Patrinos George P, van Baal Sjozef, Petersen Michael B, Papadakis Manoussos N
Erasmus University Medical Center, Faculty of Medicine and Health Sciences, MGC-Department of Cell Biology and Genetics, Rotterdam, The Netherlands.
Hum Mutat. 2005 Apr;25(4):327-33. doi: 10.1002/humu.20157.
The exponential discovery rate of new genomic alterations, leading to inherited disorders, as well as the need for comparative studies of different population's mutation frequencies necessitates recording their population-wide spectrum in online mutation databases. We report the construction of the Hellenic National Mutation database (http://www.goldenhelix.org/hellenic), a prototype database derived from a multicenter academic initiative, aiming to provide high quality and up-to-date information on the underlying genetic heterogeneity of inherited disorders found in the Hellenic population. Database records include informative summaries of the various genetic disorders studied in the Hellenic population, focused in particular on their incidence in Greece, a comprehensive reference list, and a well-structured query interface, which provides easy access to the list of the different mutations responsible for the inherited disorders in the Hellenic population. Also, extensive links to the respective Online Mendelian Inheritance in Man (OMIM) entries and, when available, to the locus-specific databases are provided, so that the user can retrieve the maximum amount of information from a single website. Furthermore, the Hellenic National Mutation database design allows easy data entry and curation. Creation of the Hellenic National Mutation database will significantly facilitate molecular diagnosis of inherited disorders in Greece and will motivate further investigation of yet unknown genetic diseases in the Hellenic population.
新的基因组改变导致遗传性疾病的指数级发现率,以及对不同人群突变频率进行比较研究的需求,使得有必要在在线突变数据库中记录其全人群范围的频谱。我们报告了希腊国家突变数据库(http://www.goldenhelix.org/hellenic)的构建,这是一个源自多中心学术倡议的原型数据库,旨在提供有关希腊人群中遗传性疾病潜在遗传异质性的高质量和最新信息。数据库记录包括对希腊人群中研究的各种遗传疾病的信息性总结,特别关注其在希腊的发病率、全面的参考文献列表以及结构良好的查询界面,该界面可方便地访问导致希腊人群遗传性疾病的不同突变列表。此外,还提供了与相应的《人类孟德尔遗传在线》(OMIM)条目以及特定基因座数据库(如有)的广泛链接,以便用户可以从单个网站检索最大量的信息。此外,希腊国家突变数据库的设计便于数据录入和管理。希腊国家突变数据库的创建将极大地促进希腊遗传性疾病的分子诊断,并将推动对希腊人群中尚未知晓的遗传疾病的进一步研究。