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di jyuh cnv [19 articles]

Articoli aggiunti di recente alla biblioteca di jyuh classificati sotto il tag cnv. You can also see everyone's cnv.
  • Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.
    Nature genetics (7 September 2008)
    by Joshua M M Korn, Finny G G Kuruvilla, Steven A A McCarroll, Alec Wysoker, James Nemesh, Simon Cawley, Earl Hubbell, Jim Veitch, Patrick J J Collins, Katayoon Darvishi, Charles Lee, Marcia M M Nizzari, Stacey B B Gabriel, Shaun Purcell, Mark J J Daly, David Altshuler
  • Genetic variation in human disease and a new role for copy number variants.
    Mutation research, Vol. 622, No. 1-2. (1 September 2007), pp. 33-41.
    by AN Shelling, LR Ferguson
    posted to snp cnv by jyuh on 2008-10-04 03:45:02 as **
  • 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
  • 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
  • A novel technique for measuring variations in DNA copy-number: competitive genomic polymerase chain reaction
    BMC Genomics, Vol. 8 (02 July 2007), 206.
    by Kyoko Iwao-Koizumi, Kazunori Maekawa, Yohko Nakamura, Sakae Saito, Shoko Kawamoto, Akira Nakagawara, Kikuya Kato
    posted to cnv pcr by jyuh on 2008-08-27 02:48:18 as **
  • Impact of whole genome amplification on analysis of copy number variants.
    Nucleic acids research, Vol. 36, No. 13. (August 2008)
    by TJ Pugh, AD Delaney, N Farnoud, S Flibotte, M Griffith, HI Li, H Qian, P Farinha, RD Gascoyne, MA Marra
    posted to cnv wga by jyuh on 2008-08-10 07:24:23 as ** along with 2 people and 1 group stajich nuin Berkeley Mycology
  • MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data.
    Bioinformatics (Oxford, England), Vol. 24, No. 14. (15 July 2008), pp. 1645-1646.
    by M Kato, Y Nakamura, T Tsunoda
    posted to cnv haplotype software by jyuh on 2008-07-25 08:36:38 as **
  • Hidden copy number variation in the HapMap population.
    Proceedings of the National Academy of Sciences of the United States of America, Vol. 105, No. 29. (22 July 2008), pp. 10067-10072.
    by JC Marioni, M White, S Tavaré, AG Lynch
  • An Algorithm for Inferring Complex Haplotypes in a Region of Copy-Number Variation.
    American journal of human genetics (16 July 2008)
    by Mamoru Kato, Yusuke Nakamura, Tatsuhiko Tsunoda
    posted to cnv haplotype by jyuh on 2008-07-25 06:53:12 as **
  • Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.
    Human mutation (9 May 2008)
    by Chien-Hsing H Lin, Mei-Chu C Huang, Ling-Hui H Li, Jer-Yuarn Y Wu, Yuan-Tsong T Chen, Cathy S J S Fann
    posted to cnv pooling by jyuh on 2008-07-25 06:52:47 as **
  • Genotype, haplotype and copy-number variation in worldwide human populations
    Nature, Vol. 451, No. 7181. (21 February 2008), pp. 998-1003.
    by Mattias Jakobsson, Sonja W Scholz, Paul Scheet, Raphael J Gibbs, Jenna M Vanliere, Hon-Chung Fung, Zachary A Szpiech, James H Degnan, Kai Wang, Rita Guerreiro, Jose M Bras, Jennifer C Schymick, Dena G Hernandez, Bryan J Traynor, Javier Simon-Sanchez, Mar Matarin, Angela Britton, Joyce van de Leemput, Ian Rafferty, Maja Bucan, Howard M Cann, John A Hardy, Noah A Rosenberg, Andrew B Singleton
  • Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes
    BMC Genetics, Vol. 9 (28 March 2008), 27.
    by Fan Shen, Jing Huang, Karen R Fitch, Vivi B Truong, Andrew Kirby, Wenwei Chen, Jane Zhang, Guoying Liu, Steven A Mccarroll, Keith W Jones, Michael H Shapero
    posted to microarray cnv by jyuh on 2008-07-25 06:35:06 as ** along with 1 person daed
  • The Fine-Scale and Complex Architecture of Human Copy-Number Variation.
    Am J Hum Genet (24 January 2008)
    by George H H Perry, Amir Ben-Dor, Anya Tsalenko, Nick Sampas, Laia Rodriguez-Revenga, Charles W W Tran, Alicia Scheffer, Israel Steinfeld, Peter Tsang, N Alice A Yamada, Han Soo S Park, Jong-Il I Kim, Jeong-Sun S Seo, Zohar Yakhini, Stephen Laderman, Laurakay Bruhn, Charles Lee
    posted to cnv by jyuh on 2008-07-25 06:34:56 as ** along with 2 people vplagnol daed
  • What a difference copy number variation makes
    BioEssays, Vol. 29, No. 4. (2007), pp. 311-313.
    by Hildegard Kehrer-Sawatzki
  • On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test.
    Genetic epidemiology, Vol. 32, No. 3. (April 2008), pp. 273-284.
    by I Ionita-Laza, GH Perry, BA Raby, B Klanderman, C Lee, NM Laird, ST Weiss, C Lange
    posted to cnv family gwa software by jyuh on 2008-07-25 06:28:17 as ** along with 1 person vplagnol
  • MD-SeeGH: a platform for integrative analysis of multi-dimensional genomic data
    BMC Bioinformatics, Vol. 9 (20 May 2008), 243.
    by Bryan Chi, Ronald J Deleeuw, Bradley P Coe, Raymond T Ng, Calum Macaulay, Wan L Lam
    posted to software snp microarray cnv cgh by jyuh on 2008-07-14 03:59:13 as ** along with 1 person jfr
  • SNPExpress: integrated visualization of genome-wide genotypes, copy numbers and gene expression levels.
    BMC Genomics, Vol. 9, No. 1. (25 January 2008)
    by Mathijs A Sanders, Roel G Verhaak, Wendy M Geertsma-Kleinekoort, Saman Abbas, Sebastiaan Horsman, Peter J van der Spek, Bob Lowenberg, Peter J Valk
    posted to software snp microarray gwa cnv by jyuh on 2008-02-01 15:00:08 as ** along with 1 person jfr
  • Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes
    Science, Vol. 315, No. 5813. (9 February 2007), pp. 848-853.
    by Barbara E Stranger, Matthew S Forrest, Mark Dunning, Catherine E Ingle, Claude Beazley, Natalie Thorne, Richard Redon, Christine P Bird, Anna de Grassi, Charles Lee, Chris Tyler-Smith, Nigel Carter, Stephen W Scherer, Simon Tavare, Panagiotis Deloukas, Matthew E Hurles, Emmanouil T Dermitzakis
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