Scinovex
article Open AccessTop 1% cited

PredictSNP: Robust and Accurate Consensus Classifier for Prediction of Disease-Related Mutations

PLoS Computational Biology · 2014 · Vol. 10(1) · pp. e1003440–e1003440
Jaroslav BendlJan ŠtouračOndrej SalandaAntonín PavelkaEric D. WiebenJaroslav ZendulkaJan BrezovskýJiřı́ Damborský

Abstract

Single nucleotide variants represent a prevalent form of genetic variation. Mutations in the coding regions are frequently associated with the development of various genetic diseases. Computational tools for the prediction of the effects of mutations on protein function are very important for analysis of single nucleotide variants and their prioritization for experimental characterization. Many computational tools are already widely employed for this purpose. Unfortunately, their comparison and further improvement is hindered by large overlaps between the training datasets and benchmark datasets, which lead to biased and overly optimistic reported performances. In this study, we have constructed three independent datasets by removing all duplicities, inconsistencies and mutations previously used in the training of evaluated tools. The benchmark dataset containing over 43,000 mutations was employed for the unbiased evaluation of eight established prediction tools: MAPP, nsSNPAnalyzer, PANTHER, PhD-SNP, PolyPhen-1, PolyPhen-2, SIFT and SNAP. The six best performing tools were combined into a consensus classifier PredictSNP, resulting into significantly improved prediction performance, and at the same time returned results for all mutations, confirming that consensus prediction represents an accurate and robust alternative to the predictions delivered by individual tools. A user-friendly web interface enables easy access to all eight prediction tools, the consensus classifier PredictSNP and annotations from the Protein Mutant Database and the UniProt database. The web server and the datasets are freely available to the academic community at http://loschmidt.chemi.muni.cz/predictsnp.

Genomics and Rare DiseasesGenomics and Phylogenetic StudiesMachine Learning in BioinformaticsComputer scienceClassifier (UML)Machine learningArtificial intelligenceData mining

MeSH terms

AlgorithmsComputer SimulationHumansMutationPhylogenySoftwareGenetic VariationGenome, HumanComputational BiologyInternetPolymorphism, Single NucleotideGenetic Diseases, InbornDatabases, Protein

Funding

  • European Regional Development Fund
Citations
864
FWCI
31.27
field-weighted impact
References
69
Percentile
100%
vs. same field & year
Citations per year
Cited by
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants
The American Journal of Human Genetics · 2016 · 2,867 citations
References
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.