Literature DB >> 19582786

Assessment of SNP streak statistics using gene drop simulation with linkage disequilibrium.

Alun Thomas1.   

Abstract

We describe methods and programs for simulating the genotypes of individuals in a pedigree at large numbers of linked loci when the alleles of the founders are under linkage disequilibrium. Both simulation and estimation of linkage disequilibrium models are shown to be feasible on a genome wide scale. The methods are applied to evaluate the statistical significance of streaks of loci at which sets of related individuals share a common allele. The effects of properly allowing for linkage disequilibrium are shown to be important as they explain many of the large observations. This is illustrated by reanalysis of a previously reported linkage of prostate cancer to chromosome 1p23. 2009 Wiley-Liss, Inc.

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Year:  2010        PMID: 19582786      PMCID: PMC2811755          DOI: 10.1002/gepi.20440

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  22 in total

1.  Use of closely related affected individuals for the genetic study of complex diseases in founder populations.

Authors:  C Bourgain; E Génin; P Holopainen; K Mustalahti; M Mäki; J Partanen; F Clerget-Darpoux
Journal:  Am J Hum Genet       Date:  2000-11-30       Impact factor: 11.025

2.  Quantitative-trait homozygosity and association mapping and empirical genomewide significance in large, complex pedigrees: fasting serum-insulin level in the Hutterites.

Authors:  Mark Abney; Carole Ober; Mary Sara McPeek
Journal:  Am J Hum Genet       Date:  2002-03-04       Impact factor: 11.025

3.  Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses: ELAC2 and familial early-onset prostate cancer.

Authors:  Nicola J Camp; Jeff Swensen; Benjamin D Horne; James M Farnham; Alun Thomas; Lisa A Cannon-Albright; Sean V Tavtigian
Journal:  Genet Epidemiol       Date:  2005-04       Impact factor: 2.135

4.  Haplotype sharing analysis using mantel statistics.

Authors:  L Beckmann; D C Thomas; C Fischer; J Chang-Claude
Journal:  Hum Hered       Date:  2005-04-18       Impact factor: 0.444

5.  Homozygosity haplotype allows a genomewide search for the autosomal segments shared among patients.

Authors:  Hitoshi Miyazawa; Masaaki Kato; Takuya Awata; Masakazu Kohda; Hiroyasu Iwasa; Nobuyuki Koyama; Tomoaki Tanaka; Shunei Kyo; Yasushi Okazaki; Koichi Hagiwara
Journal:  Am J Hum Genet       Date:  2007-05-02       Impact factor: 11.025

6.  Towards linkage analysis with markers in linkage disequilibrium by graphical modelling.

Authors:  Alun Thomas
Journal:  Hum Hered       Date:  2007-04-27       Impact factor: 0.444

7.  Haplotype sharing analysis in affected individuals from nuclear families with at least one affected offspring.

Authors:  M A Van der Meulen; G J te Meerman
Journal:  Genet Epidemiol       Date:  1997       Impact factor: 2.135

8.  A novel approach to search for identity by descent in small samples of patients and controls from the same mendelian breeding unit: a pilot study on myopia.

Authors:  S Heath; R Robledo; W Beggs; G Feola; C Parodo; A Rinaldi; L Contu; D Dana; D Stambolian; M Siniscalco
Journal:  Hum Hered       Date:  2001       Impact factor: 0.444

9.  Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis.

Authors:  R H Houwen; S Baharloo; K Blankenship; P Raeymaekers; J Juyn; L A Sandkuijl; N B Freimer
Journal:  Nat Genet       Date:  1994-12       Impact factor: 38.330

10.  Comprehensive human genetic maps: individual and sex-specific variation in recombination.

Authors:  K W Broman; J C Murray; V C Sheffield; R L White; J L Weber
Journal:  Am J Hum Genet       Date:  1998-09       Impact factor: 11.025

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  11 in total

1.  A method for detecting IBD regions simultaneously in multiple individuals--with applications to disease genetics.

Authors:  Ida Moltke; Anders Albrechtsen; Thomas V O Hansen; Finn C Nielsen; Rasmus Nielsen
Journal:  Genome Res       Date:  2011-04-14       Impact factor: 9.043

2.  Obtaining accurate p values from a dense SNP linkage scan.

Authors:  William C L Stewart; Ryan L Subaran
Journal:  Hum Hered       Date:  2012-10-03       Impact factor: 0.444

3.  Family Study Designs Informed by Tumor Heterogeneity and Multi-Cancer Pleiotropies: The Power of the Utah Population Database.

Authors:  Heidi A Hanson; Claire L Leiser; Michael J Madsen; John Gardner; Stacey Knight; Melissa Cessna; Carol Sweeney; Jennifer A Doherty; Ken R Smith; Philip S Bernard; Nicola J Camp
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2020-02-25       Impact factor: 4.254

4.  Modelling and visualizing fine-scale linkage disequilibrium structure.

Authors:  David Edwards
Journal:  BMC Bioinformatics       Date:  2013-06-06       Impact factor: 3.169

5.  Employing MCMC under the PPL framework to analyze sequence data in large pedigrees.

Authors:  Yungui Huang; Alun Thomas; Veronica J Vieland
Journal:  Front Genet       Date:  2013-04-19       Impact factor: 4.599

6.  Pairwise shared genomic segment analysis in high-risk pedigrees: application to Genetic Analysis Workshop 17 exome-sequencing SNP data.

Authors:  Zheng Cai; Stacey Knight; Alun Thomas; Nicola J Camp
Journal:  BMC Proc       Date:  2011-11-29

7.  Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees.

Authors:  Zheng Cai; Alun Thomas; Craig Teerlink; James M Farnham; Lisa A Cannon-Albright; Nicola J Camp
Journal:  BMC Genomics       Date:  2012-11-28       Impact factor: 3.969

8.  Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21.

Authors:  Lisa A Cannon-Albright; Craig C Teerlink; James M Farnham; Alun W Thomas; John J Zone; Sancy A Leachman
Journal:  J Invest Dermatol       Date:  2012-09-06       Impact factor: 8.551

9.  CrypticIBDcheck: an R package for checking cryptic relatedness in nominally unrelated individuals.

Authors:  Annick Nembot-Simo; Jinko Graham; Brad McNeney
Journal:  Source Code Biol Med       Date:  2013-02-06

10.  Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene.

Authors:  Yukinori Okada; Dorothee Diogo; Jeffrey D Greenberg; Faten Mouassess; Walid A L Achkar; Robert S Fulton; Joshua C Denny; Namrata Gupta; Daniel Mirel; Stacy Gabriel; Gang Li; Joel M Kremer; Dimitrios A Pappas; Robert J Carroll; Anne E Eyler; Gosia Trynka; Eli A Stahl; Jing Cui; Richa Saxena; Marieke J H Coenen; Henk-Jan Guchelaar; Tom W J Huizinga; Philippe Dieudé; Xavier Mariette; Anne Barton; Helena Canhão; João E Fonseca; Niek de Vries; Paul P Tak; Larry W Moreland; S Louis Bridges; Corinne Miceli-Richard; Hyon K Choi; Yoichiro Kamatani; Pilar Galan; Mark Lathrop; Towfique Raj; Philip L De Jager; Soumya Raychaudhuri; Jane Worthington; Leonid Padyukov; Lars Klareskog; Katherine A Siminovitch; Peter K Gregersen; Elaine R Mardis; Thurayya Arayssi; Layla A Kazkaz; Robert M Plenge
Journal:  PLoS One       Date:  2014-02-10       Impact factor: 3.240

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