Evidence map›Paper›PMID 20529941›Full record

ArticleBioinformatics (Oxford, England)2010

Assessing the functional coherence of gene sets with metrics based on the Gene Ontology graph.

Adam J Richards, Brian Muller, Matthew Shotwell, L Ashley Cowart, Bäerbel Rohrer, Xinghua Lu

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Functional coherence metrics in protein families.Journal of biomedical semantics · 2016
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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

6 authors.

Adam J RichardsDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, USA.
Brian Muller
Matthew Shotwell
L Ashley Cowart
Bäerbel Rohrer
Xinghua Lu

Funding

Training of Toolmakers for Bio-Medical Informatics (TTB*T15LM007438 · NLM · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI LU, XINGHUA · 2002 to 2008
$1.6M
ROD NEURODEGENERATIVE AND PROTECTIVE GENESR01EY013520 · NEI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ROHRER, BAERBEL · 2001 to 2005
$1.6M
Statistical methods for integromics discoveriesR01LM010144 · NLM · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LU, XINGHUA · 2009 to 2013
$1.6M
Automatic Literature-based Protein AnnotationR01LM009153 · NLM · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LU, XINGHUA · 2007 to 2009
$1.0M
NCRR NIH HHS 2P20RR107677NEI NIH HHS R01 EY013520NEI NIH HHS R01EY13520NLM NIH HHS 5R01LM010144NLM NIH HHS R01 LM009153NLM NIH HHS R01LM009153NLM NIH HHS R01 LM010144NLM NIH HHS T15 LM007438NLM NIH HHS T15LM07438
6 · The paper itself

Abstract

motivationThe results of initial analyses for many high-throughput technologies commonly take the form of gene or protein sets, and one of the ensuing tasks is to evaluate the functional coherence of these sets. The study of gene set function most commonly makes use of controlled vocabulary in the form of ontology annotations. For a given gene set, the statistical significance of observing these annotations or 'enrichment' may be tested using a number of methods. Instead of testing for significance of individual terms, this study is concerned with the task of assessing the global functional coherence of gene sets, for which novel metrics and statistical methods have been devised.

resultsThe metrics of this study are based on the topological properties of graphs comprised of genes and their Gene Ontology annotations. A novel aspect of these methods is that both the enrichment of annotations and the relationships among annotations are considered when determining the significance of functional coherence. We applied our methods to perform analyses on an existing database and on microarray experimental results. Here, we demonstrated that our approach is highly discriminative in terms of differentiating coherent gene sets from random ones and that it provides biologically sensible evaluations in microarray analysis. We further used examples to show the utility of graph visualization as a tool for studying the functional coherence of gene sets. AVAILABILITY: The implementation is provided as a freely accessible web application at: http://projects.dbbe.musc.edu/gosteiner. Additionally, the source code written in the Python programming language, is available under the General Public License of the Free Software Foundation. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

GenesAnimalsComputational BiologyDatabases, GeneticGene Expression ProfilingHumansSoftware

Identifiers

PMID20529941
PMCPMC2881388

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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.