Literature DB >> 8013891

LABMAN and LINKMAN: a data management system specifically designed for genome searches of complex diseases.

P Adams1.   

Abstract

Two programs have been developed to manage linkage analysis data. The first program, LABMAN, is a comprehensive laboratory data management system organizing pedigrees, blood DNA samples, DNA markers, Southern blot or polyacrylamide gels, autoradiographs, and marker-allele typings generated from these samples. Output includes mendelization checks for genetic incompatibilities in typings and formatted files ready for linkage analysis. LABMAN can also compress highly polymorphic allele systems into smaller allele systems facilitating analysis of large systems. The second program, LINKMAN, provides data management for lod score output from linkage analyses. It reads linkage analysis output files, calculates lod scores by family, associates lod scores with specific marker and family identifiers, and stores these data in a database where they can be combined with lod scores from previous analyses. LINKMAN easily incorporates any of a wide variety of genetic models. It produces formatted output of lod scores by user-specified criteria for reports or as ASCII files for input to other programs. If desired, tests of homogeneity of linkage across families can be run via the HOMOG program [Ott, 1991] and their output included in reports. The programs include features critical for conducting genome searches of complex diseases: They are easy-to-use, well-tested, and reliable. Data from multicenter investigations can be easily combined for analysis. Moreover, they include extensive error-checking capabilities, and they are specifically set up to protect blindness between laboratory workers and data analysts. LABMAN and LINKMAN are currently available free of charge under DOS.

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Year:  1994        PMID: 8013891     DOI: 10.1002/gepi.1370110109

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  12 in total

1.  The gene for May-Hegglin anomaly localizes to a <1-Mb region on chromosome 22q12.3-13.1.

Authors:  J A Martignetti; K E Heath; J Harris; N Bizzaro; A Savoia; C L Balduini; R J Desnick
Journal:  Am J Hum Genet       Date:  2000-03-17       Impact factor: 11.025

2.  Genomewide linkage analysis of celiac disease in Finnish families.

Authors:  Jianjun Liu; Suh-Hang Juo; Päivi Holopainen; Joseph Terwilliger; Xiaomei Tong; Adina Grunn; Miguel Brito; Peter Green; Kirsi Mustalahti; Markku Mäki; T Conrad Gilliam; Jukka Partanen
Journal:  Am J Hum Genet       Date:  2001-11-19       Impact factor: 11.025

3.  Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata.

Authors:  Amalia Martinez-Mir; Abraham Zlotogorski; Derek Gordon; Lynn Petukhova; Jianhong Mo; T Conrad Gilliam; Douglas Londono; Chad Haynes; Jurg Ott; Maria Hordinsky; Krassimira Nanova; David Norris; Vera Price; Madeleine Duvic; Angela M Christiano
Journal:  Am J Hum Genet       Date:  2007-01-05       Impact factor: 11.025

4.  A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus.

Authors:  V M Aita; J Liu; J A Knowles; J D Terwilliger; R Baltazar; A Grunn; J E Loth; K Kanyas; B Lerer; J Endicott; Z Wang; G Penchaszadeh; T C Gilliam; M Baron
Journal:  Am J Hum Genet       Date:  1999-01       Impact factor: 11.025

Review 5.  Programs, databases, and expert systems for human geneticists--a survey.

Authors:  C Fischer; S Schweigert; C Spreckelsen; F Vogel
Journal:  Hum Genet       Date:  1996-02       Impact factor: 4.132

6.  Diaphyseal medullary stenosis with malignant fibrous histiocytoma: a hereditary bone dysplasia/cancer syndrome maps to 9p21-22.

Authors:  J A Martignetti; R J Desnick; E Aliprandis; K I Norton; P Hardcastle; S Nade; B D Gelb
Journal:  Am J Hum Genet       Date:  1999-03       Impact factor: 11.025

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

Authors:  Elizabeth M Gillanders; 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
Journal:  BMC Genomics       Date:  2004-10-18       Impact factor: 3.969

8.  Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q.

Authors:  Haiyan Xu; Rong Cheng; Suh-Hang Juo; Jianjun Liu; Jo Ellen Loth; Jean Endicott; Conrad Gilliam; Miron Baron
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2010-12-16       Impact factor: 3.568

9.  Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean Hispanics.

Authors:  J H Lee; R Mayeux; D Mayo; J Mo; V Santana; J Williamson; A Flaquer; A Ciappa; H Rondon; P Estevez; R Lantigua; T Kawarai; A Toulina; M Medrano; M Torres; Y Stern; B Tycko; E Rogaeva; P St George-Hyslop; J A Knowles
Journal:  Mol Psychiatry       Date:  2004-11       Impact factor: 15.992

10.  A genomewide screen of 345 families for autism-susceptibility loci.

Authors:  Amanda L Yonan; Maricela Alarcón; Rong Cheng; Patrik K E Magnusson; Sarah J Spence; Abraham A Palmer; Adina Grunn; Suh-Hang Hank Juo; Joseph D Terwilliger; Jianjun Liu; Rita M Cantor; Daniel H Geschwind; T Conrad Gilliam
Journal:  Am J Hum Genet       Date:  2003-09-17       Impact factor: 11.025

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