Literature DB >> 8112059

LODVIEW: a computer program for the graphical evaluation of lod score results in exclusion mapping of human disease genes.

F Hildebrandt1, A Pohlmann, H Omran.   

Abstract

For linkage analysis projects aimed at mapping hereditary disease genes in humans, hundreds of highly polymorphic microsatellite markers which can be typed by PCR (PCR markers) have become available. With this technical improvement, the availability of a technique allowing for transparency in the handling of rapidly generated lod score data is becoming important. We present a computer program LODVIEW for the graphical representation of lod score data. It is designed for the input of lod score data generated with the LINKAGE package or similar programs. LODVIEW consists of 24 preformatted files, one for each chromosome. Each file contains a table for the input of lod score data and a file for the graphical representation of the data, which will show automatically any entry that is made in the respective input table. The program provides the user with published PCR marker information pre-entered into a table and graph at the correct positions corresponding to the genetic distances between markers. The graphical display of LODVIEW allows for the rapid evaluation of lod score results calculated from PCR markers on each chromosome. The following information can be obtained from the graphical display at one glance: (i) Regions of exclusion (Z(theta) < -2) and nonexclusion, (ii) markers with positive lod scores, (iii) the distribution of positive and negative lod scores among the families examined (indication of genetic heterogeneity), (iv) multipoint lod scores, and (v) the availability of PCR markers in regions of interest. The program is continually updated for novel PCR marker information from the literature. The program will help to efficiently monitor and direct the progress of exclusion mapping projects.

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Year:  1993        PMID: 8112059     DOI: 10.1006/cbmr.1993.1042

Source DB:  PubMed          Journal:  Comput Biomed Res        ISSN: 0010-4809


  8 in total

1.  Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree.

Authors:  H Omran; C Fernandez; M Jung; K Häffner; B Fargier; A Villaquiran; R Waldherr; N Gretz; M Brandis; F Rüschendorf; A Reis; F Hildebrandt
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

2.  Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish population.

Authors:  A Fuchshuber; P Niaudet; O Gribouval; G Jean; M C Gubler; M Broyer; C Antignac
Journal:  Pediatr Nephrol       Date:  1996-04       Impact factor: 3.714

3.  Mapping of gene loci for nephronophthisis type 4 and Senior-Løken syndrome, to chromosome 1p36.

Authors:  Maria J Schuermann; Edgar Otto; Achim Becker; Katrin Saar; Franz Rüschendorf; Bettine C Polak; Sirpa Ala-Mello; Julia Hoefele; Alexander Wiedensohler; Maria Haller; Heymut Omran; Peter Nürnberg; Friedhelm Hildebrandt
Journal:  Am J Hum Genet       Date:  2002-03-27       Impact factor: 11.025

4.  Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22.

Authors:  M Jung; I Poepping; A Perrot; A E Ellmer; T F Wienker; R Dietz; A Reis; K J Osterziel
Journal:  Am J Hum Genet       Date:  1999-10       Impact factor: 11.025

5.  Gene localization for an autosomal dominant familial periodic fever to 12p13.

Authors:  J Mulley; K Saar; G Hewitt; F Rüschendorf; H Phillips; A Colley; D Sillence; A Reis; M Wilson
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

6.  High-resolution mapping of the gene for cystinosis, using combined biochemical and linkage analysis.

Authors:  G Jean; A Fuchshuber; M M Town; O Gribouval; J A Schneider; M Broyer; W van't Hoff; P Niaudet; C Antignac
Journal:  Am J Hum Genet       Date:  1996-03       Impact factor: 11.025

7.  The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster.

Authors:  M Vollmer; M Jung; F Rüschendorf; R Ruf; T Wienker; A Reis; R Krapf; F Hildebrandt
Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025

8.  Hereditary isolated renal magnesium loss maps to chromosome 11q23.

Authors:  I C Meij; K Saar; L P van den Heuvel; G Nuernberg; M Vollmer; F Hildebrandt; A Reis; L A Monnens; N V Knoers
Journal:  Am J Hum Genet       Date:  1999-01       Impact factor: 11.025

  8 in total

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