genetic, phenotypic, clinical, and gene-knockout data from multiple sources and phenotypes and reason over these data. An example of this was our recent work on fat cell formation published in Nature Cell Biology (2005) and on obesity in Bioinformatics (2007, in press). Second, we have developed tools to automatically index and find genomic and proteomic data sets based on the phenotypic and contextual details of each experiment. We used these tools to create a comprehensive phenome-genome network published in Nature Biotechnology (2006). Third, we are building a novel gene-expression-based classification scheme for diseases across the entire field of medicine. Initial work on this will appear in Nature Methods (2007, in press).

Related People

Sanchita Bhattacharya
Sr. Bioinformatics Research Specialist
Atul J. Butte, M.D., Ph.D.
Assistant Professor of Medicine (Biomedical Informatics) and Pediatrics
Rong Chen, Ph.D.
Staff Bioinformatics Programmer
Annie P. Chiang, Ph.D.
Postdoctoral Research Fellow
Joel Dudley
Staff Bioinformatics Programmer
Keiichi Kodama, MD, PhD
Postdoctoral Research Fellow
Shivkumar Venkatasubrahmanyam, Ph.D.
Postdoctoral Research Fellow

Related Publications Only the 5 most recent displayed

BMIR-2009-1362
Identifying compartment-specific non-HLA targets after renal transplantation by integrating transcriptome and ‘‘antibodyome’’ measures
L. Li, P. Wadia, M. Sarwal, N. Kambham, T. Sigdel, D. B. Miklos, R. Chen, M. Naesens, A. J. Butte
PNAS, 106, 11, 4148-4153. Published in 2009
BMIR-2008-1353
GeneChaser: Identifying all biological and clinical conditions in which genes of interest are differentially expressed
R. Chen, R. Mallelwar, A. Thosar, S. Venkatasubrahmanyam, A. J. Butte
BMC Bioinformatics, 9, 1, 548. (doi:10.1186/1471-2105-9-548). Published in 2008
BMIR-2008-1346
FitSNPs: highly differentially expressed genes are more likely to have variants associated with disease
R. Chen, A. A. Morgan, J. Dudley, A. M. Deshpande, L. Li, K. Kodama, A. P. Chiang, A. J. Butte
Genome Biology, 9, 12, R170 (doi:10.1186/gb-2008-9-12-r170). Published in 2008
BMIR-2008-1338
Using SNOMED-CT For Translational Genomics Data Integration
J. Dudley, D. P. Chen, A. J. Butte
Ronald Cornet, Kent Spackman (eds.): Representing and sharing knowledge using SNOMED. Proceedings of the 3rd International Conference on Knowledge Rep, Pheonix (AZ), USA, CEUR Workshop Proceedings, ISSN 1613-0073, online CEUR-WS.org/Vol-410/, 91-96. Published in 2008
BMIR-2008-1303
The Ultimate Model Organism
A. J. Butte
Science, 320, 5874, 325-327. Published in 2008

Projects

AILUN
View Project
Diabetes and Obesity Integrative Genomics
View Project
fitSNP
View Project
GENECHASER
View Project
Genomic Nosology for Medicine (GNOMED)
View Project
Genotext
View Project
Relevance Networks
View Project

Related Events

BMIR Faculty External Invited Seminar
Atul Butte speaking at the Van Andel Research Institute
Date:
Wed, Oct 3 2007
Location:
Van Andel Research Institute, Grand Rapids, Michigan
Speaker:
Atul Butte
Project:
Genomic Nosology for Medicine (GNOMED)
Affiliation:
Stanford University

Stanford School of Medicine