ArticleBMC bioinformatics2017
NoGOA: predicting noisy GO annotations using evidences and sparse representation.
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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8 citing papers in PubMed.
- HEC-ASD: a hybrid ensemble-based classification model for predicting autism spectrum disorder disease genes.BMC bioinformatics · 2022Article
- Propagation, detection and correction of errors using the sequence database network.Briefings in bioinformatics · 2022Review
- Computational Methods for Prediction of Human Protein-Phenotype Associations: A Review.Phenomics (Cham, Switzerland) · 2021Review
- Ensemble of Multiple Classifiers for Multilabel Classification of Plant Protein Subcellular Localization.Life (Basel, Switzerland) · 2021Article
- The Pre-Implantation Embryo Induces Uterine Inflammatory Reaction in Mice.Reproductive sciences (Thousand Oaks, Calif.) · 2021Article
- A Literature Review of Gene Function Prediction by Modeling Gene Ontology.Frontiers in genetics · 2020Review
- Expression Profile Analysis of Differentially Expressed Circular RNAs in Steroid-Induced Osteonecrosis of the Femoral Head.Disease markers · 2019Article
- Monitoring changes in the Gene Ontology and their impact on genomic data analysis.GigaScience · 2018Article
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3 authors.
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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 .
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