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所有的文献@标签 snp [719 articles]

当前文献的标签分类为: snp.
  • SNP-SNP interactions in breast cancer susceptibility.
    BMC cancer, Vol. 6 (2006)
    by VU Onay, L Briollais, JA Knight, E Shi, Y Wang, S Wells, H Li, I Rajendram, IL Andrulis, H Ozcelik
  • 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
  • notes New handles on genomic structural variation.
    Nature genetics, Vol. 40, No. 10. (October 2008)
    posted to variation snp review perspectives genomics cnv by Zephyrus on 2008-10-06 02:43:19 as **
  • Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer
    Nature Genetics, Vol. 40, No. 6. (27 April 2008), pp. 703-706.
    by Simon N Stacey, Andrei Manolescu, Patrick Sulem, Steinunn Thorlacius, Sigurjon A Gudjonsson, Gudbjörn F Jonsson, Margret Jakobsdottir, Jon T Bergthorsson, Julius Gudmundsson, Katja K Aben, Luc J Strobbe, Dorine W Swinkels, Anton KC van Engelenburg, Brian E Henderson, Laurence N Kolonel, Loic Le Marchand, Esther Millastre, Raquel Andres, Berta Saez, Julio Lambea, Javier Godino, Eduardo Polo, Alejandro Tres, Simone Picelli, Johanna Rantala, Sara Margolin, Thorvaldur Jonsson, Helgi Sigurdsson, Thora Jonsdottir, Jon Hrafnkelsson, Jakob Johannsson, Thorarinn Sveinsson, Gardar Myrdal, Hlynur N Grimsson, Steinunn G Sveinsdottir, Kristin Alexiusdottir, Jona Saemundsdottir, Asgeir Sigurdsson, Jelena Kostic, Larus Gudmundsson, Kristleifur Kristjansson, Gisli Masson, James D Fackenthal, Clement Adebamowo, Temidayo Ogundiran, Olufunmilayo I Olopade, Christopher A Haiman, Annika Lindblom, Jose I Mayordomo, Lambertus A Kiemeney, Jeffrey R Gulcher, Thorunn Rafnar, Unnur Thorsteinsdottir, Oskar T Johannsson, Augustine Kong, Kari Stefansson
  • From human genetics and genomics to pharmacogenetics and pharmacogenomics: past lessons, future directions.
    Drug metabolism reviews, Vol. 40, No. 2. (2008), pp. 187-224.
    by DW Nebert, G Zhang, ES Vesell
  • notes SNPs3D: Candidate gene and SNP selection for association studies
    BMC Bioinformatics, Vol. 7, No. 1. (2006)
    by Peng Yue, Eugene Melamud, John Moult
  • Letting the genome out of the bottle--will we get our wish?
    N Engl J Med, Vol. 358, No. 2. (10 January 2008), pp. 105-107.
    by DJ Hunter, MJ Khoury, JM Drazen
  • Allelic association and disease mapping.
    Brief Bioinform, Vol. 2, No. 4. (December 2001), pp. 375-387.
    posted to disease mapping snp by Yumyai on 2008-04-14 19:55:31 as *** along with 1 group Bioinformatics
  • Deleterious SNP prediction: be mindful of your training data!
    Bioinformatics, Vol. 23, No. 6. (15 March 2007), pp. 664-672.
  • Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA.
    Nature genetics (30 May 2008)
    by Lars G G Fritsche, Thomas Loenhardt, Andreas Janssen, Sheila A A Fisher, Andrea Rivera, Claudia N N Keilhauer, Bernhard H F H Weber
    posted to degeneration htra1 macular snp by ykaminoh on 2008-06-24 20:23:59 as **
  • Geography and genography: Prediction of continental origin using randomly selected single nucleotide polymorphisms
    BMC Genomics, Vol. 8 (10 March 2007), 68.
    by Dominic J Allocco, Qing Song, Gary H Gibbons, Marco F Ramoni, Isaac S Kohane
    posted to genography geography snp by yife on 2007-11-06 02:06:02 as ** along with 2 people fmacciardi pradiptaray
  • 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
  • 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
  • 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
  • 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
  • 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 **
  • 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
  • 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
  • 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
  • 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 Polymorphisms at Nucleotide Resolution with a Single DNA Microarray
    Science, Vol. 311, No. 5769. (31 March 2006), pp. 1932-1936.
    by David Gresham, Douglas M Ruderfer, Stephen C Pratt, Joseph Schacherer, Maitreya J Dunham, David Botstein, Leonid Kruglyak
  • 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
  • A genome-wide scalable SNP genotyping assay using microarray technology
    Nature Genetics, Vol. 37, No. 5. (17 April 2005), pp. 549-554.
    by Kevin L Gunderson, Frank J Steemers, Grace Lee, Leo G Mendoza, Mark S Chee
    posted to genomique snp by textoris on 2005-06-28 08:35:10 as ** along with 1 person pcahan1
  • Toward genome-wide SNP genotyping.
    Nat Genet, Vol. 37 Suppl (June 2005)
    by AC Syvänen
    posted to genomique snp by textoris on 2005-06-27 19:16:45 as ** along with 2 people BioGeek euphorium
  • Genome-wide association studies: theoretical and practical concerns
    Nature Reviews Genetics, Vol. 6, No. 2. (01 February 2005), pp. 109-118.
    by William YS Wang, Bryan J Barratt, David G Clayton, John A Todd
  • High-throughput SNP genotyping on universal bead arrays.
    Mutat Res, Vol. 573, No. 1-2. (3 June 2005), pp. 70-82.
    posted to application snp universal_microarrays by stsaft on 2007-03-27 05:46:21 as **
  • The next generation of microarray research: applications in evolutionary and ecological genomics
    Heredity, Vol. aop, No. current.
    by SH Shiu, JO Borevitz,
    posted to microarrays r21 review sfp snp by stsaft on 2008-06-11 00:24:27 as **
  • Calibrating the Performance of SNP Arrays for Whole-Genome Association Studies
    PLoS Genet, Vol. 4, No. 6. (27 June 2008), e1000109.
    by Ke Hao, Eric E Schadt, John D Storey
    posted to affy arrays association snp by Stew on 2008-07-07 08:45:06 as **** along with 4 people brianb caseybrown balicea jyuh
  • Linkage disequilibrium sharing and haplotype-tagged SNP portability between populations
    PNAS, Vol. 103, No. 5. (31 January 2006), pp. 1418-1421.
    by Wei Huang, Yungang He, Haifeng Wang, Ying Wang, Yangfan Liu, Yi Wang, Xun Chu, Ying Wang, Liang Xu, Yayun Shen, Xiaoyan Xiong, Hui Li, Bo Wen, Ji Qian, Wentao Yuan, Chenhui Zhang, Yi Wang, Hongquan Jiang, Guoping Zhao, Zhu Chen, Li Jin
    posted to linkage snp by stevanspringer on 2006-02-11 23:01:00 as ** along with 1 group FAB-lab
  • Genomic scans for selective sweeps using SNP data.
    Genome Res, Vol. 15, No. 11. (November 2005), pp. 1566-1575.
  • Human SNPs Reveal No Evidence of Frequent Positive Selection
    Mol Biol Evol, Vol. 22, No. 12. (1 December 2005), pp. 2504-2507.
    by Liqing Zhang, Wen-Hsiung Li
    posted to genome selection snp by stevanspringer on 2005-11-11 23:26:45 as ** along with 1 group FAB-lab
  • 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
  • Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays
    PLoS Genet, Vol. 4, No. 8. (2008), e1000167.
    by Nils Homer, Szabolcs Szelinger, Margot Redman, David Duggan, Waibhav Tembe, Jill Muehling, John V Pearson, Dietrich A Stephan, Stanley F Nelson, David W Craig
  • Immobilization of Protein Molecules onto Homogeneous and Mixed Carboxylate-Terminated Self-Assembled Monolayers
    Langmuir, Vol. 13, No. 24. (26 November 1997), pp. 6485-6490.
    by N Patel, MC Davies, M Hartshorne, RJ Heaton, CJ Roberts, SJB Tendler, PM Williams
    posted to 1 3 ausams protein_binding snp by sjanusz on 2007-08-14 12:48:33 as ****
  • Error detection in SNP data by considering the likelihood of recombinational history implied by three-site combinations.
    Bioinformatics (17 May 2007)
    by Donna M M Toleno, Peter L L Morrell, Michael T T Clegg
    posted to snp by shigepong on 2007-05-20 15:26:15 as *****
  • Quality scores and SNP detection in sequencing-by-synthesis systems
    Genome Res. (22 January 2008), gr.070227.107.
    by William Brockman, Pablo Alvarez, Sarah Young, Manuel Garber, Georgia Giannoukos, William L Lee, Carsten Russ, Eric S Lander, Chad Nusbaum, David B Jaffe
  • Consensus generation and variant detection by Celera Assembler.
    Bioinformatics (Oxford, England), Vol. 24, No. 8. (15 April 2008), pp. 1035-1040.
    by G Denisov, B Walenz, AL Halpern, J Miller, N Axelrod, S Levy, G Sutton
    posted to detection genome snp by semrich on 2008-07-05 21:50:18 as ***
  • WASP: a Web-based Allele-Specific PCR assay designing tool for detecting SNPs and mutations
    BMC Genomics, Vol. 8 (14 August 2007), 275.
    by Pongsakorn Wangkumhang, Kridsadakorn Chaichoompu, Chumpol Ngamphiw, Uttapong Ruangrit, Juntima Chanprasert, Anunchai Assawamakin, Sissades Tongsima
    posted to bioinformatics pcr snp software by sebastien_vigneau on 2008-04-03 00:16:27 as read along with 1 person jyuh
  • An efficient procedure for genotyping single nucleotide polymorphisms.
    Nucleic acids research, Vol. 29, No. 17. (1 September 2001)
    by S Ye, S Dhillon, X Ke, AR Collins, IN Day
    posted to bioinformatics pcr snp software by sebastien_vigneau on 2008-04-03 02:17:43 as **
  • Single-tube genotyping without oligonucleotide probes.
    Genome research, Vol. 9, No. 1. (January 1999), pp. 72-78.
    by S Germer, R Higuchi
    posted to genotyping pcr polymorphism snp technology by sebastien_vigneau on 2008-06-18 03:42:37 as **
  • The PCR suite.
    Bioinformatics, Vol. 20, No. 4. (1 March 2004), pp. 591-593.
    posted to pcr primer sequencing snp software by sebastien_vigneau on 2008-06-06 03:23:43 as read along with 1 person jyuh
  • High-throughput SNP genotyping by single-tube PCR with Tm-shift primers.
    BioTechniques, Vol. 39, No. 6. (December 2005), pp. 885-893.
    by J Wang, K Chuang, M Ahluwalia, S Patel, N Umblas, D Mirel, R Higuchi, S Germer
    posted to pcr polymorphism snp technology by sebastien_vigneau on 2008-06-18 03:40:10 as **
  • Screening of human SNP database identifies recoding sites of A-to-I RNA editing.
    RNA (New York, N.Y.) (4 September 2008)
    by Willemijn M M Gommans, Nicholas E E Tatalias, Christina P P Sie, Dylan Dupuis, Nicholas Vendetti, Lauren Smith, Rikhi Kaushal, Stefan Maas
    posted to snp sequencing rna editing by sebastien_vigneau on 2008-09-07 19:34:23 as **
  • Determination of allele frequency in pooled DNA: comparison of three PCR-based methods.
    BioTechniques, Vol. 39, No. 6. (December 2005), pp. 853-858.
    posted to genotyping pcr polymorphism qpcr snp technology by sebastien_vigneau on 2008-06-18 15:36:53 as read
  • SNPbox: web-based high-throughput primer design from gene to genome.
    Nucleic Acids Res, Vol. 32, No. Web Server issue. (1 July 2004)
  • Development of a real-time polymerase chain reaction-based method for the measurement of relative allelic expression and identification of CYP2A13 alleles with decreased expression in human lung.
    The Journal of pharmacology and experimental therapeutics, Vol. 311, No. 1. (October 2004), pp. 373-381.
    by X Zhang, M Caggana, TL Cutler, X Ding
    posted to cyp2a13 genotyping pcr polymorphism snp technology by sebastien_vigneau on 2008-06-18 03:37:38 as ***
  • Single nucleotide polymorphism genotyping using allele-specific PCR and fluorescence melting curves.
    BioTechniques, Vol. 34, No. 5. (May 2003), pp. 1068-1072.
    by AC Papp, JK Pinsonneault, G Cooke, W Sadée
    posted to pcr polymorphism snp technology by sebastien_vigneau on 2008-06-18 03:41:49 as ***
  • Melting curve analysis of SNPs (McSNP): a gel-free and inexpensive approach for SNP genotyping.
    BioTechniques, Vol. 30, No. 2. (February 2001)
    by JM Akey, D Sosnoski, E Parra, S Dios, K Hiester, B Su, C Bonilla, L Jin, MD Shriver
    posted to genotyping pcr polymorphism snp technology by sebastien_vigneau on 2008-06-18 03:36:02 as ****
  • A New Approach for Using Genome Scans to Detect Recent Positive Selection in the Human Genome.
    PLoS Biol, Vol. 5, No. 7. (19 June 2007)
    by Kun Tang, Kevin R R Thornton, Mark Stoneking
  • RTPrimerDB: the real-time PCR primer and probe database.
    Nucleic Acids Res, Vol. 31, No. 1. (1 January 2003), pp. 122-123.
    posted to pcr qpcr snp software by sebastien_vigneau on 2008-04-03 00:22:22 as read along with 1 person ecattell
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