Literature DB >> 15961272

High-density single-nucleotide polymorphism maps of the human genome.

Raymond D Miller1, Michael S Phillips, Inho Jo, Miriam A Donaldson, Joel F Studebaker, Nicholas Addleman, Steven V Alfisi, Wendy M Ankener, Hamid A Bhatti, Chad E Callahan, Benjamin J Carey, Cheryl L Conley, Justin M Cyr, Vram Derohannessian, Rachel A Donaldson, Carolina Elosua, Stacey E Ford, Angela M Forman, Craig A Gelfand, Nicole M Grecco, Susan M Gutendorf, Cricket R Hock, Mark J Hozza, Soyoung Hur, Sun Mi In, Diana L Jackson, Sangmee Ahn Jo, Sung-Chul Jung, Sook Kim, Kuchan Kimm, Ellen F Kloss, Daniel C Koboldt, Jennifer M Kuebler, Feng-Shen Kuo, Jessica A Lathrop, Jong-Keuk Lee, Kathy L Leis, Stephanie A Livingston, Elizabeth G Lovins, Maria L Lundy, Sima Maggan, Matthew Minton, Michael A Mockler, David W Morris, Eric P Nachtman, Bermseok Oh, Chan Park, Chang-Wook Park, Nicholas Pavelka, Adrienne B Perkins, Stephanie L Restine, Ravi Sachidanandam, Andrew J Reinhart, Kathryn E Scott, Gira J Shah, Jatana M Tate, Shobha A Varde, Amy Walters, J Rebecca White, Yeon-Kyeong Yoo, Jong-Eun Lee, Michael T Boyce-Jacino, Pui-Yan Kwok.   

Abstract

Here we report a large, extensively characterized set of single-nucleotide polymorphisms (SNPs) covering the human genome. We determined the allele frequencies of 55,018 SNPs in African Americans, Asians (Japanese-Chinese), and European Americans as part of The SNP Consortium's Allele Frequency Project. A subset of 8333 SNPs was also characterized in Koreans. Because these SNPs were ascertained in the same way, the data set is particularly useful for modeling. Our results document that much genetic variation is shared among populations. For autosomes, some 44% of these SNPs have a minor allele frequency > or =10% in each population, and the average allele frequency differences between populations with different continental origins are less than 19%. However, the several percentage point allele frequency differences among the closely related Korean, Japanese, and Chinese populations suggest caution in using mixtures of well-established populations for case-control genetic studies of complex traits. We estimate that approximately 7% of these SNPs are private SNPs with minor allele frequencies <1%. A useful set of characterized SNPs with large allele frequency differences between populations (>60%) can be used for admixture studies. High-density maps of high-quality, characterized SNPs produced by this project are freely available.

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Year:  2005        PMID: 15961272      PMCID: PMC1885222          DOI: 10.1016/j.ygeno.2005.04.012

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  33 in total

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Authors:  L Picoult-Newberg; T E Ideker; M G Pohl; S L Taylor; M A Donaldson; D A Nickerson; M Boyce-Jacino
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4.  Primer design and marker clustering for multiplex SNP-IT primer extension genotyping assay using statistical modeling.

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10.  Comparative analysis of human DNA variations by fluorescence-based sequencing of PCR products.

Authors:  P Y Kwok; C Carlson; T D Yager; W Ankener; D A Nickerson
Journal:  Genomics       Date:  1994-09-01       Impact factor: 5.736

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2.  Mapping genes that predict treatment outcome in admixed populations.

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Review 9.  NCI, NHLBI first international consensus conference on late effects after pediatric hematopoietic cell transplantation: etiology and pathogenesis of late effects after HCT performed in childhood--methodologic challenges.

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10.  Targeted resequencing and analysis of the Diamond-Blackfan anemia disease locus RPS19.

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