Evidence map›Paper›PMID 19811632›Full record

ArticleBMC bioinformatics2009

Generation of Gene Ontology benchmark datasets with various types of positive signal.

Petri Törönen, Petri Pehkonen, Liisa Holm

Abstract read
In one paragraph

Article in BMC bioinformatics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Chapter 9: Analyses using disease ontologies.PLoS computational biology · 2012
    Article
  2. Article
  3. An ontology-neutral framework for enrichment analysis.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2010
    Article
  4. Review
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Petri TörönenThe Holm Group, Biocenter II, Institute of Biotechnology, PO Box 56, 00014 University of Helsinki, Finland. petri.toronen@helsinki.fi
Petri Pehkonen
Liisa Holm

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe analysis of over-represented functional classes in a list of genes is one of the most essential bioinformatics research topics. Typical examples of such lists are the differentially expressed genes from transcriptional analysis which need to be linked to functional information represented in the Gene Ontology (GO). Despite the importance of this procedure, there is a little work on consistent evaluation of various GO analysis methods. Especially, there is no literature on creating benchmark datasets for GO analysis tools.

resultsWe propose a methodology for the evaluation of GO analysis tools, which consists of creating gene lists with a selected signal level and a selected number of independent over-represented classes. The methodology starts with a real life GO data matrix, and therefore the generated datasets have similar features to real positive datasets. The user can select the signal level for over-representation, the number of independent positive classes in the dataset, and the size of the final gene list. We present the use of the effective number and various normalizations while embedding the signal to a selected class or classes and the use of binary correlation to ensure that the selected signal classes are independent with each other. The usefulness of generated datasets is demonstrated by comparing different GO class ranking and GO clustering methods.

conclusionThe presented methods aid the development and evaluation of GO analysis methods as they enable thorough testing with different signal types and different signal levels. As an example, our comparisons reveal clear differences between compared GO clustering and GO de-correlation methods. The implementation is coded in Matlab and is freely available at the dedicated website http://ekhidna.biocenter.helsinki.fi/users/petri/public/POSGODA/POSGODA.html.

Indexed as

Databases, GeneticAlgorithmsComputational BiologyInformation Storage and RetrievalUser-Computer Interface

Identifiers

PMID19811632
PMCPMC2762998

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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.