Ontology highlight
ABSTRACT: Aims
Next-generation sequencing has opened the possibility of large-scale sequence-based disease association studies. A major challenge in interpreting whole-exome data is predicting which of the discovered variants are deleterious or neutral. To address this question in silico, we have developed a score called Combined Annotation scoRing toOL (CAROL), which combines information from 2 bioinformatics tools: PolyPhen-2 and SIFT, in order to improve the prediction of the effect of non-synonymous coding variants.Methods
We used a weighted Z method that combines the probabilistic scores of PolyPhen-2 and SIFT. We defined 2 dataset pairs to train and test CAROL using information from the dbSNP: 'HGMD-PUBLIC' and 1000 Genomes Project databases. The training pair comprises a total of 980 positive control (disease-causing) and 4,845 negative control (non-disease-causing) variants. The test pair consists of 1,959 positive and 9,691 negative controls.Results
CAROL has higher predictive power and accuracy for the effect of non-synonymous variants than each individual annotation tool (PolyPhen-2 and SIFT) and benefits from higher coverage.Conclusion
The combination of annotation tools can help improve automated prediction of whole-genome/exome non-synonymous variant functional consequences.
SUBMITTER: Lopes MC
PROVIDER: S-EPMC3390741 | biostudies-literature | 2012
REPOSITORIES: biostudies-literature
Lopes Margarida C MC Joyce Chris C Ritchie Graham R S GR John Sally L SL Cunningham Fiona F Asimit Jennifer J Zeggini Eleftheria E
Human heredity 20120118 1
<h4>Aims</h4>Next-generation sequencing has opened the possibility of large-scale sequence-based disease association studies. A major challenge in interpreting whole-exome data is predicting which of the discovered variants are deleterious or neutral. To address this question in silico, we have developed a score called Combined Annotation scoRing toOL (CAROL), which combines information from 2 bioinformatics tools: PolyPhen-2 and SIFT, in order to improve the prediction of the effect of non-syno ...[more]