Evidence map›Paper›PMID 24742092›Full record

ArticleBMC systems biology2014

Fast Bayesian inference for gene regulatory networks using ScanBMA.

William Chad Young, Adrian E Raftery, Ka Yee Yeung

Abstract read
In one paragraph

Article in BMC systems biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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

40 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Effect of model space priors on statistical inference with model uncertainty.The New England Journal of Statistics in Data Science · 2023
    Article
  5. Review
  6. Article
  7. Article
  8. Comparing methods for statistical inference with model uncertainty.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Article
  10. Article
  11. Probabilistic Graphical Models Applied to Biological Networks.Advances in experimental medicine and biology · 2021
    Article
  12. Article
  13. Article
  14. 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
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

William Chad Young
Adrian E Raftery
Ka Yee YeungDepartment of Microbiology, University of Washington, Box 357735, 98195-7735, Seattle WA, USA. kayee@uw.edu.

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 HD054511NICHD NIH HHS R01 HD070936NICHD NIH HHS R24 HD042828NIGMS NIH HHS 3R01GM084163-05S1NIGMS NIH HHS 5R01GM084163NIGMS NIH HHS R01 GM084163
6 · The paper itself

Abstract

backgroundGenome-wide time-series data provide a rich set of information for discovering gene regulatory relationships. As genome-wide data for mammalian systems are being generated, it is critical to develop network inference methods that can handle tens of thousands of genes efficiently, provide a systematic framework for the integration of multiple data sources, and yield robust, accurate and compact gene-to-gene relationships.

resultsWe developed and applied ScanBMA, a Bayesian inference method that incorporates external information to improve the accuracy of the inferred network. In particular, we developed a new strategy to efficiently search the model space, applied data transformations to reduce the effect of spurious relationships, and adopted the g-prior to guide the search for candidate regulators. Our method is highly computationally efficient, thus addressing the scalability issue with network inference. The method is implemented as the ScanBMA function in the networkBMA Bioconductor software package.

conclusionsWe compared ScanBMA to other popular methods using time series yeast data as well as time-series simulated data from the DREAM competition. We found that ScanBMA produced more compact networks with a greater proportion of true positives than the competing methods. Specifically, ScanBMA generally produced more favorable areas under the Receiver-Operating Characteristic and Precision-Recall curves than other regression-based methods and mutual-information based methods. In addition, ScanBMA is competitive with other network inference methods in terms of running time.

Indexed as

Gene Regulatory NetworksAlgorithmsBayes TheoremGenomicsSaccharomyces cerevisiae

Identifiers

PMID24742092
PMCPMC4006459

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.