GeneSeeker: extraction and integration of human disease-related information from web-based genetic databases

被引:56
作者
van Driel, MA
Cuelenaere, K
Kemmeren, PPCW
Leunissen, JAM
Brunner, HG
Vriend, G
机构
[1] Radboud Univ Nijmegen, Ctr Mol & Biomol Informat, NL-6500 GL Nijmegen, Netherlands
[2] Dalicon BV, NL-6700 AJ Wageningen, Netherlands
[3] Univ Utrecht, Med Ctr, Genom Lab, NL-3508 AB Utrecht, Netherlands
[4] Univ Wageningen & Res Ctr, Wageningen, Netherlands
[5] Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
关键词
D O I
10.1093/nar/gki435
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The identification of genes underlying human genetic disorders requires the combination of data related to cytogenetic localization, phenotypes and expression patterns, to generate a list of candidate genes. In the field of human genetics, it is normal to perform this combination analysis by hand. We report on GeneSeeker (http://www.cmbi.ru.nl/GeneSeeker/), a web server that gathers and combines data from a series of databases. All database searches are performed via the web interfaces provided with the original databases, guaranteeing that the most recent data are queried, and obviating data warehousing. GeneSeeker makes the same selection of candidate genes as the human geneticists would have performed, and thus reducing the time-consuming process to a few minutes. GeneSeeker is particularly well suited for syndromes in which the disease gene displays altered expression patterns in the affected tissue(s).
引用
收藏
页码:W758 / W761
页数:4
相关论文
共 18 条
  • [1] Apweiler R, 2004, NUCLEIC ACIDS RES, V32, pD115, DOI [10.1093/nar/gkw1099, 10.1093/nar/gkh131]
  • [2] Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes
    Blackshaw, S
    Fraioli, RE
    Furukawa, T
    Cepko, CL
    [J]. CELL, 2001, 107 (05) : 579 - 589
  • [3] MGD: the Mouse Genome Database
    Blake, JA
    Richardson, JE
    Bult, RJ
    Kadin, JA
    Eppig, JT
    [J]. NUCLEIC ACIDS RESEARCH, 2003, 31 (01) : 193 - 195
  • [4] A chromosomal duplication map of malformations: Regions of suspected haplo- and triplolethality - and tolerance of segmental aneuploidy - in humans
    Brewer, C
    Holloway, S
    Zawalnyski, P
    Schinzel, A
    FitzPatrick, D
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (06) : 1702 - 1708
  • [5] A chromosomal deletion map of human malformations
    Brewer, C
    Holloway, S
    Zawalnyski, P
    Schinzel, A
    FitzPatrick, D
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (04) : 1153 - 1159
  • [6] Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)
    Chiang, AP
    Nishimura, D
    Searby, C
    Elbedour, K
    Carmi, R
    Ferguson, AL
    Secrist, J
    Braun, T
    Casavant, T
    Stone, EM
    Sheffield, VC
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 75 (03) : 475 - 484
  • [7] Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridization
    den Hollander, AI
    van Driel, MA
    de Kok, YJM
    van de Pol, DJR
    Hoyng, CB
    Brunner, HG
    Deutman, AF
    Cremers, FPM
    [J]. GENOMICS, 1999, 58 (03) : 240 - 249
  • [8] Gene-based approach to human gene-phenotype correlations
    Dryja, TP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (22) : 12117 - 12121
  • [9] THE OXFORD GRID
    EDWARDS, JH
    [J]. ANNALS OF HUMAN GENETICS, 1991, 55 : 17 - 31
  • [10] Etzold T, 1996, METHOD ENZYMOL, V266, P114