Fokkema Ivo F A C, den Dunnen Johan T, Taschner Peter E M
Center of Human and Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.
Hum Mutat. 2005 Aug;26(2):63-8. doi: 10.1002/humu.20201.
The completion of the human genome project has initiated, as well as provided the basis for, the collection and study of all sequence variation between individuals. Direct access to up-to-date information on sequence variation is currently provided most efficiently through web-based, gene-centered, locus-specific databases (LSDBs). We have developed the Leiden Open (source) Variation Database (LOVD) software approaching the "LSDB-in-a-Box" idea for the easy creation and maintenance of a fully web-based gene sequence variation database. LOVD is platform-independent and uses PHP and MySQL open source software only. The basic gene-centered and modular design of the database follows the recommendations of the Human Genome Variation Society (HGVS) and focuses on the collection and display of DNA sequence variations. With minimal effort, the LOVD platform is extendable with clinical data. The open set-up should both facilitate and promote functional extension with scripts written by the community. The LOVD software is freely available from the Leiden Muscular Dystrophy pages (www.DMD.nl/LOVD/). To promote the use of LOVD, we currently offer curators the possibility to set up an LSDB on our Leiden server.
人类基因组计划的完成开启了对个体间所有序列变异的收集与研究,并为之提供了基础。目前,通过基于网络的、以基因为中心的位点特异性数据库(LSDBs)能最有效地直接获取有关序列变异的最新信息。我们开发了莱顿开放(源)变异数据库(LOVD)软件,它体现了“盒中LSDB”的理念,便于轻松创建和维护一个完全基于网络的基因序列变异数据库。LOVD与平台无关,仅使用PHP和MySQL开源软件。该数据库以基因为中心的基本模块化设计遵循了人类基因组变异协会(HGVS)的建议,专注于DNA序列变异的收集与展示。只需付出最小的努力,LOVD平台就能扩展临床数据。这种开放的设置应便于并促进社区编写的脚本进行功能扩展。LOVD软件可从莱顿肌营养不良症网页(www.DMD.nl/LOVD/)免费获取。为了推广LOVD的使用,我们目前为管理员提供了在我们莱顿服务器上建立一个LSDB的可能性。