Evidence map›Paper›PMID 22084118›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Construction of regulatory networks using expression time-series data of a genotyped population.

Ka Yee Yeung, Kenneth M Dombek, Kenneth Lo, John E Mittler, Jun Zhu, Eric E Schadt, Roger E Bumgarner, Adrian E Raftery

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.1field-weighted citation impact, top 5% of its field
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

48 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
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  3. Inference of DNA methylation patterns in molluscs.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
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  6. Integration of Multiple Data Sources for Gene Network Inference Using Genetic Perturbation Data.Journal of computational biology : a journal of computational molecular cell biology · 2019
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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

8 authors at 4 institutions in 2 countries.

Ka Yee YeungDepartment of Microbiology, University of Washington, Seattle, WA 98195, USA.
Kenneth M Dombek
Kenneth Lo
John E Mittler
Jun Zhu
Eric E Schadt
Roger E Bumgarner
Adrian E Raftery
University of Washington · USCzech Academy of Sciences, Institute of Microbiology · CZPacific Biosciences (United States) · USSage Bionetworks · US

Funding

Methods and Data CoreR24HD042828 · NICHD · UNIVERSITY OF WASHINGTON · PI MAR, CORINNE M · 2002 to 2016
$9.3M
Statistical Methods for Population ProjectionsR01HD070936 · NICHD · UNIVERSITY OF WASHINGTON · PI RAFTERY, ADRIAN E · 2012 to 2021
$3.3M
Sexually Transmitted Infection Epidemics: Bayesian Prevalence & Size EstimateR01HD054511 · NICHD · UNIVERSITY OF WASHINGTON · PI RAFTERY, ADRIAN E · 2007 to 2016
$3.2M
Prediction and Network Construction Using High-throughput DataR01GM084163 · NIGMS · UNIVERSITY OF WASHINGTON · PI YEUNG-RHEE, KA YEE · 2008 to 2012
$2.6M
NICHD NIH HHS R01 HD054511NICHD NIH HHS R01 HD070936NICHD NIH HHS R01 HD54511NICHD NIH HHS R24 HD042828NIGMS NIH HHS 3R01GM084163-02S2NIGMS NIH HHS 5R01GM084163NIGMS NIH HHS R01 GM084163
6 · The paper itself

Abstract

The inference of regulatory and biochemical networks from large-scale genomics data is a basic problem in molecular biology. The goal is to generate testable hypotheses of gene-to-gene influences and subsequently to design bench experiments to confirm these network predictions. Coexpression of genes in large-scale gene-expression data implies coregulation and potential gene-gene interactions, but provide little information about the direction of influences. Here, we use both time-series data and genetics data to infer directionality of edges in regulatory networks: time-series data contain information about the chronological order of regulatory events and genetics data allow us to map DNA variations to variations at the RNA level. We generate microarray data measuring time-dependent gene-expression levels in 95 genotyped yeast segregants subjected to a drug perturbation. We develop a Bayesian model averaging regression algorithm that incorporates external information from diverse data types to infer regulatory networks from the time-series and genetics data. Our algorithm is capable of generating feedback loops. We show that our inferred network recovers existing and novel regulatory relationships. Following network construction, we generate independent microarray data on selected deletion mutants to prospectively test network predictions. We demonstrate the potential of our network to discover de novo transcription-factor binding sites. Applying our construction method to previously published data demonstrates that our method is competitive with leading network construction algorithms in the literature.

Indexed as

AlgorithmsGenetic VariationModels, BiologicalBayes TheoremBinding SitesGene Expression Regulation, FungalGene Regulatory NetworksLogistic ModelsMetabolic Networks and PathwaysTime FactorsTranscription FactorsYeastsTranscription Factors

Identifiers

PMID22084118
PMCPMC3228453
OpenAlexW2070302210

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.