Literature DB >> 19178140

Reverse engineering molecular regulatory networks from microarray data with qp-graphs.

Robert Castelo1, Alberto Roverato.   

Abstract

Reverse engineering bioinformatic procedures applied to high-throughput experimental data have become instrumental in generating new hypotheses about molecular regulatory mechanisms. This has been particularly the case for gene expression microarray data, where a large number of statistical and computational methodologies have been developed in order to assist in building network models of transcriptional regulation. A major challenge faced by every different procedure is that the number of available samples n for estimating the network model is much smaller than the number of genes p forming the system under study. This compromises many of the assumptions on which the statistics of the methods rely, often leading to unstable performance figures. In this work, we apply a recently developed novel methodology based in the so-called q-order limited partial correlation graphs, qp-graphs, which is specifically tailored towards molecular network discovery from microarray expression data with p >> n. Using experimental and functional annotation data from Escherichia coli, here we show how qp-graphs yield more stable performance figures than other state-of-the-art methods when the ratio of genes to experiments exceeds one order of magnitude. More importantly, we also show that the better performance of the qp-graph method on such a gene-to-sample ratio has a decisive impact on the functional coherence of the reverse-engineered transcriptional regulatory modules and becomes crucial in such a challenging situation in order to enable the discovery of a network of reasonable confidence that includes a substantial number of genes relevant to the essayed conditions. An R package, called qpgraph implementing this method is part of the Bioconductor project and can be downloaded from (www.bioconductor.org). A parallel standalone version for the most computationally expensive calculations is available from (http://functionalgenomics.upf.xsedu/qpgraph).

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Year:  2009        PMID: 19178140     DOI: 10.1089/cmb.2008.08TT

Source DB:  PubMed          Journal:  J Comput Biol        ISSN: 1066-5277            Impact factor:   1.479


  27 in total

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3.  Mapping eQTL networks with mixed graphical Markov models.

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Journal:  Genetics       Date:  2014-09-29       Impact factor: 4.562

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5.  Systemic alterations in the metabolome of diabetic NOD mice delineate increased oxidative stress accompanied by reduced inflammation and hypertriglyceremia.

Authors:  Johannes Fahrmann; Dmitry Grapov; Jun Yang; Bruce Hammock; Oliver Fiehn; Graeme I Bell; Manami Hara
Journal:  Am J Physiol Endocrinol Metab       Date:  2015-04-07       Impact factor: 4.310

6.  A comprehensive assessment of methods for de-novo reverse-engineering of genome-scale regulatory networks.

Authors:  Varun Narendra; Nikita I Lytkin; Constantin F Aliferis; Alexander Statnikov
Journal:  Genomics       Date:  2010-10-14       Impact factor: 5.736

7.  Inferring regulatory networks from expression data using tree-based methods.

Authors:  Vân Anh Huynh-Thu; Alexandre Irrthum; Louis Wehenkel; Pierre Geurts
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8.  Selecting high-dimensional mixed graphical models using minimal AIC or BIC forests.

Authors:  David Edwards; Gabriel C G de Abreu; Rodrigo Labouriau
Journal:  BMC Bioinformatics       Date:  2010-01-11       Impact factor: 3.169

9.  Identification of self-regulatory network motifs in reverse engineering gene regulatory networks using microarray gene expression data.

Authors:  Mehrosh Khalid; Sharifullah Khan; Jamil Ahmad; Muhammad Shaheryar
Journal:  IET Syst Biol       Date:  2019-04       Impact factor: 1.615

10.  Exploratory and inferential analysis of gene cluster neighborhood graphs.

Authors:  Theresa Scharl; Ingo Voglhuber; Friedrich Leisch
Journal:  BMC Bioinformatics       Date:  2009-09-14       Impact factor: 3.169

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