Skip Navigation

This Article
Right arrow FREE Full Text (Print PDF) Freely available
Right arrow FREE Full Text (Screen PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Fishelson, M.
Right arrow Articles by Geiger, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fishelson, M.
Right arrow Articles by Geiger, D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Bioinformatics Vol. 18 no. 90001 2002
Pages S189-S198
© 2002 Oxford University Press

Exact genetic linkage computations for general pedigrees

M. Fishelson and D. Geiger

Computer Science Department, Technion, Haifa 32000, Israel

Received on January 24, 2002 ; revised on March 26, 2002 ; accepted on March 26, 2002

Motivation: Genetic linkage analysis is a useful statistical tool for mapping disease genes and for associating functionality of genes with their location on the chromosome. There is a need for a program that computes multipoint likelihood on general pedigrees with many markers that also deals with two-locus disease models.

Results: In this paper we present algorithms for performing exact multipoint likelihood calculations on general pedigrees with a large number of highly polymorphic markers, taking into account a variety of disease models. We have implemented these algorithms in a new computer program called SUPERLINK which outperforms leading linkage software with regards to functionality, speed, memory requirements and extensibility.

Availability: SUPERLINK is available at http://bioinfo.cs.technion.ac.il/superlink

Contact: fmaayan{at}cs.technion.ac.il dang{at}cs.technion.ac.il

Keywords: Bayesian networks; Fastlink; Genehunter; linkage analysis; Vitesse.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
GeneticsHome page
C. A. Albers, T. Heskes, and H. J. Kappen
Haplotype Inference in General Pedigrees Using the Cluster Variation Method
Genetics, October 1, 2007; 177(2): 1101 - 1116.
[Abstract] [Full Text] [PDF]


Home page
J HeredHome page
J. S. Kehler, V. A. David, A. A. Schaffer, K. Bajema, E. Eizirik, D. K. Ryugo, S. S. Hannah, S. J. O'Brien, and M. Menotti-Raymond
Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
J. Hered., September 1, 2007; 98(6): 555 - 566.
[Abstract] [Full Text] [PDF]


Home page
J HeredHome page
M. Menotti-Raymond, V. A. David, A. A. Schaffer, R. Stephens, D. Wells, R. Kumar-Singh, S. J. O'Brien, and K. Narfstrom
Mutation in CEP290 Discovered for Cat Model of Human Retinal Degeneration
J. Hered., May 16, 2007; (2007) esm019v1.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
D. Cohen, U. Bar-Yosef, J. Levy, L. Gradstein, N. Belfair, R. Ofir, S. Joshua, T. Lifshitz, R. Carmi, and O. S. Birk
Homozygous CRYBB1 Deletion Mutation Underlies Autosomal Recessive Congenital Cataract
Invest. Ophthalmol. Vis. Sci., May 1, 2007; 48(5): 2208 - 2213.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
J. Jung, G. Bohn, A. Allroth, K. Boztug, G. Brandes, I. Sandrock, A. A. Schaffer, C. Rathinam, I. Kollner, C. Beger, et al.
Identification of a homozygous deletion in the AP3B1 gene causing Hermansky-Pudlak syndrome, type 2
Blood, July 1, 2006; 108(1): 362 - 369.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
A. W. George
A Novel Markov Chain Monte Carlo Approach for Constructing Accurate Meiotic Maps
Genetics, October 1, 2005; 171(2): 791 - 801.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
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]


Home page
J. Med. Genet.Home page
J Ausseil, J C Loredo-Osti, A Verner, C Darmond-Zwaig, I Maire, B Poorthuis, O P van Diggelen, T J Hudson, T M Fujiwara, K Morgan, et al.
Localisation of a gene for mucopolysaccharidosis IIIC to the pericentromeric region of chromosome 8
J. Med. Genet., December 1, 2004; 41(12): 941 - 945.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
L. Basel-Vanagaite, R. Straussberg, H. Ovadia, A. Kaplan, N. Magal, Z. Shorer, H. Shalev, C. Walsh, and M. Shohat
Infantile bilateral striatal necrosis maps to chromosome 19q
Neurology, January 13, 2004; 62(1): 87 - 90.
[Abstract] [Full Text] [PDF]


Home page
J. Med. Genet.Home page
L Basel-Vanagaite, A Alkelai, R Straussberg, N Magal, D Inbar, M Mahajna, and M Shohat
Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity
J. Med. Genet., October 1, 2003; 40(10): 729 - 732.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.