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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 />
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