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.

Highlights

  • The single nucleotide variants (SNVs) are the most frequent type of genetic variation in humans, responsible for almost 90% of known sequence differences [1,2]

  • The benchmark dataset used for the evaluation of the selected prediction tools and training of consensus classifier PredictSNP was compiled from five different sources

  • The subset of Protein Mutant Database (PMD) testing dataset containing only the mutations associated with sequences from the UniProt database, called PMD-UNIPROT, was prepared to enable the evaluation by CONDEL during the comparison of PredictSNP classifier to other consensus classifiers

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Summary

Introduction

The single nucleotide variants (SNVs) are the most frequent type of genetic variation in humans, responsible for almost 90% of known sequence differences [1,2]. The benchmark dataset used for the evaluation of the selected prediction tools and training of consensus classifier PredictSNP was compiled from five different sources. As a complement to the independent PredictSNP benchmark dataset, another dataset containing only mutations present in the training sets of evaluated tools (nsSNPAnalyzer, PhD-SNP, PolyPhen-2 and SNAP) was compiled.

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