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Volume 90, Issue 4, Pages 225-235 (July 2010)


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TB database 2010: Overview and update

James E. GalaganabcCorresponding Author Informationemail address, Peter Siska, Christian Stoltea, Brian Weinera, Michael Koehrsena, Farrell Wymored, T.B.K. Reddyd, Jeremy D. Zuckera, Reinhard Engelsa, Marcel Gellescha, Jeremy Hubblee, Heng Jind, Lisa Larsona, Maria Maoe, Michael Nitzbergd, Jared Whitea, Zachariah K. Zachariahd, Gavin Sherlocke, Catherine A. Balld, Gary K. Schoolnikf

Received 15 March 2010; accepted 31 March 2010. published online 21 May 2010.

Summary 

The Tuberculosis Database (TBDB) is an online database providing integrated access to genome sequence, expression data and literature curation for TB. TBDB currently houses genome assemblies for numerous strains of Mycobacterium tuberculosis (MTB) as well assemblies for over 20 strains related to MTB and useful for comparative analysis. TBDB stores pre- and post-publication gene-expression data from M. tuberculosis and its close relatives, including over 3000 MTB microarrays, 95 RT-PCR datasets, 2700 microarrays for human and mouse TB related experiments, and 260 arrays for Streptomyces coelicolor. To enable wide use of these data, TBDB provides a suite of tools for searching, browsing, analyzing, and downloading the data. We provide here an overview of TBDB focusing on recent data releases and enhancements. In particular, we describe the recent release of a Global Genetic Diversity dataset for TB, support for short-read re-sequencing data, new tools for exploring gene expression data in the context of gene regulation, and the integration of a metabolic network reconstruction and BioCyc with TBDB. By integrating a wide range of genomic data with tools for their use, TBDB is a unique platform for both basic science research in TB, as well as research into the discovery and development of TB drugs, vaccines and biomarkers.

a Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA

b Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA

c National Emerging Infectious Diseases Lab, Boston University, Boston MA 02118, USA

d Department of Biochemistry, Stanford University School of Medicine, Stanford, CA 94305, USA

e Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305-5120, USA

f Department of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA

Corresponding Author InformationCorresponding author. Department of Biomedical Engineering, Boston University, 24 Cummington Street, Boston, MA 02215, USA. Tel.: +1 617 875 9874.

PII: S1472-9792(10)00041-7

doi:10.1016/j.tube.2010.03.010


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