Literature DB >> 15491493

GeneLink: a database to facilitate genetic studies of complex traits.

Elizabeth M Gillanders1, Anthony Masiello, Derek Gildea, Lowell Umayam, Priya Duggal, Mary Pat Jones, Alison P Klein, Diana Freas-Lutz, Grace Ibay, Ken Trout, Tyra G Wolfsberg, Jeffrey M Trent, Joan E Bailey-Wilson, Andreas D Baxevanis.   

Abstract

BACKGROUND: In contrast to gene-mapping studies of simple Mendelian disorders, genetic analyses of complex traits are far more challenging, and high quality data management systems are often critical to the success of these projects. To minimize the difficulties inherent in complex trait studies, we have developed GeneLink, a Web-accessible, password-protected Sybase database.
RESULTS: GeneLink is a powerful tool for complex trait mapping, enabling genotypic data to be easily merged with pedigree and extensive phenotypic data. Specifically designed to facilitate large-scale (multi-center) genetic linkage or association studies, GeneLink securely and efficiently handles large amounts of data and provides additional features to facilitate data analysis by existing software packages and quality control. These include the ability to download chromosome-specific data files containing marker data in map order in various formats appropriate for downstream analyses (e.g., GAS and LINKAGE). Furthermore, an unlimited number of phenotypes (either qualitative or quantitative) can be stored and analyzed. Finally, GeneLink generates several quality assurance reports, including genotyping success rates of specified DNA samples or success and heterozygosity rates for specified markers.
CONCLUSIONS: GeneLink has already proven an invaluable tool for complex trait mapping studies and is discussed primarily in the context of our large, multi-center study of hereditary prostate cancer (HPC). GeneLink is freely available at http://research.nhgri.nih.gov/genelink.

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Year:  2004        PMID: 15491493      PMCID: PMC526767          DOI: 10.1186/1471-2164-5-81

Source DB:  PubMed          Journal:  BMC Genomics        ISSN: 1471-2164            Impact factor:   3.969


  16 in total

1.  Toward high-throughput genotyping: dynamic and automatic software for manipulating large-scale genotype data using fluorescently labeled dinucleotide markers.

Authors:  J L Li; H Deng; D B Lai; F Xu; J Chen; G Gao; R R Recker; H W Deng
Journal:  Genome Res       Date:  2001-07       Impact factor: 9.043

2.  Genome-wide scan of Swedish families with hereditary prostate cancer: suggestive evidence of linkage at 5q11.2 and 19p13.3.

Authors:  Fredrik Wiklund; Elizabeth M Gillanders; Julie A Albertus; Anders Bergh; Jan-Erik Damber; Monica Emanuelsson; Diana L Freas-Lutz; Derek E Gildea; Ingela Göransson; MaryPat S Jones; Björn-Anders Jonsson; Fredrik Lindmark; Carol J Markey; Erica L Riedesel; Elisabeth Stenman; Jeffry M Trent; Henrik Grönberg
Journal:  Prostate       Date:  2003-12-01       Impact factor: 4.104

3.  Genome-wide scan for prostate cancer susceptibility genes using families from the University of Michigan prostate cancer genetics project finds evidence for linkage on chromosome 17 near BRCA1.

Authors:  Ethan M Lange; Elizabeth M Gillanders; Cralen C Davis; W Mark Brown; Joel K Campbell; MaryPat Jones; Derek Gildea; Erica Riedesel; Julie Albertus; Diana Freas-Lutz; Carol Markey; Veda Giri; Jennifer Beebe Dimmer; James E Montie; Jeffrey M Trent; Kathleen A Cooney
Journal:  Prostate       Date:  2003-12-01       Impact factor: 4.104

4.  Genome-wide scan for prostate cancer susceptibility genes in the Johns Hopkins hereditary prostate cancer families.

Authors:  Jianfeng Xu; Elizabeth M Gillanders; Sarah D Isaacs; Bao-Li Chang; Kathy E Wiley; S Lilly Zheng; MaryPat Jones; Derek Gildea; Erica Riedesel; Julie Albertus; Diana Freas-Lutz; Carol Markey; Deborah A Meyers; Patrick C Walsh; Jeffrey M Trent; William B Isaacs
Journal:  Prostate       Date:  2003-12-01       Impact factor: 4.104

5.  Germline mutations in the ribonuclease L gene in families showing linkage with HPC1.

Authors:  J Carpten; N Nupponen; S Isaacs; R Sood; C Robbins; J Xu; M Faruque; T Moses; C Ewing; E Gillanders; P Hu; P Bujnovszky; I Makalowska; A Baffoe-Bonnie; D Faith; J Smith; D Stephan; K Wiley; M Brownstein; D Gildea; B Kelly; R Jenkins; G Hostetter; M Matikainen; J Schleutker; K Klinger; T Connors; Y Xiang; Z Wang; A De Marzo; N Papadopoulos; O-P Kallioniemi; R Burk; D Meyers; H Grönberg; P Meltzer; R Silverman; J Bailey-Wilson; P Walsh; W Isaacs; J Trent
Journal:  Nat Genet       Date:  2002-01-22       Impact factor: 38.330

6.  A candidate prostate cancer susceptibility gene at chromosome 17p.

Authors:  S V Tavtigian; J Simard; D H Teng; V Abtin; M Baumgard; A Beck; N J Camp; A R Carillo; Y Chen; P Dayananth; M Desrochers; M Dumont; J M Farnham; D Frank; C Frye; S Ghaffari; J S Gupte; R Hu; D Iliev; T Janecki; E N Kort; K E Laity; A Leavitt; G Leblanc; J McArthur-Morrison; A Pederson; B Penn; K T Peterson; J E Reid; S Richards; M Schroeder; R Smith; S C Snyder; B Swedlund; J Swensen; A Thomas; M Tranchant; A M Woodland; F Labrie; M H Skolnick; S Neuhausen; J Rommens; L A Cannon-Albright
Journal:  Nat Genet       Date:  2001-02       Impact factor: 38.330

Review 7.  Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease.

Authors:  David Botstein; Neil Risch
Journal:  Nat Genet       Date:  2003-03       Impact factor: 38.330

8.  Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk.

Authors:  Jianfeng Xu; S Lilly Zheng; Akira Komiya; Josyf C Mychaleckyj; Sarah D Isaacs; Jennifer J Hu; David Sterling; Ethan M Lange; Gregory A Hawkins; Aubrey Turner; Charles M Ewing; Dennis A Faith; Jill R Johnson; Hiroyoshi Suzuki; Piroska Bujnovszky; Kathleen E Wiley; Angelo M DeMarzo; G Steven Bova; Baoli Chang; M Craig Hall; David L McCullough; Alan W Partin; Vahan S Kassabian; John D Carpten; Joan E Bailey-Wilson; Jeffrey M Trent; Jill Ohar; Eugene R Bleecker; Patrick C Walsh; William B Isaacs; Deborah A Meyers
Journal:  Nat Genet       Date:  2002-09-16       Impact factor: 38.330

9.  HGDBMS: a human genetics database management system.

Authors:  S A Seuchter; M H Skolnick
Journal:  Comput Biomed Res       Date:  1988-10

10.  Genome-wide scan for linkage in finnish hereditary prostate cancer (HPC) families identifies novel susceptibility loci at 11q14 and 3p25-26.

Authors:  Johanna Schleutker; Agnes B Baffoe-Bonnie; Elizabeth Gillanders; Tommi Kainu; Mary-Pat Jones; Diana Freas-Lutz; Carol Markey; Derek Gildea; Erica Riedesel; Julie Albertus; Kenneth D Gibbs; Mika Matikainen; Pasi A Koivisto; Teuvo Tammela; Joan E Bailey-Wilson; Jeffrey M Trent; Olli-P Kallioniemi
Journal:  Prostate       Date:  2003-12-01       Impact factor: 4.104

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  4 in total

1.  Identification of novel genetic loci for intraocular pressure: a genomewide scan of the Beaver Dam Eye Study.

Authors:  Priya Duggal; Alison P Klein; Kristine E Lee; Ronald Klein; Barbara E K Klein; Joan E Bailey-Wilson
Journal:  Arch Ophthalmol       Date:  2007-01

2.  The BiolAD-DB system : an informatics system for clinical and genetic data.

Authors:  David A Nielsen; Marty Leidner; Chad Haynes; Michael Krauthammer; Mary Jeanne Kreek
Journal:  Mol Diagn Ther       Date:  2007       Impact factor: 4.074

3.  dbVOR: a database system for importing pedigree, phenotype and genotype data and exporting selected subsets.

Authors:  Robert V Baron; Yvette P Conley; Michael B Gorin; Daniel E Weeks
Journal:  BMC Bioinformatics       Date:  2015-03-18       Impact factor: 3.169

4.  Mega2: validated data-reformatting for linkage and association analyses.

Authors:  Robert V Baron; Charles Kollar; Nandita Mukhopadhyay; Daniel E Weeks
Journal:  Source Code Biol Med       Date:  2014-12-05
  4 in total

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