LOVD: Easy creation of a locus-specific sequence variation database using an "LSDB-in-a-Box" approach

被引:196
作者
Fokkema, IFAC [1 ]
den Dunnen, JT [1 ]
Taschner, PEM [1 ]
机构
[1] Leiden Univ, Ctr Med, Ctr Human & Clin Genet, NL-2300 RA Leiden, Netherlands
关键词
LSDB; database; open source; PHP; MySQL; mutation; LMNA; LOVD;
D O I
10.1002/humu.20201
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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 setup an LSDB on our Leiden server.
引用
收藏
页码:63 / 68
页数:6
相关论文
共 17 条
  • [1] Béroud C, 2000, HUM MUTAT, V15, P86, DOI 10.1002/(SICI)1098-1004(200001)15:1<86::AID-HUMU16>3.0.CO
  • [2] 2-4
  • [3] Brown AF, 2000, HUM MUTAT, V15, P76, DOI 10.1002/(SICI)1098-1004(200001)15:1<76::AID-HUMU15>3.0.CO
  • [4] 2-8
  • [5] Time for a unified system of mutation description and reporting: A review of locus-specific mutation Databases
    Claustres, M
    Horaitis, O
    Vanevski, M
    Cotton, RGH
    [J]. GENOME RESEARCH, 2002, 12 (05) : 680 - 688
  • [6] den Dunnen JT, 2000, HUM MUTAT, V15, P7
  • [7] HGVbase:: a curated resource describing human DNA variation and phenotype relationships
    Fredman, D
    Munns, G
    Rios, D
    Sjöholm, F
    Siegfried, M
    Lenhard, B
    Lehväslaiho, H
    Brookes, AJ
    [J]. NUCLEIC ACIDS RESEARCH, 2004, 32 : D516 - D519
  • [8] Hamosh A, 2005, NUCLEIC ACIDS RES, V33, pD514
  • [9] The challenge of documenting mutation across the genome: The human genome variation society approach
    Horaitis, O
    Cotton, RGH
    [J]. HUMAN MUTATION, 2004, 23 (05) : 447 - 452
  • [10] OHTSUBO M, 2003, GENOME INFORMATICS, P284