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Addressing False Positive Variants Arising from Pseudogenes
EP23700
Poster Title: Addressing False Positive Variants Arising from Pseudogenes
Submitted on 23 Dec 2015
Author(s): Risha Govind1,2, Sam Wilkinson1,3, Nicola Whiffin1,2, Shibu John1,2, Rachel J. Buchan1,2, Elizabeth Edwards1,2, Deborah J. Morris-Rosendahl1,3, James S. Ware1,2, P.J. Barton1,2, Stuart A. Cook1,2
Affiliations: 1National Heart and Lung Institute, Imperial College, London, UK, 2NIHR Cardiovascular BRU, Royal Brompton and Harefield NHS Trust, London, UK, 3Royal Brompton and Harefield NHS Trust, London, UK.
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Poster Information
Abstract: Clinical genetic testing has been transformed in recent years by the introduction of Next-Generation Sequencing (NGS). Targeted gene panels have made it possible to simultaneously analyse hundreds of genes with high confidence. However, since current aligners lack the sensitivity to distinguish reads that come from homologous parts of the genome, it is a challenge to work with genes with paralogues or pseudogenes. Pseudogenes arise from duplication of protein-coding genes, and have been considered to be degraded paralogues, due to loss of functionality. Summary: Clinical genetic testing has been transformed in recent years by the introduction of Next-Generation Sequencing (NGS). Report abuse »
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