Регистрация | Вход в службу | FAQ      [?] 

Ключевое слово nssnps [29 articles]

Recent papers classified by the tag nssnps.
  • TAMAL: an integrated approach to choosing SNPs for genetic studies of human complex traits
    Bioinformatics, Vol. 22, No. 5. (1 March 2006), pp. 626-627.
    by Bradley M Hemminger, Billy Saelim, Patrick F Sullivan
    posted to nssnps by ramensky on 2007-02-24 02:42:22 as ** along with 2 people jyuh ashandanj
  • In silico whole-genome scanning of cancer-associated nonsynonymous SNPs and molecular characterization of a dynein light chain tumour variant
    Oncogene, Vol. aop, No. current.
    by Abdel Aouacheria, Vincent Navratil, Wenyu Wen, Ming Jiang, Dominique Mouchiroud, Christian Gautier, Manolo Gouy, Mingjie Zhang, Mingjie Zhang
    posted to cancer nssnps by ramensky on 2008-08-31 14:32:24 as ** along with 1 person Ayest
  • Using protein complexes to predict phenotypic effects of gene mutation
    Genome Biology, Vol. 8 (27 November 2007), R252.
    by Hunter B Fraser, Joshua B Plotkin
    posted to nssnps protein-protein by ramensky on 2007-12-03 17:48:30 as ** along with 3 people grahamc jiny bpcusack
  • Balancing claims for balancing selection
    Trends in Genetics, Vol. 20, No. 7. (July 2004), pp. 300-304.
    by Martin Kreitman, Anna Di Rienzo
    posted to association_studies nssnps by ramensky on 2008-01-29 00:38:03 as **
  • Sequence-based prioritization of nonsynonymous single-nucleotide polymorphisms for the study of disease mutations.
    Am J Hum Genet, Vol. 81, No. 2. (August 2007), pp. 346-360.
    by R Jiang, H Yang, L Zhou, CC Kuo, F Sun, T Chen
    posted to nssnps by ramensky on 2008-01-22 23:00:08 as ** along with 1 person jyuh
  • Structural Location of Disease-associated Single-nucleotide Polymorphisms
    Journal of Molecular Biology, Vol. 327, No. 5. (11 April 2003), pp. 1021-1030.
    by Nathan O Stitziel, Yan Y Tseng, Dimitri Pervouchine, David Goddeau, Simon Kasif, Jie Liang
    posted to nssnps by ramensky on 2008-02-22 14:16:47 as **
  • The amino-acid mutational spectrum of human genetic disease.
    Genome Biol, Vol. 4, No. 11. (2003)
    by D Vitkup, C Sander, GM Church
    posted to association_studies nssnps by ramensky on 2007-10-01 18:42:35 as ** along with 2 people and 1 group koller cat_worth structural_bioinformatics
  • notes Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information.
    Bioinformatics (7 August 2006)
    by E Capriotti, R Calabrese, R Casadio
    posted to nssnps by ramensky on 2007-02-24 02:18:57 as **** along with 2 people and 1 group chad_davis OriginalLurch clab
  • Molecular basis of inherited diseases: a structural perspective.
    Trends Genet, Vol. 19, No. 9. (September 2003), pp. 505-513.
    by RE Steward, MW MacArthur, RA Laskowski, JM Thornton
    posted to 3d mutations nssnps by ramensky on 2007-10-23 21:09:13 as ** along with 2 people bicko chad_davis
  • Highly consistent patterns for inherited human diseases at the molecular level
    Bioinformatics, Vol. 22, No. 3. (1 February 2006), pp. 269-277.
    by Nuria Lopez-Bigas, Benjamin J Blencowe, Christos A Ouzounis
    posted to association_studies nssnps by ramensky on 2007-10-19 17:17:09 as ****
  • Screening for Deleterious Nonsynonymous Single-Nucleotide Polymorphisms in Genes Involved in Steroid Hormone Metabolism and Response
    Cancer Epidemiol Biomarkers Prev, Vol. 14, No. 5. (1 May 2005), pp. 1326-1329.
    by Melissa M Johnson, John Houck, Chu Chen
    posted to nssnps by ramensky on 2008-06-24 00:17:51 as ** along with 1 person Run7
  • Global variation in copy number in the human genome
    Nature, Vol. 444, No. 7118. (23 November 2006), pp. 444-454.
    by Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, Daniel T Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen, Eun K Cho, Stephanie Dallaire, Jennifer L Freeman, Juan R Gonzalez, Monica Gratacos, Jing Huang, Dimitrios Kalaitzopoulos, Daisuke Komura, Jeffrey R Macdonald, Christian R Marshall, Rui Mei, Lyndal Montgomery, Kunihiro Nishimura, Kohji Okamura, Fan Shen, Martin J Somerville, Joelle Tchinda, Armand Valsesia, Cara Woodwark, Fengtang Yang, Junjun Zhang, Tatiana Zerjal, Jane Zhang, Lluis Armengol, Donald F Conrad, Xavier Estivill, Chris Tyler-Smith, Nigel P Carter, Hiroyuki Aburatani, Charles Lee, Keith W Jones, Stephen W Scherer, Matthew E Hurles
    posted to evolution haplotypes misc nssnps by ramensky on 2007-06-17 16:30:18 as ** along with 27 people and 7 groups jo_davies psique bpb jfr balajis pradiptaray dpollard mtagaya adepace aswin rdiaz qfwills ealloza vplagnol giovanni jeremymiller frohike vpschulz raiyar ccr azazello dbgrant colinveal xingxu srp33 Ema daed parkinson's disease references Bioinformatics EisenLab BioinfoCIPF GeschwindLab steinmetzlab MBLAB
  • The complete genome of an individual by massively parallel DNA sequencing
    Nature, Vol. 452, No. 7189. (17 April 2008), pp. 872-876.
    by David A Wheeler, Maithreyan Srinivasan, Michael Egholm, Yufeng Shen, Lei Chen, Amy Mcguire, Wen He, Yi-Ju Chen, Vinod Makhijani, Thomas G Roth, Xavier Gomes, Karrie Tartaro, Faheem Niazi, Cynthia L Turcotte, Gerard P Irzyk, James R Lupski, Craig Chinault, Xing-Zhi Song, Yue Liu, Ye Yuan, Lynne Nazareth, Xiang Qin, Donna M Muzny, Marcel Margulies, George M Weinstock, Richard A Gibbs, Jonathan M Rothberg
    posted to nssnps by ramensky on 2008-04-20 15:49:08 as ** along with 14 people and 2 groups adijr jo_davies jfr orzenil dullhunk djkt psique caseybrown melting dbensasson bpb Neeperando Huub_odc jyuh parkinson's disease references microbiology_nijmegen
  • Natural selection of protein structural and functional properties: a SNP perspective
    Genome Biology, Vol. 9, No. 4. (2008)
    by Jinfeng Liu, Yan Zhang, Xingye Lei, Zemin Zhang
    posted to nssnps by ramensky on 2008-04-12 12:56:16 as ** along with 4 people and 1 group operon fernan stajich dandaman Berkeley Mycology
  • Medical sequencing at the extremes of human body mass.
    Am J Hum Genet, Vol. 80, No. 4. (April 2007), pp. 779-791.
    by N Ahituv, N Kavaslar, W Schackwitz, A Ustaszewska, J Martin, S Hebert, H Doelle, B Ersoy, G Kryukov, S Schmidt, N Yosef, E Ruppin, R Sharan, C Vaisse, S Sunyaev, R Dent, J Cohen, R McPherson, LA Pennacchio
    posted to association_studies nssnps by ramensky on 2007-05-28 20:39:10 as **** along with 2 people balicea lp2
  • Functional characterization of non-synonymous single nucleotide polymorphisms in the gene encoding human multidrug resistance protein 1 (MRP1/ABCC1).
    Pharmacogenet Genomics, Vol. 15, No. 9. (September 2005), pp. 647-657.
    by IJ Létourneau, RG Deeley, SP Cole
    posted to nssnps personalized_medicine by ramensky on 2008-06-23 22:42:29 as ** along with 1 person happy_manatee
  • Improving functional annotation of non-synonomous SNPs with information theory.
    Pac Symp Biocomput (2005), pp. 397-408.
    by R Karchin, L Kelly, A Sali
    posted to nssnps by ramensky on 2007-04-11 18:46:04 as ** along with 1 person happy_manatee
  • The Diploid Genome Sequence of an Individual Human
    PLoS Biology, Vol. 5, No. 10. (1 October 2007), e254.
    by Samuel Levy, Granger Sutton, Pauline C Ng, Lars Feuk, Aaron L Halpern, Brian P Walenz, Nelson Axelrod, Jiaqi Huang, Ewen F Kirkness, Gennady Denisov, Yuan Lin, Jeffrey R Macdonald, Andy W Pang, Mary Shago, Timothy B Stockwell, Alexia Tsiamouri, Vineet Bafna, Vikas Bansal, Saul A Kravitz, Dana A Busam, Karen Y Beeson, Tina C Mcintosh, Karin A Remington, Josep F Abril, John Gill, Jon Borman, Yu-Hui Rogers, Marvin E Frazier, Stephen W Scherer, Robert L Strausberg, Craig J Venter
    posted to haplotypes nssnps by ramensky on 2008-01-28 21:29:36 as ** along with 19 people and 1 group adijr Neeperando operon carlblesius bpb balicea skhadar dullhunk djkt jackjackjjj massivemayhem jasonbobe PredictER lp2 cabbagezs xingxu hpaces maburkitt nhp Bioinformatics
  • Direct estimation of per nucleotide and genomic deleterious mutation rates in Drosophila
    Nature, Vol. 445, No. 7123. (4 January 2007), pp. 82-85.
    by Cathy Haag-Liautard, Mark Dorris, Xulio Maside, Steven Macaskill, Daniel L Halligan, Brian Charlesworth, Peter D Keightley
    posted to evolution nssnps by ramensky on 2007-05-22 19:16:05 as *** along with 6 people and 1 group operon dpollard jri stajich lusk gjuggler EisenLab
  • Inflammatory bowel disease: Genetic and epidemiologic considerations.
    World J Gastroenterol, Vol. 14, No. 3. (21 January 2008), pp. 338-347.
    by JH Cho
    posted to association_studies nssnps by ramensky on 2008-02-01 18:19:23 as ** along with 1 person shikin
  • In silico prediction of the deleterious effect of a mutation: proceed with caution in clinical genetics.
    Clin Chem, Vol. 50, No. 11. (November 2004), pp. 1974-1978.
    by D Tchernitchko, M Goossens, H Wajcman
    posted to nssnps by ramensky on 2008-06-24 00:20:35 as ** along with 1 person chrn
  • Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism.
    Am J Hum Genet, Vol. 67, No. 4. (October 2000), pp. 881-900.
    by SM Fullerton, AG Clark, KM Weiss, DA Nickerson, SL Taylor, JH Stengârd, V Salomaa, E Vartiainen, M Perola, E Boerwinkle, CF Sing
    posted to association_studies haplotypes nssnps by ramensky on 2008-01-28 20:14:32 as **
  • Bioinformatics approaches and resources for single nucleotide polymorphism functional analysis.
    Brief Bioinform, Vol. 6, No. 1. (March 2005), pp. 44-56.
    by S Mooney
    posted to nssnps by ramensky on 2008-08-03 15:24:47 as ** along with 1 person and 2 groups indigoviolet Bioinformatics EisenLab
  • Proportionally more deleterious genetic variation in European than in African populations
    Nature, Vol. 451, No. 7181. (21 February 2008), pp. 994-997.
    by Kirk E Lohmueller, Amit R Indap, Steffen Schmidt, Adam R Boyko, Ryan D Hernandez, Melissa J Hubisz, John J Sninsky, Thomas J White, Shamil R Sunyaev, Rasmus Nielsen, Andrew G Clark, Carlos D Bustamante
    posted to association_studies nssnps by ramensky on 2008-07-04 14:19:18 as ** along with 3 people and 1 group djkt caseybrown mailund Fasting, food and evolution
  • Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms.
    Am J Hum Genet, Vol. 82, No. 1. (January 2008), pp. 100-112.
    by IP Gorlov, OY Gorlova, SR Sunyaev, MR Spitz, CI Amos
    posted to association_studies nssnps by ramensky on 2008-03-08 23:48:12 as ** along with 1 person jyuh
  • Population genetics models of common diseases
    Current Opinion in Genetics & Development, Vol. 16, No. 6. (December 2006), pp. 630-636.
    by Anna Di Rienzo
    posted to association_studies nssnps by ramensky on 2008-01-29 00:46:21 as ** along with 1 person ryanraaum
  • Assessing the function of genetic variants in candidate gene association studies
    Nat Rev Genet, Vol. 5, No. 8. (2004), pp. 589-597.
    by Timothy R Rebbeck, Margaret Spitz, Xifeng Wu
    posted to association_studies nssnps by ramensky on 2008-03-08 23:42:37 as ** along with 1 person raiyar
  • Predicting the Effects of Amino Acid Substitutions on Protein Function.
    Annu Rev Genomics Hum Genet (9 August 2005)
    by Pauline C C Ng, Steven Henikoff
    posted to nssnps by ramensky on 2007-07-19 17:07:38 as **** along with 6 people and 2 groups Einat caporaso hdopazo massivemayhem cat_worth lpfernandes structural_bioinformatics biomedical-nlp
  • Most rare missense alleles are deleterious in humans: implications for complex disease and association studies.
    Am J Hum Genet, Vol. 80, No. 4. (April 2007), pp. 727-739.
    by GV Kryukov, LA Pennacchio, SR Sunyaev
    posted to association_studies nssnps by ramensky on 2007-05-28 20:39:53 as ****
    • Вы можете ссылаться на эту страницу по адресу: http://www.citeulike.org/tag/nssnps

    RIS BibTeX
    CiteULike organises scholarly (or academic) papers or literature and provides bibliographic (which means it makes bibliographies) for universities and higher education establishments. It helps undergraduates and postgraduates. People studying for PhDs or in postdoctoral (postdoc) positions. The service is similar in scope to EndNote or RefWorks or any other reference manager like BibTeX, but it is a social bookmarking service for scientists and humanities researchers.