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Hum Mutat. 2012 Aug;33(8):1188-1191. doi: 10.1002/humu.22114. Epub 2012 Jun 7.

Paralogous annotation of disease-causing variants in long QT syndrome genes.

Author information

1
Medical Research Council Clinical Sciences Centre, Imperial College London, London W12 0NN, United Kingdom.
2
Cardiovascular Biomedical Research Unit, Royal Brompton & Harefield NHS Trust, London SW3 6NP, United Kingdom.
3
European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SD, United Kingdom.
#
Contributed equally

Abstract

Discriminating between rare benign and pathogenic variation is a key challenge in clinical genetics, particularly as increasing numbers of nonsynonymous single-nucleotide polymorphisms (SNPs) are identified in resequencing studies. Here, we describe an approach for the functional annotation of nonsynonymous variants that identifies functionally important, disease-causing residues across protein families using multiple sequence alignment. We applied the methodology to long QT syndrome (LQT) genes, which cause sudden death, and their paralogues, which largely cause neurological disease. This approach accurately classified known LQT disease-causing variants (positive predictive value = 98.4%) with a better performance than established bioinformatic methods. The analysis also identified 1078 new putative disease loci, which we incorporated along with known variants into a comprehensive and freely accessible long QT resource (http://cardiodb.org/Paralogue_Annotation/), based on newly created Locus Reference Genomic sequences (http://www.lrg-sequence.org/). We propose that paralogous annotation is widely applicable for Mendelian human disease genes.

PMID:
22581653
PMCID:
PMC4640174
DOI:
10.1002/humu.22114
[Indexed for MEDLINE]
Free PMC Article

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