Difference between revisions of "Research"
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==Collaborators== | ==Collaborators== | ||
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*Edward Marcotte, University of Texas at Austin, USA | *Edward Marcotte, University of Texas at Austin, USA | ||
*Andrew Fraser, University of Toronto, Canada | *Andrew Fraser, University of Toronto, Canada | ||
− | Ben Lehner, Systems Biology Unit, EMBL-CRG, Spain | + | *Ben Lehner, Systems Biology Unit, EMBL-CRG, Spain |
− | Sue Rhee, Carnegie Institution of Science, USA | + | *Sue Rhee, Carnegie Institution of Science, USA |
− | Pamela Ronald, University of California at Davis, USA | + | *Pamela Ronald, University of California at Davis, USA |
− | Matthew Hurles, Sanger Institute, UK | + | *Matthew Hurles, Sanger Institute, UK |
− | Philip Benfey, Duke University, USA | + | *Philip Benfey, Duke University, USA |
− | Sangsun Yoon, Yonsei Medical School, Korea | + | *Sangsun Yoon, Yonsei Medical School, Korea |
− | Dongryul Lee, Cha Medical School, Korea | + | *Dongryul Lee, Cha Medical School, Korea |
− | Yongsun Bahn, Yonsei University, Korea | + | *Yongsun Bahn, Yonsei University, Korea |
− | Sangjun Ha, Yonsei University, Korea | + | *Sangjun Ha, Yonsei University, Korea |
==Functional Networks== | ==Functional Networks== |
Revision as of 16:09, 9 April 2011
Research Summary
The ultimate goal of biological research is to manipulate traits that are important for medicine, agriculture, and bio-industry. This challenging task first requires good understanding of association between genotype and phenotype. Because of high complexity of genotype as well as phenotype, complexity of the genotype-phenotype association could be even untouchable by combinatorial explosion of the number of possible associations. Therefore, modern genetics needs to be more systematic and predictive. Recently we proposed network-guided approach for genetics of complex traits. First, we construct probabilistic functional gene networks for cells or organisms by benchmarking and integrating heterogeneous multi-omics data that are in general publicly available. Then, using guilt-by-association, and other algorithms of network propagation of known biological information, we predict gene functions, phenotypic effect of loss-of-function, and epistatic interaction. The information can contribute to reconstruction of map between genotype and phenotype. The network-guided genetics method has been effectively applied for various organisms; from simple microbe yeast, to multicellular animal C. elegans, to the reference plant Arabidopsis, to the reference crop rice, and to the human.
Collaborators
- Edward Marcotte, University of Texas at Austin, USA
- Andrew Fraser, University of Toronto, Canada
- Ben Lehner, Systems Biology Unit, EMBL-CRG, Spain
- Sue Rhee, Carnegie Institution of Science, USA
- Pamela Ronald, University of California at Davis, USA
- Matthew Hurles, Sanger Institute, UK
- Philip Benfey, Duke University, USA
- Sangsun Yoon, Yonsei Medical School, Korea
- Dongryul Lee, Cha Medical School, Korea
- Yongsun Bahn, Yonsei University, Korea
- Sangjun Ha, Yonsei University, Korea