Evidence map›Paper›PMID 29020744›Full record

ArticleGigaScience2017

fastBMA: scalable network inference and transitive reduction.

Ling-Hong Hung, Kaiyuan Shi, Migao Wu, William Chad Young, Adrian E Raftery, Ka Yee Yeung

Abstract read
In one paragraph

Article in GigaScience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. 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
  4. Review
  5. Article
  6. Article
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

6 authors.

Ling-Hong HungInstitute of Technology, University of Washington, Tacoma Campus, Box 358426, 1900 Commerce Street, Tacoma, WA 98402-3100, U.S.A.
Kaiyuan ShiInstitute of Technology, University of Washington, Tacoma Campus, Box 358426, 1900 Commerce Street, Tacoma, WA 98402-3100, U.S.A.
Migao WuInstitute of Technology, University of Washington, Tacoma Campus, Box 358426, 1900 Commerce Street, Tacoma, WA 98402-3100, U.S.A.
William Chad YoungDepartment of Statistics, University of Washington, Box 354322, Seattle, WA 98195-4322, U.S.A.
Adrian E RafteryDepartment of Statistics, University of Washington, Box 354322, Seattle, WA 98195-4322, U.S.A.
Ka Yee YeungInstitute of Technology, University of Washington, Tacoma Campus, Box 358426, 1900 Commerce Street, Tacoma, WA 98402-3100, U.S.A.

Funding

Data Coordination and Integration Center for LINCS-BD2KU54HL127624 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MA'AYAN, AVI, SCHURER, STEPHAN C · 2014 to 2019
$23.5M
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
NHLBI NIH HHS U54 HL127624NICHD NIH HHS R01 HD054511NICHD NIH HHS R01 HD070936
6 · The paper itself

Abstract

Inferring genetic networks from genome-wide expression data is extremely demanding computationally. We have developed fastBMA, a distributed, parallel, and scalable implementation of Bayesian model averaging (BMA) for this purpose. fastBMA also includes a computationally efficient module for eliminating redundant indirect edges in the network by mapping the transitive reduction to an easily solved shortest-path problem. We evaluated the performance of fastBMA on synthetic data and experimental genome-wide time series yeast and human datasets. When using a single CPU core, fastBMA is up to 100 times faster than the next fastest method, LASSO, with increased accuracy. It is a memory-efficient, parallel, and distributed application that scales to human genome-wide expression data. A 10 000-gene regulation network can be obtained in a matter of hours using a 32-core cloud cluster (2 nodes of 16 cores). fastBMA is a significant improvement over its predecessor ScanBMA. It is more accurate and orders of magnitude faster than other fast network inference methods such as the 1 based on LASSO. The improved scalability allows it to calculate networks from genome scale data in a reasonable time frame. The transitive reduction method can improve accuracy in denser networks. fastBMA is available as code (M.I.T. license) from GitHub (https://github.com/lhhunghimself/fastBMA), as part of the updated networkBMA Bioconductor package (https://www.bioconductor.org/packages/release/bioc/html/networkBMA.html) and as ready-to-deploy Docker images (https://hub.docker.com/r/biodepot/fastbma/).

Indexed as

AlgorithmsGene Regulatory NetworksGenome, FungalGenome, HumanBayes TheoremGene ExpressionHumansModels, StatisticalSaccharomyces cerevisiaeBayesian modelsBloom filterCholesky decompositionDijkstra's algorithmdistributed computingDocker containergene regulationnetwork inferenceoptimized software findingstime series

Identifiers

PMID29020744
PMCPMC5632288

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.