Evidence map›Paper›PMID 27555837›Full record

ArticleFrontiers in microbiology2016

A Bayesian Framework for the Classification of Microbial Gene Activity States.

Craig Disselkoen, Brian Greco, Kaitlyn Cook, Kristin Koch, Reginald Lerebours, Chase Viss, Joshua Cape, Elizabeth Held, Yonatan Ashenafi, Karen Fischer and 5 more

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

15 authors.

Craig DisselkoenDepartment of Mathematics, Statistics and Computer Science, Dordt College Sioux Center, IA, USA.
Brian GrecoDepartment of Biostatistics, School of Public Health, University of MichiganAnn Arbor, MI, USA; Department of Statistics, University of TexasAustin, TX, USA.
Kaitlyn CookDepartment of Biostatistics, Harvard University Boston, MA, USA.
Kristin KochDepartment of Statistics, Baylor University Waco, TX, USA.
Reginald LereboursDepartment of Biostatistics, Harvard University Boston, MA, USA.
Chase VissDepartment of Mathematics, University of Denver Denver, CO, USA.
Joshua CapeDepartment of Applied Mathematics and Statistics, Johns Hopkins University Baltimore, MD, USA.
Elizabeth HeldDepartment of Biostatistics, University of Iowa Iowa City, IA, USA.
Yonatan AshenafiDepartment of Mathematics, Statistics and Computer Science, Dordt College Sioux Center, IA, USA.
Karen FischerDepartment of Statistics, Texas A&M University College Station, TX, USA.
Allyson AcostaDepartment of Computer Science, Hope College Holland, MI, USA.
Mark CunninghamDepartment of Biology, Hope College Holland, MI, USA.
Aaron A BestDepartment of Biology, Hope College Holland, MI, USA.
Matthew DeJonghDepartment of Computer Science, Hope College Holland, MI, USA.
Nathan TintleDepartment of Mathematics, Statistics and Computer Science, Dordt College Sioux Center, IA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Numerous methods for classifying gene activity states based on gene expression data have been proposed for use in downstream applications, such as incorporating transcriptomics data into metabolic models in order to improve resulting flux predictions. These methods often attempt to classify gene activity for each gene in each experimental condition as belonging to one of two states: active (the gene product is part of an active cellular mechanism) or inactive (the cellular mechanism is not active). These existing methods of classifying gene activity states suffer from multiple limitations, including enforcing unrealistic constraints on the overall proportions of active and inactive genes, failing to leverage a priori knowledge of gene co-regulation, failing to account for differences between genes, and failing to provide statistically meaningful confidence estimates. We propose a flexible Bayesian approach to classifying gene activity states based on a Gaussian mixture model. The model integrates genome-wide transcriptomics data from multiple conditions and information about gene co-regulation to provide activity state confidence estimates for each gene in each condition. We compare the performance of our novel method to existing methods on both simulated data and real data from 907 E. coli gene expression arrays, as well as a comparison with experimentally measured flux values in 29 conditions, demonstrating that our method provides more consistent and accurate results than existing methods across a variety of metrics.

Indexed as

bacteriaBayesian modelgene activitygene expressionmetabolic modeling

Identifiers

PMID27555837
PMCPMC4977825

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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.