Literature DB >> 11731797

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees.

Gonçalo R Abecasis1, Stacey S Cherny, William O Cookson, Lon R Cardon.   

Abstract

Efforts to find disease genes using high-density single-nucleotide polymorphism (SNP) maps will produce data sets that exceed the limitations of current computational tools. Here we describe a new, efficient method for the analysis of dense genetic maps in pedigree data that provides extremely fast solutions to common problems such as allele-sharing analyses and haplotyping. We show that sparse binary trees represent patterns of gene flow in general pedigrees in a parsimonious manner, and derive a family of related algorithms for pedigree traversal. With these trees, exact likelihood calculations can be carried out efficiently for single markers or for multiple linked markers. Using an approximate multipoint calculation that ignores the unlikely possibility of a large number of recombinants further improves speed and provides accurate solutions in dense maps with thousands of markers. Our multipoint engine for rapid likelihood inference (Merlin) is a computer program that uses sparse inheritance trees for pedigree analysis; it performs rapid haplotyping, genotype error detection and affected pair linkage analyses and can handle more markers than other pedigree analysis packages.

Mesh:

Year:  2001        PMID: 11731797     DOI: 10.1038/ng786

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  1657 in total

1.  Evidence for linkage and association with reading disability on 6p21.3-22.

Authors:  D E Kaplan; J Gayán; J Ahn; T-W Won; D Pauls; R K Olson; J C DeFries; F Wood; B F Pennington; G P Page; S D Smith; J R Gruen
Journal:  Am J Hum Genet       Date:  2002-04-10       Impact factor: 11.025

2.  PowerTrim: An automated decision support algorithm for preprocessing family-based genetic data.

Authors:  Tricia A Thornton; Jonathan L Haines
Journal:  Am J Hum Genet       Date:  2003-04-03       Impact factor: 11.025

3.  Linkage analysis of extremely discordant and concordant sibling pairs identifies quantitative-trait loci that influence variation in the human personality trait neuroticism.

Authors:  Jan Fullerton; Matthew Cubin; Hemant Tiwari; Chenxi Wang; Amarjit Bomhra; Stuart Davidson; Sue Miller; Christopher Fairburn; Guy Goodwin; Michael C Neale; Simon Fiddy; Richard Mott; David B Allison; Jonathan Flint
Journal:  Am J Hum Genet       Date:  2003-02-20       Impact factor: 11.025

4.  HapScope: a software system for automated and visual analysis of functionally annotated haplotypes.

Authors:  Jinghui Zhang; William L Rowe; Jeffery P Struewing; Kenneth H Buetow
Journal:  Nucleic Acids Res       Date:  2002-12-01       Impact factor: 16.971

5.  Whole-Exome Sequencing Identifies the 6q12-q16 Linkage Region and a Candidate Gene, TTK, for Pulmonary Nontuberculous Mycobacterial Disease.

Authors:  Fei Chen; Eva P Szymanski; Kenneth N Olivier; Xinyue Liu; Hervé Tettelin; Steven M Holland; Priya Duggal
Journal:  Am J Respir Crit Care Med       Date:  2017-12-15       Impact factor: 21.405

6.  Robust relationship inference in genome-wide association studies.

Authors:  Ani Manichaikul; Josyf C Mychaleckyj; Stephen S Rich; Kathy Daly; Michèle Sale; Wei-Min Chen
Journal:  Bioinformatics       Date:  2010-10-05       Impact factor: 6.937

7.  Association of synapsin 2 with schizophrenia in families of Northern European ancestry.

Authors:  Viatcheslav Saviouk; Michael P Moreau; Irina V Tereshchenko; Linda M Brzustowicz
Journal:  Schizophr Res       Date:  2007-09-04       Impact factor: 4.939

8.  Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defects.

Authors:  Maria Arélin; Bernt Schulze; Bertram Müller-Myhsok; Denise Horn; Alexander Diers; Birgit Uhlenberg; Peter Nürnberg; Gudrun Nürnberg; Christian Becker; Stefan Mundlos; Tom H Lindner; Karl Sperling; Katrin Hoffmann
Journal:  Eur J Hum Genet       Date:  2012-10-03       Impact factor: 4.246

9.  The robustness of generalized estimating equations for association tests in extended family data.

Authors:  Bhoom Suktitipat; Rasika A Mathias; Dhananjay Vaidya; Lisa R Yanek; J Hunter Young; Lewis C Becker; Diane M Becker; Alexander F Wilson; M Daniele Fallin
Journal:  Hum Hered       Date:  2012-10-03       Impact factor: 0.444

Review 10.  Haplotyping methods for pedigrees.

Authors:  Guimin Gao; David B Allison; Ina Hoeschele
Journal:  Hum Hered       Date:  2009-01-27       Impact factor: 0.444

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