Bioinformatics Advance Access originally published online on September 3, 2004
Bioinformatics 2005 21(3):405-407; doi:10.1093/bioinformatics/bti009
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Bioinformatics vol. 21 issue 3 © Oxford University Press 2005; all rights reserved.
easyLINKAGE: a PERL script for easy and automated two-/multi-point linkage analyses
1 Division of Nephrology, Department of Medicine, Medical University Clinic at the University of Würzburg Würzburg, Germany
2 Department of Clinical Biochemistry and Pathobiochemistry, Medical University Clinic at the University of Würzburg Würzburg, Germany
3 Institute of Medical Genetics, Charité, Humboldt University Berlin Augustenburger Platz 1, 13353 Berlin, Germany
*To whom correspondence should be addressed.
Summary: We have generated the program easyLINKAGE that combines automated setup and performance of linkage analyses and simulation under an easy to handle graphical user interface for Microsoft Windows 2000/XP and standard UNIX systems. The program package supports two-point linkage analyses (FastLink v4.1 and SPLink v1.09), multi-point linkage analyses [GENEHUNTER v2.1, GENEHUNTER-PLUS with the emendation by Kong and Cox v1.2 (allele sharing modelling)] and the simulation package SLINK v2.65, and provides genome-wide as well as chromosomal postscript plots of LOD scores, NPL scores, P-values and other parameters.
Availability: http://www.uni-wuerzburg.de/nephrologie/molecular_genetics/molecular_genetics.htm
Contact: tom.lindner{at}mail.uni-wuerzburg.de
Supplementary information: Supplementary information is available on the website.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
R. Schule, M. Bonin, A. Durr, S. Forlani, A. D. Sperfeld, S. Klimpe, J. C. Mueller, A. Seibel, B. P. van de Warrenburg, P. Bauer, et al. Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24 Neurology, June 2, 2009; 72(22): 1893 - 1898. [Abstract] [Full Text] [PDF] |
||||
![]() |
N Hilgert, K Kahrizi, N Dieltjens, N Bazazzadegan, H Najmabadi, R J H Smith, and G Van Camp A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian family J. Med. Genet., April 1, 2009; 46(4): 272 - 276. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. M. Cavaco, P. F. Batista, L. G. Sobrinho, and V. Leite Mapping a New Familial Thyroid Epithelial Neoplasia Susceptibility Locus to Chromosome 8p23.1-p22 by High-Density Single-Nucleotide Polymorphism Genome-Wide Linkage Analysis J. Clin. Endocrinol. Metab., November 1, 2008; 93(11): 4426 - 4430. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. A. Ugur and A. Tolun Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation Hum. Mol. Genet., September 1, 2008; 17(17): 2644 - 2653. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. M Cavaco, P. F Batista, C. Martins, A. Banito, F. do Rosario, E. Limbert, L. G Sobrinho, and V. Leite Familial non-medullary thyroid carcinoma (FNMTC): analysis of fPTC/PRN, NMTC1, MNG1 and TCO susceptibility loci and identification of somatic BRAF and RAS mutations Endocr. Relat. Cancer, March 1, 2008; 15(1): 207 - 215. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Kyndt, J.-P. Gueffet, V. Probst, P. Jaafar, A. Legendre, F. Le Bouffant, C. Toquet, E. Roy, L. McGregor, S. A. Lynch, et al. Mutations in the Gene Encoding Filamin A as a Cause for Familial Cardiac Valvular Dystrophy Circulation, January 2, 2007; 115(1): 40 - 49. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Hoffmann and T. H. Lindner easyLINKAGE-Plus--automated linkage analyses using large-scale SNP data Bioinformatics, September 1, 2005; 21(17): 3565 - 3567. [Abstract] [Full Text] [PDF] |
||||






