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The challenge of documenting mutation across the genome: The human genome variation society approach
Author(s): Horaitis O, Cotton RGH
Source: HUMAN MUTATION    Volume: 23    Issue: 5    Pages: 447-452    Published: 2004  
Times Cited: 24     References: 22     
Abstract: New methods for the detection of mutations and the completion of the human genome sequencing project have contributed to an exponential rise in variation information that must be collected, quality controlled, documented, and stored safely to ensure future availability to health care professionals, researchers, and others. There may be anywhere from one to more than 1,000 mutations in any given gene. To date, this information has been collected by general databases such as Online Mendelian Inheritance in Man (OMIM) or the Human Gene Mutation Database (HGMD), which collect only published mutations and, in the case of OMIM, selected published mutations. Unpublished mutations have made their way into Locus Specific Databases (LSDBs), and these can often contain as many unpublished mutations as published ones, in addition to other more detailed gene-specific information. LSDBs, however, do not exist for all genes at this time. Through their interactions, a number of members of the Human Genome Variation Society (HGVS) have developed nomenclature, standard software to curate mutations in gene specific databases, a WayStation to collect and review new mutations from research and diagnostic laboratories, and central databases to store and display these mutations and their associated phenotypes. Nomenclature is now well defined for the commonest types of mutation, with work continuing on systematically naming the more complex types. Other projects, such as dedicated specialized software for LSDBs, are in the early stages of development. (C) 2004 Wiley Liss, Inc.
Document Type: Article
Language: English
Reprint Address: Cotton, RGH (reprint author), Genom Disorders Res Ctr, Level 2,161 Barry St, Carlton, Vic 3053 Australia
Addresses:
1. Genom Disorders Res Ctr, Melbourne, Vic Australia
2. Univ Melbourne, Dept Med, Melbourne, Vic Australia
Publisher: WILEY-LISS, DIV JOHN WILEY & SONS INC, 605 THIRD AVE, NEW YORK, NY 10158-0012 USA
Subject Category: Genetics & Heredity
IDS Number: 816OP
ISSN: 1059-7794
DOI: 10.1002/humu.20038
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