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Nøkkelord: 0-useful [18 articles]

Nye artikler klassifisert med nøkkelordet 0-useful.
  • The chicken genome: some good news and some bad news.
    Poult Sci, Vol. 86, No. 7. (July 2007), pp. 1453-1459.
    by JB Dodgson
    posted to chicken 0-useful by sleepingcell to the group Bioinformatics on 2007-06-19 16:08:50 as read
  • High-throughput genotyping of intermediate-size structural variation
    Human Molecular Genetics, Vol. 15, No. 7. (1 April 2006), pp. 1159-1167.
    by Tera L Newman, Mark J Rieder, Anne V Morrison, Andrew J Sharp, Joshua D Smith, James L Sprague, Rajinder Kaul, Christopher S Carlson, Maynard V Olson, Deborah A Nickerson, Evan E Eichler
    posted to variation 0-useful by sleepingcell to the group Bioinformatics on 2007-07-19 10:43:48 as read
  • MicroRNA function in animal development
    FEBS Letters, Vol. 579, No. 26. (31 October 2005), pp. 5911-5922.
    by Erno Wienholds, Ronald H Plasterk
    posted to mirna 0-useful by sleepingcell to the group Bioinformatics on 2007-06-11 10:21:11 as **
  • Polymorphic miRNA-mediated gene regulation: contribution to phenotypic variation and disease.
    Curr Opin Genet Dev (27 April 2007)
    by Michel Georges, Wouter Coppieters, Carole Charlier
  • Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data.
    Bioinformatics (4 August 2005)
    by Weil R R Lai, Mark D D Johnson, Raju Kucherlapati, Peter J J Park
  • Comparative genomic hybridization.
    Annu Rev Genomics Hum Genet, Vol. 6 (2005), pp. 331-354.
    by D Pinkel, DG Albertson
    posted to cnv 0-useful by sleepingcell to the group Bioinformatics on 2007-04-19 19:14:44 as read along with 1 person uz_labu_laimi
  • Natural genetic variation caused by transposable elements in humans.
    Genetics, Vol. 168, No. 2. (October 2004), pp. 933-951.
    by EA Bennett, LE Coleman, C Tsui, WS Pittard, SE Devine
    posted to variation 0-useful by sleepingcell to the group Bioinformatics on 2007-06-27 16:41:50 as read along with 2 people bpb yoanjacquemin
  • Genome-wide Copy Number Profiling on High-density Bacterial Artificial Chromosomes, Single-nucleotide Polymorphisms, and Oligonucleotide Microarrays: A Platform Comparison based on Statistical Power Analysis.
    DNA Res (15 March 2007)
    by Jayne Y Y Hehir-Kwa, Michael Egmont-Petersen, Irene M M Janssen, Dominique Smeets, Ad Geurts G van Kessel, Joris A A Veltman
    posted to cnv 0-useful by sleepingcell to the group Bioinformatics on 2007-04-19 18:19:26 as *** along with 1 person jfr
  • A comparison study: applying segmentation to array CGH data for downstream analyses.
    Bioinformatics (14 September 2005)
    by Hanni Willenbrock, Jane Fridlyand
    posted to cnv 0-useful by sleepingcell to the group Bioinformatics on 2007-04-20 08:24:09 as read along with 4 people pcahan1 archroad rdiaz OscarRueda
  • Array comparative genomic hybridization and its applications in cancer.
    Nat Genet, Vol. 37 Suppl (June 2005)
    by D Pinkel, DG Albertson
  • A mutation creating a potential illegitimate microRNA target site in the myostatin gene affects muscularity in sheep
    Nature Genetics, Vol. 38, No. 7. (04 June 2006), pp. 813-818.
    by Alex Clop, Fabienne Marcq, Haruko Takeda, Dimitri Pirottin, Xavier Tordoir, Bernard Bibé, Jacques Bouix, Florian Caiment, Jean-Michel Elsen, Francis Eychenne, Catherine Larzul, Elisabeth Laville, Françoise Meish, Dragan Milenkovic, James Tobin, Carole Charlier, Michel Georges
  • Human polymorphism at microRNAs and microRNA target sites.
    Proc Natl Acad Sci U S A, Vol. 104, No. 9. (27 February 2007), pp. 3300-3305.
    by MA Saunders, H Liang, WH Li
  • 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 versatile statistical analysis algorithm to detect genome copy number variation.
    Proc Natl Acad Sci U S A, Vol. 101, No. 46. (16 November 2004), pp. 16292-16297.
    by RS Daruwala, A Rudra, H Ostrer, R Lucito, M Wigler, B Mishra
    posted to cnv 0-useful by sleepingcell to the group Bioinformatics on 2007-04-19 19:16:04 as read along with 3 people rdiaz OscarRueda bioguru2000
  • Completing the map of human genetic variation
    Nature, Vol. 447, No. 7141. (10 May 2007), pp. 161-165.
  • Natural selection on human microRNA binding sites inferred from SNP data.
    Nat Genet (29 October 2006)
    by Kevin Chen, Nikolaus Rajewsky
  • A genetic variation map for chicken with 2.8 million single-nucleotide polymorphisms.
    Nature, Vol. 432, No. 7018. (9 December 2004), pp. 717-722.
    by GK Wong, B Liu, J Wang, Y Zhang, X Yang, Z Zhang, Q Meng, J Zhou, D Li, J Zhang, P Ni, S Li, L Ran, H Li, J Zhang, R Li, S Li, H Zheng, W Lin, G Li, X Wang, W Zhao, J Li, C Ye, M Dai, J Ruan, Y Zhou, Y Li, X He, Y Zhang, J Wang, X Huang, W Tong, J Chen, J Ye, C Chen, N Wei, G Li, L Dong, F Lan, Y Sun, Z Zhang, Z Yang, Y Yu, Y Huang, D He, Y Xi, D Wei, Q Qi, W Li, J Shi, M Wang, F Xie, J Wang, X Zhang, P Wang, Y Zhao, N Li, N Yang, W Dong, S Hu, C Zeng, W Zheng, B Hao, LW Hillier, SP Yang, WC Warren, RK Wilson, M Brandström, H Ellegren, RP Crooijmans, JJ van der Poel, H Bovenhuis, MA Groenen, I Ovcharenko, L Gordon, L Stubbs, S Lucas, T Glavina, A Aerts, P Kaiser, L Rothwell, JR Young, S Rogers, BA Walker, A van Hateren, J Kaufman, N Bumstead, SJ Lamont, H Zhou, PM Hocking, D Morrice, DJ de Koning, A Law, N Bartley, DW Burt, H Hunt, HH Cheng, U Gunnarsson, P Wahlberg, L Andersson, E Kindlund, MT Tammi, B Andersson, C Webber, CP Ponting, IM Overton, PE Boardman, H Tang, SJ Hubbard, SA Wilson, J Yu, J Wang, H Yang,
    posted to snp chicken 0-useful by sleepingcell to the group Bioinformatics on 2007-04-03 05:27:27 as read
  • The genomic landscape of short insertion and deletion polymorphisms in the chicken (Gallus gallus) genome: a high frequency of deletions in tandem duplicates.
    Genetics (16 May 2007)
    by Mikael Brandstrom, Hans Ellegren
    posted to variation snp chicken 0-useful by sleepingcell to the group Bioinformatics on 2007-05-18 15:17:17 as read
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