Evidence map›Paper›PMID 28732468›Full record

ArticleBMC bioinformatics2017

NoGOA: predicting noisy GO annotations using evidences and sparse representation.

Guoxian Yu, Chang Lu, Jun Wang

Abstract read
In one paragraph

Article in BMC bioinformatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

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0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. The Pre-Implantation Embryo Induces Uterine Inflammatory Reaction in Mice.Reproductive sciences (Thousand Oaks, Calif.) · 2021
    Article
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  7. Article
  8. Article
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Guoxian YuCollege of Computer and Information Sciences, Southwest University, Chongqing, China. gxyu@swu.edu.cn.ORCID http://orcid.org/0000-0002-1667-6705
Chang LuCollege of Computer and Information Sciences, Southwest University, Chongqing, China.
Jun WangCollege of Computer and Information Sciences, Southwest University, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGene Ontology (GO) is a community effort to represent functional features of gene products. GO annotations (GOA) provide functional associations between GO terms and gene products. Due to resources limitation, only a small portion of annotations are manually checked by curators, and the others are electronically inferred. Although quality control techniques have been applied to ensure the quality of annotations, the community consistently report that there are still considerable noisy (or incorrect) annotations. Given the wide application of annotations, however, how to identify noisy annotations is an important but yet seldom studied open problem.

resultsWe introduce a novel approach called NoGOA to predict noisy annotations. NoGOA applies sparse representation on the gene-term association matrix to reduce the impact of noisy annotations, and takes advantage of sparse representation coefficients to measure the semantic similarity between genes. Secondly, it preliminarily predicts noisy annotations of a gene based on aggregated votes from semantic neighborhood genes of that gene. Next, NoGOA estimates the ratio of noisy annotations for each evidence code based on direct annotations in GOA files archived on different periods, and then weights entries of the association matrix via estimated ratios and propagates weights to ancestors of direct annotations using GO hierarchy. Finally, it integrates evidence-weighted association matrix and aggregated votes to predict noisy annotations. Experiments on archived GOA files of six model species (H. sapiens, A. thaliana, S. cerevisiae, G. gallus, B. Taurus and M. musculus) demonstrate that NoGOA achieves significantly better results than other related methods and removing noisy annotations improves the performance of gene function prediction.

conclusionsThe comparative study justifies the effectiveness of integrating evidence codes with sparse representation for predicting noisy GO annotations. Codes and datasets are available at http://mlda.swu.edu.cn/codes.php?name=NoGOA .

Indexed as

Gene OntologyAnimalsArabidopsisCattleChickensComputational BiologyHumansMiceMolecular Sequence AnnotationSaccharomyces cerevisiaeEvidence codesGene ontologyGO annotationsSparse representation

Identifiers

PMID28732468
PMCPMC5521088

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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.