Maximal extraction of biological information from genetic interaction data.

Extraction of all the biological information inherent in large-scale genetic interaction datasets remains a significant challenge for systems biology. The core problem is essentially that of classification of the relationships among phenotypes of mutant strains into biologically informative "ru...

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Main Authors: Gregory W Carter, David J Galas, Timothy Galitski
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-04-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC2659753?pdf=render
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spelling doaj-457d426057ce46849b9ab615ebbe70642020-11-25T01:44:39ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582009-04-0154e100034710.1371/journal.pcbi.1000347Maximal extraction of biological information from genetic interaction data.Gregory W CarterDavid J GalasTimothy GalitskiExtraction of all the biological information inherent in large-scale genetic interaction datasets remains a significant challenge for systems biology. The core problem is essentially that of classification of the relationships among phenotypes of mutant strains into biologically informative "rules" of gene interaction. Geneticists have determined such classifications based on insights from biological examples, but it is not clear that there is a systematic, unsupervised way to extract this information. In this paper we describe such a method that depends on maximizing a previously described context-dependent information measure to obtain maximally informative biological networks. We have successfully validated this method on two examples from yeast by demonstrating that more biological information is obtained when analysis is guided by this information measure. The context-dependent information measure is a function only of phenotype data and a set of interaction rules, involving no prior biological knowledge. Analysis of the resulting networks reveals that the most biologically informative networks are those with the greatest context-dependent information scores. We propose that these high-complexity networks reveal genetic architecture at a modular level, in contrast to classical genetic interaction rules that order genes in pathways. We suggest that our analysis represents a powerful, data-driven, and general approach to genetic interaction analysis, with particular potential in the study of mammalian systems in which interactions are complex and gene annotation data are sparse.http://europepmc.org/articles/PMC2659753?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Gregory W Carter
David J Galas
Timothy Galitski
spellingShingle Gregory W Carter
David J Galas
Timothy Galitski
Maximal extraction of biological information from genetic interaction data.
PLoS Computational Biology
author_facet Gregory W Carter
David J Galas
Timothy Galitski
author_sort Gregory W Carter
title Maximal extraction of biological information from genetic interaction data.
title_short Maximal extraction of biological information from genetic interaction data.
title_full Maximal extraction of biological information from genetic interaction data.
title_fullStr Maximal extraction of biological information from genetic interaction data.
title_full_unstemmed Maximal extraction of biological information from genetic interaction data.
title_sort maximal extraction of biological information from genetic interaction data.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2009-04-01
description Extraction of all the biological information inherent in large-scale genetic interaction datasets remains a significant challenge for systems biology. The core problem is essentially that of classification of the relationships among phenotypes of mutant strains into biologically informative "rules" of gene interaction. Geneticists have determined such classifications based on insights from biological examples, but it is not clear that there is a systematic, unsupervised way to extract this information. In this paper we describe such a method that depends on maximizing a previously described context-dependent information measure to obtain maximally informative biological networks. We have successfully validated this method on two examples from yeast by demonstrating that more biological information is obtained when analysis is guided by this information measure. The context-dependent information measure is a function only of phenotype data and a set of interaction rules, involving no prior biological knowledge. Analysis of the resulting networks reveals that the most biologically informative networks are those with the greatest context-dependent information scores. We propose that these high-complexity networks reveal genetic architecture at a modular level, in contrast to classical genetic interaction rules that order genes in pathways. We suggest that our analysis represents a powerful, data-driven, and general approach to genetic interaction analysis, with particular potential in the study of mammalian systems in which interactions are complex and gene annotation data are sparse.
url http://europepmc.org/articles/PMC2659753?pdf=render
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