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<strong>EMBL</strong>-EBI<br />

The Microarray Informatics Team<br />

Previous and current research<br />

The Microarray Informatics team is working in four main directions:<br />

• development of the ArrayExpress Archive and Atlas of Gene Expression;<br />

• high-throughput data integration and analysis;<br />

• development of algorithms for systems biology;<br />

• biomedical informatics-related research and development projects.<br />

Our group was among the first to use microarray data to study transcription regulation mechanisms<br />

on a genomic scale (Brazma et al., 1998). In 1999 we realised the importance of standards<br />

in microarray data reporting (Brazma et al., 2000, Brazma et al., 2001) and began work to establish<br />

the ArrayExpress database. As of February 2009 the ArrayExpress Archive holds data from approximately<br />

200,000 microarrays. The ArrayExpress Atlas of Gene Expression allows the users to<br />

query for expression profiles of particular genes, tissues or disease states across multiple experiments.<br />

Our PhD students and postdocs focus mostly on integrative data analysis and on building<br />

models for systems biology (e.g., Rustici et al., 2004, Schlitt & Brazma, 2006).<br />

Alvis Brazma<br />

PhD 1987, Computer<br />

Science, Moscow State<br />

University.<br />

Postdoctoral research in New<br />

Mexico State University, La<br />

Cruses.<br />

Team leader at <strong>EMBL</strong>-EBI<br />

since 2000.<br />

Future projects and goals<br />

A biological system, such as a cell, tissue, organ or organism, can be in many different states, such as developmental stages, disease states, or<br />

physiological states. Different cell types can be considered as different biological states evolving from the progenitor cell state. This poses<br />

many questions; how many different biological<br />

states are there, what are the relationships between<br />

them, which tissue or cell types are more similar to<br />

each other and which are different, how is the biological<br />

state affected by a disease, how much does<br />

gene expression depends on environment, and how<br />

much on genotype? Finding answers to these questions<br />

is one of the most important goals of our<br />

group’s research. Towards this goal we are building<br />

a comprehensive gene expression atlas for human<br />

and model organisms. The Gene Expression Atlas<br />

integrates data from tens of thousands of transcriptomics<br />

assays available in ArrayExpress. We<br />

will also continue large collaborative projects, such<br />

as integration of transcriptomics, proteomics and<br />

human genome variation data to understand the<br />

molecular mechanisms of disease, as well as building<br />

biomedical data analysis infrastructure to help<br />

us in answering these questions.<br />

Visualisation of relationship transcriptomes of ~5,300<br />

human samples categorised in 15 biological classes<br />

using Neighbor Retrieval Visualizer (NeRV; Venna &<br />

Kaski, 2007) developed by our collaborators in<br />

Helsinki University of Technology.<br />

Selected references<br />

Parkinson, H. et al. (2009). ArrayExpress update – from an archive of<br />

functional genomics experiments to the atlas of gene expression.<br />

Nucleic Acids Res., 37, D868-872<br />

Rustici, G. et al. (2007). Global transcriptional responses of fission<br />

and budding yeast to changes in copper and iron levels: a<br />

comparative study. Genome Biol., 8, R73<br />

Schlitt, T. & Brazma, A. (2006). Modelling in molecular biology:<br />

describing transcription regulatory networks at different scales.<br />

Philos. Trans. R. Soc. Lond. B. Biol. Sci., 361, 83-9<br />

Rustici, G. et al. (200). Periodic gene expression program of the<br />

fission yeast cell cycle. Nature Genetics, 36, 809-817<br />

73

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