Literature DB >> 15780967

Human genome-wide screen of haplotype-like blocks of reduced diversity.

Javier Costas1, Antonio Salas, Christopher Phillips, Angel Carracedo.   

Abstract

An important proportion of the human genome is organized in regions of high linkage disequilibrium (LD) and low haplotype diversity, referred to as haplotype blocks. Here, we perform a genome-wide screen of haplotype-like blocks presenting just two main haplotypes at a frequency higher than 1%, based on single-nucleotide polymorphism (SNP) frequencies from two populations: African-Americans and Caucasians, using data from the Celera SNP database. These haplotype-like blocks of reduced diversity are more abundant and of longer size in Caucasians, in agreement with population history. Several of the discovered blocks are good candidates for targets of natural selection, such as those blocks containing a cluster of bitter taste receptors or the apolipoprotein L1. In addition, several genes putatively involved in susceptibility to common diseases are included in these haplotype-like blocks of reduced diversity. This fact may present important implications in association studies, leading to a reduction of genotyping efforts.

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Year:  2005        PMID: 15780967     DOI: 10.1016/j.gene.2004.12.042

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  6 in total

Review 1.  Evaluating HapMap SNP data transferability in a large-scale genotyping project involving 175 cancer-associated genes.

Authors:  Gloria Ribas; Anna González-Neira; Antonio Salas; Roger L Milne; Ana Vega; Begoña Carracedo; Emilio González; Eva Barroso; Lara P Fernández; Patricio Yankilevich; Mercedes Robledo; Angel Carracedo; Javier Benítez
Journal:  Hum Genet       Date:  2005-12-02       Impact factor: 4.132

Review 2.  Online resources for SNP analysis: a review and route map.

Authors:  Christopher Phillips
Journal:  Mol Biotechnol       Date:  2007-01       Impact factor: 2.695

3.  Linkage disequilibrium patterns and functional analysis of RGS4 polymorphisms in relation to schizophrenia.

Authors:  Kodavali V Chowdari; Mikhil Bamne; Joel Wood; Michael E Talkowski; Karoly Mirnics; Pat Levitt; David A Lewis; Vishwajit L Nimgaonkar
Journal:  Schizophr Bull       Date:  2007-05-21       Impact factor: 9.306

4.  MIDAS: software for analysis and visualisation of interallelic disequilibrium between multiallelic markers.

Authors:  Tom R Gaunt; Santiago Rodriguez; Carlos Zapata; Ian N M Day
Journal:  BMC Bioinformatics       Date:  2006-04-27       Impact factor: 3.169

5.  A genome-wide scan for breast cancer risk haplotypes among African American women.

Authors:  Chi Song; Gary K Chen; Robert C Millikan; Christine B Ambrosone; Esther M John; Leslie Bernstein; Wei Zheng; Jennifer J Hu; Regina G Ziegler; Sarah Nyante; Elisa V Bandera; Sue A Ingles; Michael F Press; Sandra L Deming; Jorge L Rodriguez-Gil; Stephen J Chanock; Peggy Wan; Xin Sheng; Loreall C Pooler; David J Van Den Berg; Loic Le Marchand; Laurence N Kolonel; Brian E Henderson; Chris A Haiman; Daniel O Stram
Journal:  PLoS One       Date:  2013-02-28       Impact factor: 3.240

6.  Contamination and sample mix-up can best explain some patterns of mtDNA instabilities in buccal cells and oral squamous cell carcinoma.

Authors:  Hans-Jürgen Bandelt; Antonio Salas
Journal:  BMC Cancer       Date:  2009-04-16       Impact factor: 4.430

  6 in total

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