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A generalized framework for controlling FDR in gene regulatory network inference
Stockholm Univ, Sweden.
Linköpings universitet, Institutionen för fysik, kemi och biologi, Bioinformatik. Linköpings universitet, Tekniska fakulteten.
Natl Cheng Kung Univ, Taiwan.
Stockholm Univ, Sweden.
2019 (engelsk)Inngår i: Bioinformatics, ISSN 1367-4803, E-ISSN 1367-4811, Vol. 35, nr 6, s. 1026-1032Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Motivation Inference of gene regulatory networks (GRNs) from perturbation data can give detailed mechanistic insights of a biological system. Many inference methods exist, but the resulting GRN is generally sensitive to the choice of method-specific parameters. Even though the inferred GRN is optimal given the parameters, many links may be wrong or missing if the data is not informative. To make GRN inference reliable, a method is needed to estimate the support of each predicted link as the method parameters are varied. Results To achieve this we have developed a method called nested bootstrapping, which applies a bootstrapping protocol to GRN inference, and by repeated bootstrap runs assesses the stability of the estimated support values. To translate bootstrap support values to false discovery rates we run the same pipeline with shuffled data as input. This provides a general method to control the false discovery rate of GRN inference that can be applied to any setting of inference parameters, noise level, or data properties. We evaluated nested bootstrapping on a simulated dataset spanning a range of such properties, using the LASSO, Least Squares, RNI, GENIE3 and CLR inference methods. An improved inference accuracy was observed in almost all situations. Nested bootstrapping was incorporated into the GeneSPIDER package, which was also used for generating the simulated networks and data, as well as running and analyzing the inferences. Availability and implementation https://bitbucket.org/sonnhammergrni/genespider/src/NB/%2B Methods/NestBoot.m

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OXFORD UNIV PRESS , 2019. Vol. 35, nr 6, s. 1026-1032
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Identifikatorer
URN: urn:nbn:se:liu:diva-156395DOI: 10.1093/bioinformatics/bty764ISI: 000462709200016PubMedID: 30169550OAI: oai:DiVA.org:liu-156395DiVA, id: diva2:1305716
Merknad

Funding Agencies|National Cheng Kung University; Ministry of Science and Technology in Taiwan [105-2218-E-006-016-MY2]

Tilgjengelig fra: 2019-04-18 Laget: 2019-04-18 Sist oppdatert: 2019-04-18

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