Literature DB >> 12052145

How many SNPs does a genome-wide haplotype map require?

Richard Judson1, Benjamin Salisbury, Julie Schneider, Andreas Windemuth, J Claiborne Stephens.   

Abstract

We derive and compare several estimates of the number of SNPs that would be required to form the basis of a complete haplotype survey of the human genome. Our estimates make use of reports published by Stephens et al. [1], Patil et al. [2] and Daly et al. [3]. The estimated number of SNPs required for a genome-wide haplotype survey ranges from 180K (based on a European sample of 16 chromosomes) to 600K (based on an ethnically diverse sample of 164 chromosomes). We discuss the implications of using cohorts of different size and ethnic composition and the usefulness of public SNP databases for this effort. Finally, we estimate the experimental effort and cost required to complete a genome-wide haplotype survey.

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Year:  2002        PMID: 12052145     DOI: 10.1517/14622416.3.3.379

Source DB:  PubMed          Journal:  Pharmacogenomics        ISSN: 1462-2416            Impact factor:   2.533


  18 in total

1.  High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools.

Authors:  Karen L Mohlke; Michael R Erdos; Laura J Scott; Tasha E Fingerlin; Anne U Jackson; Kaisa Silander; Pablo Hollstein; Michael Boehnke; Francis S Collins
Journal:  Proc Natl Acad Sci U S A       Date:  2002-12-13       Impact factor: 11.205

2.  Recovering frequencies of known haplotype blocks from single-nucleotide polymorphism allele frequencies.

Authors:  Itsik Pe'er; Jacques S Beckmann
Journal:  Genetics       Date:  2004-04       Impact factor: 4.562

3.  Finding haplotype tagging SNPs by use of principal components analysis.

Authors:  Zhen Lin; Russ B Altman
Journal:  Am J Hum Genet       Date:  2004-09-23       Impact factor: 11.025

4.  Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes.

Authors:  Roberto Romero; Digna R Velez Edwards; Juan Pedro Kusanovic; Sonia S Hassan; Shali Mazaki-Tovi; Edi Vaisbuch; Chong Jai Kim; Tinnakorn Chaiworapongsa; Brad D Pearce; Lara A Friel; Jacquelaine Bartlett; Madan Kumar Anant; Benjamin A Salisbury; Gerald F Vovis; Min Seob Lee; Ricardo Gomez; Ernesto Behnke; Enrique Oyarzun; Gerard Tromp; Scott M Williams; Ramkumar Menon
Journal:  Am J Obstet Gynecol       Date:  2010-05       Impact factor: 8.661

5.  Strong correlation between meiotic crossovers and haplotype structure in a 2.5-Mb region on the long arm of chromosome 21.

Authors:  Danielle M Greenawalt; Xiangfeng Cui; Yujun Wu; Yong Lin; Hui-Yun Wang; Minjie Luo; Irina V Tereshchenko; Guohong Hu; James Y Li; Yi Chu; Marco A Azaro; Christina J Decoste; Nyam-Osor Chimge; Richeng Gao; Li Shen; Weichung J Shih; Kenneth Lange; Honghua Li
Journal:  Genome Res       Date:  2005-12-29       Impact factor: 9.043

Review 6.  Recent developments in genomewide association scans: a workshop summary and review.

Authors:  Duncan C Thomas; Robert W Haile; David Duggan
Journal:  Am J Hum Genet       Date:  2005-08-01       Impact factor: 11.025

7.  A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM).

Authors:  Roberto Romero; Lara A Friel; Digna R Velez Edwards; Juan Pedro Kusanovic; Sonia S Hassan; Shali Mazaki-Tovi; Edi Vaisbuch; Chong Jai Kim; Offer Erez; Tinnakorn Chaiworapongsa; Brad D Pearce; Jacquelaine Bartlett; Benjamin A Salisbury; Madan Kumar Anant; Gerald F Vovis; Min Seob Lee; Ricardo Gomez; Ernesto Behnke; Enrique Oyarzun; Gerard Tromp; Scott M Williams; Ramkumar Menon
Journal:  Am J Obstet Gynecol       Date:  2010-07-31       Impact factor: 8.661

8.  Polymorphisms in maternal and fetal genes encoding for proteins involved in extracellular matrix metabolism alter the risk for small-for-gestational-age.

Authors:  Digna R Velez Edwards; Roberto Romero; Juan Pedro Kusanovic; Sonia S Hassan; Shali Mazaki-Tovi; Edi Vaisbuch; Chong Jai Kim; Offer Erez; Tinnakorn Chaiworapongsa; Brad D Pearce; Jacquelaine Bartlett; Lara A Friel; Benjamin A Salisbury; Madan Kumar Anant; Gerald F Vovis; Min Seob Lee; Ricardo Gomez; Ernesto Behnke; Enrique Oyarzun; Gerard Tromp; Ramkumar Menon; Scott M Williams
Journal:  J Matern Fetal Neonatal Med       Date:  2010-07-09

9.  Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genome.

Authors:  Andrew G Clark; Rasmus Nielsen; James Signorovitch; Tara C Matise; Stephen Glanowski; Jeremy Heil; Emily S Winn-Deen; Arthur L Holden; Eric Lai
Journal:  Am J Hum Genet       Date:  2003-07-03       Impact factor: 11.025

10.  Conceptualizing race in research.

Authors:  Giselle Corbie-Smith; Gail Henderson; Connie Blumenthal; Jessica Dorrance; Sue Estroff
Journal:  J Natl Med Assoc       Date:  2008-10       Impact factor: 1.798

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