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|Title:||Paralogue annotation identifies novel pathogenic variants in patients with brugada syndrome and catecholaminergic polymorphic ventricular tachycardia||Authors:||Walsh R.
|Issue Date:||2014||Publisher:||BMJ||Citation:||Walsh R., Peters N.S., Cook S.A., Ware J.S. (2014). Paralogue annotation identifies novel pathogenic variants in patients with brugada syndrome and catecholaminergic polymorphic ventricular tachycardia. Journal of Medical Genetics 51 (1) : 35-44. ScholarBank@NUS Repository. https://doi.org/10.1136/jmedgenet-2013-101917||Abstract:||Background Distinguishing genetic variants that cause disease from variants that are rare but benign is one of the principal challenges in contemporary clinical genetics, particularly as variants are identified at a pace exceeding the capacity of researchers to characterise them functionally. Methods We previously developed a novel method, called paralogue annotation, which accurately and specifically identifies disease-causing missense variants by transferring disease-causing annotations across families of related proteins. Here we refine our approach, and apply it to novel variants found in 2266 patients across two large cohorts with inherited sudden death syndromes, namely catecholaminergic polymorphic ventricular tachycardia (CPVT) or Brugada syndrome (BrS).Results Over one third of the novel non-synonymous variants found in these studies, which would otherwise be reported in a clinical diagnostics setting as 'variants of unknown significance', are categorised by our method as likely disease causing (positive predictive value 98.7%).This identified more than 500 new disease loci for BrS and CPVT. Conclusions Our methodology is widely transferable across all human disease genes, with an estimated 150 000 potentially informative annotations in more than 1800 genes. We have developed a web resource that allows researchers and clinicians to annotate variants found in individuals with inherited arrhythmias, comprising a referenced compendium of known missense variants in these genes together with a user-friendly implementation of our approach. This tool will facilitate the interpretation of many novel variants that might otherwise remain unclassified.||Source Title:||Journal of Medical Genetics||URI:||http://scholarbank.nus.edu.sg/handle/10635/149254||ISSN:||222593||DOI:||10.1136/jmedgenet-2013-101917|
|Appears in Collections:||Staff Publications|
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