Evidence map›Paper›PMID 24931990›Full record

ArticleBioinformatics (Oxford, England)2014

Gene network inference by probabilistic scoring of relationships from a factorized model of interactions.

Marinka Zitnik, Blaž Zupan

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 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

2 authors.

Marinka ZitnikFaculty of Computer and Information Science, University of Ljubljana, SI-1000 Ljubljana, Slovenia and Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Blaž ZupanFaculty of Computer and Information Science, University of Ljubljana, SI-1000 Ljubljana, Slovenia and Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USAFaculty of Computer and Information Science, University of Ljubljana, SI-1000 Ljubljana, Slovenia and Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

Funding

PROJECT III - Computational Analysis of Phenotypes andP01HD039691 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI SUCGANG, RICHARD · 2001 to 2016
$14.4M
NICHD NIH HHS P01 HD039691NICHD NIH HHS P01-HD39691
6 · The paper itself

Abstract

motivationEpistasis analysis is an essential tool of classical genetics for inferring the order of function of genes in a common pathway. Typically, it considers single and double mutant phenotypes and for a pair of genes observes whether a change in the first gene masks the effects of the mutation in the second gene. Despite the recent emergence of biotechnology techniques that can provide gene interaction data on a large, possibly genomic scale, few methods are available for quantitative epistasis analysis and epistasis-based network reconstruction.

resultsWe here propose a conceptually new probabilistic approach to gene network inference from quantitative interaction data. The approach is founded on epistasis analysis. Its features are joint treatment of the mutant phenotype data with a factorized model and probabilistic scoring of pairwise gene relationships that are inferred from the latent gene representation. The resulting gene network is assembled from scored pairwise relationships. In an experimental study, we show that the proposed approach can accurately reconstruct several known pathways and that it surpasses the accuracy of current approaches. AVAILABILITY AND IMPLEMENTATION: Source code is available at http://github.com/biolab/red.

Indexed as

Epistasis, GeneticGene Regulatory NetworksModels, StatisticalAlgorithmsEndoplasmic Reticulum-Associated DegradationGlycosylationMutationPhenotypePhosphatidylserinesPhosphatidylserines

Identifiers

PMID24931990
PMCPMC4229904

What OpenQuestion holds

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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.