Literature DB >> 12960966

Large-scale genotyping of complex DNA.

Giulia C Kennedy1, Hajime Matsuzaki, Shoulian Dong, Wei-min Liu, Jing Huang, Guoying Liu, Xing Su, Manqiu Cao, Wenwei Chen, Jane Zhang, Weiwei Liu, Geoffrey Yang, Xiaojun Di, Thomas Ryder, Zhijun He, Urvashi Surti, Michael S Phillips, Michael T Boyce-Jacino, Stephen P A Fodor, Keith W Jones.   

Abstract

Genetic studies aimed at understanding the molecular basis of complex human phenotypes require the genotyping of many thousands of single-nucleotide polymorphisms (SNPs) across large numbers of individuals. Public efforts have so far identified over two million common human SNPs; however, the scoring of these SNPs is labor-intensive and requires a substantial amount of automation. Here we describe a simple but effective approach, termed whole-genome sampling analysis (WGSA), for genotyping thousands of SNPs simultaneously in a complex DNA sample without locus-specific primers or automation. Our method amplifies highly reproducible fractions of the genome across multiple DNA samples and calls genotypes at >99% accuracy. We rapidly genotyped 14,548 SNPs in three different human populations and identified a subset of them with significant allele frequency differences between groups. We also determined the ancestral allele for 8,386 SNPs by genotyping chimpanzee and gorilla DNA. WGSA is highly scaleable and enables the creation of ultrahigh density SNP maps for use in genetic studies.

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Year:  2003        PMID: 12960966     DOI: 10.1038/nbt869

Source DB:  PubMed          Journal:  Nat Biotechnol        ISSN: 1087-0156            Impact factor:   54.908


  177 in total

1.  Selective DNA amplification from complex genomes using universal double-sided adapters.

Authors:  Matthew J Callow; Snezana Drmanac; Radoje Drmanac
Journal:  Nucleic Acids Res       Date:  2004-01-28       Impact factor: 16.971

2.  High-resolution analysis of DNA copy number using oligonucleotide microarrays.

Authors:  Graham R Bignell; Jing Huang; Joel Greshock; Stephen Watt; Adam Butler; Sofie West; Mira Grigorova; Keith W Jones; Wen Wei; Michael R Stratton; P Andrew Futreal; Barbara Weber; Michael H Shapero; Richard Wooster
Journal:  Genome Res       Date:  2004-02       Impact factor: 9.043

3.  Genome coverage and sequence fidelity of phi29 polymerase-based multiple strand displacement whole genome amplification.

Authors:  J Guillermo Paez; Ming Lin; Rameen Beroukhim; Jeffrey C Lee; Xiaojun Zhao; Daniel J Richter; Stacey Gabriel; Paula Herman; Hidefumi Sasaki; David Altshuler; Cheng Li; Matthew Meyerson; William R Sellers
Journal:  Nucleic Acids Res       Date:  2004-05-18       Impact factor: 16.971

4.  Allelic imbalance analysis by high-density single-nucleotide polymorphic allele (SNP) array with whole genome amplified DNA.

Authors:  Kwong-Kwok Wong; Yvonne T M Tsang; Jianhe Shen; Rita S Cheng; Yi-Mieng Chang; Tsz-Kwong Man; Ching C Lau
Journal:  Nucleic Acids Res       Date:  2004-05-17       Impact factor: 16.971

5.  Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps.

Authors:  David M Evans; Lon R Cardon
Journal:  Am J Hum Genet       Date:  2004-08-13       Impact factor: 11.025

6.  Sequence-based linkage analysis.

Authors:  Itay Furman; Mark J Rieder; Suzanne Da Ponte; Dana P Carrington; Deborah A Nickerson; Leonid Kruglyak; Kyriacos Markianos
Journal:  Am J Hum Genet       Date:  2004-08-25       Impact factor: 11.025

7.  Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.

Authors:  F A Middleton; M T Pato; K L Gentile; C P Morley; X Zhao; A F Eisener; A Brown; T L Petryshen; A N Kirby; H Medeiros; C Carvalho; A Macedo; A Dourado; I Coelho; J Valente; M J Soares; C P Ferreira; M Lei; M H Azevedo; J L Kennedy; M J Daly; P Sklar; C N Pato
Journal:  Am J Hum Genet       Date:  2004-04-01       Impact factor: 11.025

8.  Decoding randomly ordered DNA arrays.

Authors:  Kevin L Gunderson; Semyon Kruglyak; Michael S Graige; Francisco Garcia; Bahram G Kermani; Chanfeng Zhao; Diping Che; Todd Dickinson; Eliza Wickham; Jim Bierle; Dennis Doucet; Monika Milewski; Robert Yang; Chris Siegmund; Juergen Haas; Lixin Zhou; Arnold Oliphant; Jian-Bing Fan; Steven Barnard; Mark S Chee
Journal:  Genome Res       Date:  2004-04-12       Impact factor: 9.043

9.  Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array.

Authors:  Hajime Matsuzaki; Halina Loi; Shoulian Dong; Ya-Yu Tsai; Joy Fang; Jane Law; Xiaojun Di; Wei-Min Liu; Geoffrey Yang; Guoying Liu; Jing Huang; Giulia C Kennedy; Thomas B Ryder; Gregory A Marcus; P Sean Walsh; Mark D Shriver; Jennifer M Puck; Keith W Jones; Rui Mei
Journal:  Genome Res       Date:  2004-03       Impact factor: 9.043

10.  RYR1 mutations as a cause of ophthalmoplegia, facial weakness, and malignant hyperthermia.

Authors:  Sherin Shaaban; Leigh Ramos-Platt; Floyd H Gilles; Wai-Man Chan; Caroline Andrews; Umberto De Girolami; Joseph Demer; Elizabeth C Engle
Journal:  JAMA Ophthalmol       Date:  2013-12       Impact factor: 7.389

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