Literature DB >> 12169547

Exact genetic linkage computations for general pedigrees.

M Fishelson1, D Geiger.   

Abstract

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.

Mesh:

Year:  2002        PMID: 12169547     DOI: 10.1093/bioinformatics/18.suppl_1.s189

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  96 in total

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2.  Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity.

Authors:  L Basel-Vanagaite; A Alkelai; R Straussberg; N Magal; D Inbar; M Mahajna; M Shohat
Journal:  J Med Genet       Date:  2003-10       Impact factor: 6.318

3.  A two-stage approximation for analysis of mixture genetic models in large pedigrees.

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Journal:  Genetics       Date:  2010-04-09       Impact factor: 4.562

4.  SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic system.

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Journal:  Am J Hum Genet       Date:  2010-10-28       Impact factor: 11.025

5.  A novel Markov chain monte carlo approach for constructing accurate meiotic maps.

Authors:  Andrew W George
Journal:  Genetics       Date:  2005-06-18       Impact factor: 4.562

6.  Online system for faster multipoint linkage analysis via parallel execution on thousands of personal computers.

Authors:  M Silberstein; A Tzemach; N Dovgolevsky; M Fishelson; A Schuster; D Geiger
Journal:  Am J Hum Genet       Date:  2006-05-01       Impact factor: 11.025

7.  Symptom dimensions as alternative phenotypes to address genetic heterogeneity in schizophrenia and bipolar disorder.

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Authors:  Ludovica Volpi; Gaia Roversi; Elisa Adele Colombo; Nico Leijsten; Daniela Concolino; Andrea Calabria; Maria Antonietta Mencarelli; Michele Fimiani; Fabio Macciardi; Rolph Pfundt; Eric F P M Schoenmakers; Lidia Larizza
Journal:  Am J Hum Genet       Date:  2009-12-10       Impact factor: 11.025

10.  Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation.

Authors:  Ofer Sarig; Sagi Nahum; Debora Rapaport; Akemi Ishida-Yamamoto; Dana Fuchs-Telem; Li Qiaoli; Ksenya Cohen-Katsenelson; Ronen Spiegel; Janna Nousbeck; Shirli Israeli; Zvi-Uri Borochowitz; Gilly Padalon-Brauch; Jouni Uitto; Mia Horowitz; Stavit Shalev; Eli Sprecher
Journal:  Am J Hum Genet       Date:  2012-07-26       Impact factor: 11.025

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