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pubmed-article:18718939pubmed:issue21lld:pubmed
pubmed-article:18718939pubmed:dateCreated2008-10-21lld:pubmed
pubmed-article:18718939pubmed:abstractTextNested effects models (NEMs) are a class of probabilistic models introduced to analyze the effects of gene perturbation screens visible in high-dimensional phenotypes like microarrays or cell morphology. NEMs reverse engineer upstream/downstream relations of cellular signaling cascades. NEMs take as input a set of candidate pathway genes and phenotypic profiles of perturbing these genes. NEMs return a pathway structure explaining the observed perturbation effects. Here, we describe the package nem, an open-source software to efficiently infer NEMs from data. Our software implements several search algorithms for model fitting and is applicable to a wide range of different data types and representations. The methods we present summarize the current state-of-the-art in NEMs. AVAILABILITY: Our software is written in the R language and freely avail-able via the Bioconductor project at http://www.bioconductor.org.lld:pubmed
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pubmed-article:18718939pubmed:pagination2549-50lld:pubmed
pubmed-article:18718939pubmed:dateRevised2010-9-21lld:pubmed
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pubmed-article:18718939pubmed:year2008lld:pubmed
pubmed-article:18718939pubmed:articleTitleAnalyzing gene perturbation screens with nested effects models in R and bioconductor.lld:pubmed
pubmed-article:18718939pubmed:affiliationGerman Cancer Research Center, INF 580, 69120 Heidelberg, Germany.lld:pubmed
pubmed-article:18718939pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:18718939pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
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pubmed-article:18718939pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed
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