Evidence map›Paper›PMID 26394325›Full record

ArticlePloS one2015

Time Delayed Causal Gene Regulatory Network Inference with Hidden Common Causes.

Leung-Yau Lo, Man-Leung Wong, Kin-Hong Lee, Kwong-Sak Leung

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Leung-Yau LoDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
Man-Leung WongDepartment of Computing and Decision Sciences, Lingnan University, Tuen Mun, Hong Kong.
Kin-Hong LeeDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
Kwong-Sak LeungDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong, Hong Kong.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inferring the gene regulatory network (GRN) is crucial to understanding the working of the cell. Many computational methods attempt to infer the GRN from time series expression data, instead of through expensive and time-consuming experiments. However, existing methods make the convenient but unrealistic assumption of causal sufficiency, i.e. all the relevant factors in the causal network have been observed and there are no unobserved common cause. In principle, in the real world, it is impossible to be certain that all relevant factors or common causes have been observed, because some factors may not have been conceived of, and therefore are impossible to measure. In view of this, we have developed a novel algorithm named HCC-CLINDE to infer an GRN from time series data allowing the presence of hidden common cause(s). We assume there is a sparse causal graph (possibly with cycles) of interest, where the variables are continuous and each causal link has a delay (possibly more than one time step). A small but unknown number of variables are not observed. Each unobserved variable has only observed variables as children and parents, with at least two children, and the children are not linked to each other. Since it is difficult to obtain very long time series, our algorithm is also capable of utilizing multiple short time series, which is more realistic. To our knowledge, our algorithm is far less restrictive than previous works. We have performed extensive experiments using synthetic data on GRNs of size up to 100, with up to 10 hidden nodes. The results show that our algorithm can adequately recover the true causal GRN and is robust to slight deviation from Gaussian distribution in the error terms. We have also demonstrated the potential of our algorithm on small YEASTRACT subnetworks using limited real data.

Indexed as

AlgorithmsGene Regulatory NetworksModels, GeneticComputational BiologyDatabases, GeneticGene Expression ProfilingGene Expression RegulationKineticsReproducibility of ResultsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTime FactorsSaccharomyces cerevisiae Proteins

Identifiers

PMID26394325
PMCPMC4578777

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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.