Detecting gene duplications in the human lineage

Itan, Y., Bryson, K. and Thomas, M. G. (2010) Detecting gene duplications in the human lineage. Annals of Human Genetics, 74(6), pp. 555-565. (doi: 10.1111/j.1469-1809.2010.00609.x) (PMID:20946257)

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Abstract

Gene duplications represent an important class of evolutionary events that is likely to have contributed to the unique human phenotype in the short evolutionary time since the human-chimpanzee divergence. With the availability of both human and chimpanzee genome drafts in high coverage re-sequencing assemblies and the high annotation quality of most human genes, it should now be possible to identify all human lineage-specific gene duplication events (human inparalogues) and a few pioneering studies have attempted to do that. However, the different levels of coverage in the human and chimpanzee's genomes assemblies, and the differing levels of gene annotation, have led to problematic assumptions and oversimplifications in the algorithms and the datasets used to detect human lineage-specific gene duplications. In this study, we have developed a set of bioinformatic tools to overcome a number of the conceptual problems that are prevalent in previous studies and have collected a reliable and representative set of human inparalogues.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Bryson, Dr Kevin
Authors: Itan, Y., Bryson, K., and Thomas, M. G.
College/School:College of Science and Engineering > School of Computing Science
Journal Name:Annals of Human Genetics
Publisher:Wiley
ISSN:0003-4800
ISSN (Online):1469-1809
Published Online:14 October 2010

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