Evidence map›Paper›PMID 28301504›Full record

ArticlePloS one2017

Identification of marginal causal relationships in gene networks from observational and interventional expression data.

Gilles Monneret, Florence Jaffrézic, Andrea Rau, Tatiana Zerjal, Grégory Nuel

Abstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Gilles MonneretUMR GABI, AgroParisTech, INRA, Université Paris-Saclay, 78350 Jouy-en-Josas, France.
Florence JaffrézicUMR GABI, AgroParisTech, INRA, Université Paris-Saclay, 78350 Jouy-en-Josas, France.
Andrea RauUMR GABI, AgroParisTech, INRA, Université Paris-Saclay, 78350 Jouy-en-Josas, France.
Tatiana ZerjalUMR GABI, AgroParisTech, INRA, Université Paris-Saclay, 78350 Jouy-en-Josas, France.
Grégory NuelLPMA, UMR CNRS 7599, UPMC, Sorbonne Universités, 4 place Jussieu, 75005 Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Causal network inference is an important methodological challenge in biology as well as other areas of application. Although several causal network inference methods have been proposed in recent years, they are typically applicable for only a small number of genes, due to the large number of parameters to be estimated and the limited number of biological replicates available. In this work, we consider the specific case of transcriptomic studies made up of both observational and interventional data in which a single gene of biological interest is knocked out. We focus on a marginal causal estimation approach, based on the framework of Gaussian directed acyclic graphs, to infer causal relationships between the knocked-out gene and a large set of other genes. In a simulation study, we found that our proposed method accurately differentiates between downstream causal relationships and those that are upstream or simply associative. It also enables an estimation of the total causal effects between the gene of interest and the remaining genes. Our method performed very similarly to a classical differential analysis for experiments with a relatively large number of biological replicates, but has the advantage of providing a formal causal interpretation. Our proposed marginal causal approach is computationally efficient and may be applied to several thousands of genes simultaneously. In addition, it may help highlight subsets of genes of interest for a more thorough subsequent causal network inference. The method is implemented in an R package called MarginalCausality (available on GitHub).

Indexed as

Gene ExpressionGene Regulatory NetworksGene Knockout TechniquesModels, TheoreticalReproducibility of Results

Identifiers

PMID28301504
PMCPMC5354375

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.