Literature DB >> 17225249

Whole genome genotyping technologies on the BeadArray platform.

Frank J Steemers1, Kevin L Gunderson.   

Abstract

The ability to simultaneously genotype hundreds of thousands of single-nucleotide polymorphisms (SNPs) in a single assay has recently become feasible due to innovative combinations of assay and array platform multiplexing. In this review, we describe the development of the Infinium whole genome genotyping technology and the BeadArray platform. We discuss the automated use and performance of a series of genotyping BeadChips, including data quality, technology scalability, and flexibility in designing array content. We describe high-density tag SNP-based Bead-Chips and various multi-sample BeadChip configurations with their respective applications. These technologies are enabling large-scale whole genome association studies that have the potential to revolutionize our ability to detect common genetic variants with a significant role in identifying disease-associated loci, proteins, biomarkers, and pharmacogenomic responses.

Mesh:

Year:  2007        PMID: 17225249     DOI: 10.1002/biot.200600213

Source DB:  PubMed          Journal:  Biotechnol J        ISSN: 1860-6768            Impact factor:   4.677


  81 in total

1.  Enhancing radiation hybrid mapping through whole genome amplification.

Authors:  Genesio M Karere; Leslie A Lyons; Lutz Froenicke
Journal:  Hereditas       Date:  2010-04       Impact factor: 3.271

2.  Insights into colon cancer etiology via a regularized approach to gene set analysis of GWAS data.

Authors:  Lin S Chen; Carolyn M Hutter; John D Potter; Yan Liu; Ross L Prentice; Ulrike Peters; Li Hsu
Journal:  Am J Hum Genet       Date:  2010-06-11       Impact factor: 11.025

3.  Chediak-Higashi syndrome with early developmental delay resulting from paternal heterodisomy of chromosome 1.

Authors:  Irini Manoli; Gretchen Golas; Wendy Westbroek; Thierry Vilboux; Thomas C Markello; Wendy Introne; Dawn Maynard; Ben Pederson; Ekaterini Tsilou; Michael B Jordan; P Suzanne Hart; James G White; William A Gahl; Marjan Huizing
Journal:  Am J Med Genet A       Date:  2010-06       Impact factor: 2.802

4.  Magnetic assembly of high-density DNA arrays for genomic analyses.

Authors:  Kristopher D Barbee; Xiaohua Huang
Journal:  Anal Chem       Date:  2008-02-09       Impact factor: 6.986

Review 5.  New technologies for delineating and characterizing the lipid exome: prospects for understanding familial combined hyperlipidemia.

Authors:  Stuart D Horswell; Helen E Ringham; Carol C Shoulders
Journal:  J Lipid Res       Date:  2008-11-20       Impact factor: 5.922

Review 6.  Integrative systems biology for data-driven knowledge discovery.

Authors:  Casey S Greene; Olga G Troyanskaya
Journal:  Semin Nephrol       Date:  2010-09       Impact factor: 5.299

7.  PRKCA: a positional candidate gene for body mass index and asthma.

Authors:  Amy Murphy; Kelan G Tantisira; Manuel E Soto-Quirós; Lydiana Avila; Barbara J Klanderman; Stephen Lake; Scott T Weiss; Juan C Celedón
Journal:  Am J Hum Genet       Date:  2009-07-02       Impact factor: 11.025

8.  Kernel-based association test.

Authors:  Hsin-Chou Yang; Hsin-Yi Hsieh; Cathy S J Fann
Journal:  Genetics       Date:  2008-06       Impact factor: 4.562

Review 9.  A HapMap harvest of insights into the genetics of common disease.

Authors:  Teri A Manolio; Lisa D Brooks; Francis S Collins
Journal:  J Clin Invest       Date:  2008-05       Impact factor: 14.808

10.  20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits.

Authors:  S R Lalani; J V Thakuria; G F Cox; X Wang; W Bi; M S Bray; C Shaw; S W Cheung; A C Chinault; B A Boggs; Z Ou; E K Brundage; J R Lupski; J Gentile; S Waisbren; A Pursley; L Ma; M Khajavi; G Zapata; R Friedman; J J Kim; J A Towbin; P Stankiewicz; S Schnittger; I Hansmann; T Ai; S Sood; X H Wehrens; J F Martin; J W Belmont; L Potocki
Journal:  J Med Genet       Date:  2008-09-23       Impact factor: 6.318

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