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waszak's snp [10 articles]

当前文献位于 waszak's 文献库 标签分类为 snp. You can also see everyone's snp.
  • Integrated detection and population-genetic analysis of SNPs and copy number variation.
    Nature genetics (7 September 2008)
    by Steven A A McCarroll, Finny G G Kuruvilla, Joshua M M Korn, Simon Cawley, James Nemesh, Alec Wysoker, Michael H H Shapero, Paul I W I de Bakker, Julian B B Maller, Andrew Kirby, Amanda L L Elliott, Melissa Parkin, Earl Hubbell, Teresa Webster, Rui Mei, James Veitch, Patrick J J Collins, Robert Handsaker, Steve Lincoln, Marcia Nizzari, John Blume, Keith W W Jones, Rich Rava, Mark J J Daly, Stacey B B Gabriel, David Altshuler
  • A robust statistical method for case-control association testing with copy number variation.
    Nature genetics (7 September 2008)
    by Chris Barnes, Vincent Plagnol, Tomas Fitzgerald, Richard Redon, Jonathan Marchini, David Clayton, Matthew E E Hurles
  • QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.
    Nucleic Acids Res (27 March 2007)
    by Stefano Colella, Christopher Yau, Jennifer M M Taylor, Ghazala Mirza, Helen Butler, Penny Clouston, Anne S S Bassett, Anneke Seller, Christopher C C Holmes, Jiannis Ragoussis
  • Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays
    Genome Res., Vol. 16, No. 12. (1 December 2006), pp. 1575-1584.
    by Daisuke Komura, Fan Shen, Shumpei Ishikawa, Karen R Fitch, Wenwei Chen, Jane Zhang, Guoying Liu, Sigeo Ihara, Hiroshi Nakamura, Matthew E Hurles, Charles Lee, Stephen W Scherer, Keith W Jones, Michael H Shapero, Jing Huang, Hiroyuki Aburatani
  • A high-resolution survey of deletion polymorphism in the human genome
    Nature Genetics, Vol. 38, No. 1. (04 December 2005), pp. 75-81.
    by Donald F Conrad, Daniel T Andrews, Nigel P Carter, Matthew E Hurles, Jonathan K Pritchard
  • Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.
    Am J Hum Genet, Vol. 79, No. 2. (August 2006), pp. 275-290.
    by DP Locke, AJ Sharp, SA McCarroll, SD McGrath, TL Newman, Z Cheng, S Schwartz, DG Albertson, D Pinkel, DM Altshuler, EE Eichler
    posted to snp ld human hapmap genome cnv cnp by waszak on 2008-10-08 14:36:13 as ** along with 1 person lp2
  • Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies
    PLoS Genetics, Vol. 3, No. 10. (1 October 2007), e190.
    by Xavier Estivill, Lluís Armengol
    posted to snp gwas genome cnv by waszak on 2008-10-08 14:32:56 as ** along with 2 people jfr giovanni
  • Systematic assessment of copy number variant detection via genome-wide SNP genotyping.
    Nature genetics (7 September 2008)
    by Gregory M M Cooper, Troy Zerr, Jeffrey M M Kidd, Evan E E Eichler, Deborah A A Nickerson
  • Effect of polymorphisms within probe-target sequences on olignonucleotide microarray experiments
    Nucl. Acids Res., Vol. 36, No. 13. (1 August 2008), pp. 4417-4423.
    by David Benovoy, Tony Kwan, Jacek Majewski
  • Copy Number Variation Detection via High-Density SNP Genotyping
    Cold Spring Harbor Protocols, Vol. 2008, No. 7. (1 June 2008), pdb.top46.
    by Kai Wang, Maja Bucan
    posted to cnv genotyping snp by waszak on 2008-07-19 22:21:28 as **
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