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jfrs cnv [7 articles]

Senaste hänvisningarna i jfrs bibliotek insorterade under taggen cnv. You can also see everyone's cnv.
  • wuHMM: a robust algorithm to detect DNA copy number variation using long oligonucleotide microarray data.
    Nucleic acids research, Vol. 36, No. 7. (April 2008)
    by P Cahan, LE Godfrey, PS Eis, TA Richmond, RR Selzer, M Brent, HL McLeod, TJ Ley, TA Graubert
    posted to array-cgh cnv copy-number methodology by jfr on 2008-06-27 17:08:57 as **
  • A genome-wide approach to identify genetic variants that contribute to etoposide-induced cytotoxicity.
    Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, No. 23. (5 June 2007), pp. 9758-9763.
    by RS Huang, S Duan, WK Bleibel, EO Kistner, W Zhang, TA Clark, TX Chen, AC Schweitzer, JE Blume, NJ Cox, ME Dolan
    posted to cnv exon_arrays snp-arrays treatment by jfr on 2008-06-11 09:23:54 as **
  • Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization
    Genome Biology, Vol. 8 (25 October 2007), R228.
    by John C Marioni, Natalie P Thorne, Armand Valsesia, Tomas Fitzgerald, Richard Redon, Heike Fiegler, Daniel T Andrews, Barbara E Stranger, Andrew G Lynch, Emmanouil T Dermitzakis, Nigel P Carter, Simon Tavare, Matthew E Hurles
    posted to cnv methodology software by jfr on 2008-03-17 16:12:56 as ** along with 2 people jlangdon sanchezbuelna
  • Assessing the Significance of Conserved Genomic Aberrations Using High Resolution Genomic Microarrays
    PLoS Genetics, Vol. 3, No. 8. (1 August 2007), e143.
    by Mitchell Guttman, Carolyn Mies, Katarzyna Dudycz-Sulicz, Sharon J Diskin, Don A Baldwin, Christian J Stoeckert, Gregory R Grant
    posted to cnv copy-number methodology software by jfr on 2008-02-29 11:11:50 as read along with 3 people and 2 groups rdiaz ealloza zwang Bioinformatics BioinfoCIPF
  • Toward accurate high-throughput SNP genotyping in the presence of inherited copy number variation
    BMC Genomics, Vol. 8 (03 July 2007), 211.
    by Laura E Macconaill, Micheala A Aldred, Xincheng Lu, Thomas Laframboise
    posted to cnv genotyping snp-arrays by jfr on 2008-02-13 13:49:23 as **
  • Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome.
    Science (27 September 2007)
    by Jan O O Korbel, Alexander Eckehart E Urban, Jason P P Affourtit, Brian Godwin, Fabian Grubert, Jan Fredrik F Simons, Philip M M Kim, Dean Palejev, Nicholas J J Carriero, Lei Du, Bruce E E Taillon, Zhoutao Chen, Andrea Tanzer, A C Eugenia C Saunders, Jianxiang Chi, Fengtang Yang, Nigel P P Carter, Matthew E E Hurles, Sherman M M Weissman, Timothy T T Harkins, Mark B B Gerstein, Michael Egholm, Michael Snyder
    posted to cnv copy-number genomics by jfr on 2007-12-17 12:01:03 as read along with 9 people and 1 group dpollard dchughes AaronDarling rdiaz giovanni jlangdon annacarina07 Neeperando caseybrown EisenLab
  • 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
    posted to cnv copy-number hapmap snp by jfr on 2007-05-29 17:13:17 as ** along with 15 people and 3 groups srp33 jyuh dpollard balicea rdiaz qfwills djkt vplagnol shigepong jlangdon xingxu cisevol caseybrown frohike jandot Bioinformatics EisenLab cis-regulatory-evolution
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