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Journal Abstract Search
1092 related items for PubMed ID: 19892942
1. Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays. Drmanac R, Sparks AB, Callow MJ, Halpern AL, Burns NL, Kermani BG, Carnevali P, Nazarenko I, Nilsen GB, Yeung G, Dahl F, Fernandez A, Staker B, Pant KP, Baccash J, Borcherding AP, Brownley A, Cedeno R, Chen L, Chernikoff D, Cheung A, Chirita R, Curson B, Ebert JC, Hacker CR, Hartlage R, Hauser B, Huang S, Jiang Y, Karpinchyk V, Koenig M, Kong C, Landers T, Le C, Liu J, McBride CE, Morenzoni M, Morey RE, Mutch K, Perazich H, Perry K, Peters BA, Peterson J, Pethiyagoda CL, Pothuraju K, Richter C, Rosenbaum AM, Roy S, Shafto J, Sharanhovich U, Shannon KW, Sheppy CG, Sun M, Thakuria JV, Tran A, Vu D, Zaranek AW, Wu X, Drmanac S, Oliphant AR, Banyai WC, Martin B, Ballinger DG, Church GM, Reid CA. Science; 2010 Jan 01; 327(5961):78-81. PubMed ID: 19892942 [Abstract] [Full Text] [Related]
2. Gene sequencing. The race for the $1000 genome. Service RF. Science; 2006 Mar 17; 311(5767):1544-6. PubMed ID: 16543431 [No Abstract] [Full Text] [Related]
4. Preparation of genome-wide DNA fragment libraries using bisulfite in polyacrylamide gel electrophoresis slices with formamide denaturation and quality control for massively parallel sequencing by oligonucleotide ligation and detection. Ranade SS, Chung CB, Zon G, Boyd VL. Anal Biochem; 2009 Jul 15; 390(2):126-35. PubMed ID: 19379703 [Abstract] [Full Text] [Related]
5. A low-cost, high-throughput, automated single nucleotide polymorphism assay for forensic human DNA applications. Pomeroy R, Duncan G, Sunar-Reeder B, Ortenberg E, Ketchum M, Wasiluk H, Reeder D. Anal Biochem; 2009 Dec 01; 395(1):61-7. PubMed ID: 19646946 [Abstract] [Full Text] [Related]
6. SNP discovery and allele frequency estimation by deep sequencing of reduced representation libraries. Van Tassell CP, Smith TP, Matukumalli LK, Taylor JF, Schnabel RD, Lawley CT, Haudenschild CD, Moore SS, Warren WC, Sonstegard TS. Nat Methods; 2008 Mar 01; 5(3):247-52. PubMed ID: 18297082 [Abstract] [Full Text] [Related]
7. Single-molecule DNA sequencing of a viral genome. Harris TD, Buzby PR, Babcock H, Beer E, Bowers J, Braslavsky I, Causey M, Colonell J, Dimeo J, Efcavitch JW, Giladi E, Gill J, Healy J, Jarosz M, Lapen D, Moulton K, Quake SR, Steinmann K, Thayer E, Tyurina A, Ward R, Weiss H, Xie Z. Science; 2008 Apr 04; 320(5872):106-9. PubMed ID: 18388294 [Abstract] [Full Text] [Related]
8. Large-scale genotyping of complex DNA. Kennedy GC, Matsuzaki H, Dong S, Liu WM, Huang J, Liu G, Su X, Cao M, Chen W, Zhang J, Liu W, Yang G, Di X, Ryder T, He Z, Surti U, Phillips MS, Boyce-Jacino MT, Fodor SP, Jones KW. Nat Biotechnol; 2003 Oct 04; 21(10):1233-7. PubMed ID: 12960966 [Abstract] [Full Text] [Related]
9. Structural variation analysis with strobe reads. Ritz A, Bashir A, Raphael BJ. Bioinformatics; 2010 May 15; 26(10):1291-8. PubMed ID: 20378554 [Abstract] [Full Text] [Related]
10. Sequencing Medicago truncatula expressed sequenced tags using 454 Life Sciences technology. Cheung F, Haas BJ, Goldberg SM, May GD, Xiao Y, Town CD. BMC Genomics; 2006 Oct 24; 7():272. PubMed ID: 17062153 [Abstract] [Full Text] [Related]
11. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes]. Zhang DL, Ji L, Li YD. Yi Chuan Xue Bao; 2004 May 24; 31(5):431-43. PubMed ID: 15478601 [Abstract] [Full Text] [Related]
12. The $1000 genome: ethical and legal issues in whole genome sequencing of individuals. Robertson JA. Am J Bioeth; 2003 May 24; 3(3):W-IF1. PubMed ID: 14735880 [Abstract] [Full Text] [Related]
13. Next-generation sequencing methods: impact of sequencing accuracy on SNP discovery. Chan EY. Methods Mol Biol; 2009 May 24; 578():95-111. PubMed ID: 19768588 [Abstract] [Full Text] [Related]
14. 'PACLIMS': a component LIM system for high-throughput functional genomic analysis. Donofrio N, Rajagopalon R, Brown D, Diener S, Windham D, Nolin S, Floyd A, Mitchell T, Galadima N, Tucker S, Orbach MJ, Patel G, Farman M, Pampanwar V, Soderlund C, Lee YH, Dean RA. BMC Bioinformatics; 2005 Apr 12; 6():94. PubMed ID: 15826298 [Abstract] [Full Text] [Related]
15. The new paradigm of flow cell sequencing. Holt RA, Jones SJ. Genome Res; 2008 Jun 12; 18(6):839-46. PubMed ID: 18519653 [Abstract] [Full Text] [Related]
16. Perspectives and challenges of emerging single-molecule DNA sequencing technologies. Xu M, Fujita D, Hanagata N. Small; 2009 Dec 12; 5(23):2638-49. PubMed ID: 19904762 [Abstract] [Full Text] [Related]
17. New generation pharmacogenomic tools: a SNP linkage disequilibrium Map, validated SNP assay resource, and high-throughput instrumentation system for large-scale genetic studies. De La Vega FM, Dailey D, Ziegle J, Williams J, Madden D, Gilbert DA. Biotechniques; 2002 Jun 12; Suppl():48-50, 52, 54. PubMed ID: 12083398 [Abstract] [Full Text] [Related]
18. Direct selection of human genomic loci by microarray hybridization. Albert TJ, Molla MN, Muzny DM, Nazareth L, Wheeler D, Song X, Richmond TA, Middle CM, Rodesch MJ, Packard CJ, Weinstock GM, Gibbs RA. Nat Methods; 2007 Nov 12; 4(11):903-5. PubMed ID: 17934467 [Abstract] [Full Text] [Related]
19. Large-scale microfabricated channel plates for high-throughput, fully automated DNA sequencing. Kumagai H, Utsunomiya S, Nakamura S, Yamamoto R, Harada A, Kaji T, Hazama M, Ohashi T, Inami A, Ikegami T, Miyamoto K, Endo N, Yoshimi K, Toyoda A, Hattori M, Sakaki Y. Electrophoresis; 2008 Dec 12; 29(23):4723-32. PubMed ID: 19016243 [Abstract] [Full Text] [Related]
20. The Human Genome Project: lessons from large-scale biology. Collins FS, Morgan M, Patrinos A. Science; 2003 Apr 11; 300(5617):286-90. PubMed ID: 12690187 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]