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Items: 1 to 20 of 221

1.

Gene sequencing. The race for the $1000 genome.

Service RF.

Science. 2006 Mar 17;311(5767):1544-6. No abstract available.

PMID:
16543431
2.

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 1;327(5961):78-81. doi: 10.1126/science.1181498. Epub 2009 Nov 5.

3.

DNA sequencing and genotyping.

Barron A.

Electrophoresis. 2008 Dec;29(23):4617. doi: 10.1002/elps.200890104. No abstract available.

PMID:
19053152
4.

Sequencing. Gels and genomes.

Rogers J.

Science. 1999 Oct 15;286(5439):429. No abstract available.

PMID:
10577205
5.

RIKEN integrated sequence analysis (RISA) system--384-format sequencing pipeline with 384 multicapillary sequencer.

Shibata K, Itoh M, Aizawa K, Nagaoka S, Sasaki N, Carninci P, Konno H, Akiyama J, Nishi K, Kitsunai T, Tashiro H, Itoh M, Sumi N, Ishii Y, Nakamura S, Hazama M, Nishine T, Harada A, Yamamoto R, Matsumoto H, Sakaguchi S, Ikegami T, Kashiwagi K, Fujiwake S, Inoue K, Togawa Y.

Genome Res. 2000 Nov;10(11):1757-71.

7.

Advantages and limitations of next-generation sequencing technologies: a comparison of electrophoresis and non-electrophoresis methods.

Hert DG, Fredlake CP, Barron AE.

Electrophoresis. 2008 Dec;29(23):4618-26. doi: 10.1002/elps.200800456. Review.

PMID:
19053153
8.

Multiplex amplification of large sets of human exons.

Porreca GJ, Zhang K, Li JB, Xie B, Austin D, Vassallo SL, LeProust EM, Peck BJ, Emig CJ, Dahl F, Gao Y, Church GM, Shendure J.

Nat Methods. 2007 Nov;4(11):931-6. Epub 2007 Oct 14.

PMID:
17934468
9.

Next-generation sequencing: the race is on.

von Bubnoff A.

Cell. 2008 Mar 7;132(5):721-3. doi: 10.1016/j.cell.2008.02.028.

10.
11.

DNA sequencing. No genome left behind.

Pennisi E.

Science. 2009 Nov 6;326(5954):794-5. doi: 10.1126/science.326_794. No abstract available.

PMID:
19892959
12.

Accurate multiplex polony sequencing of an evolved bacterial genome.

Shendure J, Porreca GJ, Reppas NB, Lin X, McCutcheon JP, Rosenbaum AM, Wang MD, Zhang K, Mitra RD, Church GM.

Science. 2005 Sep 9;309(5741):1728-32. Epub 2005 Aug 4.

13.

Hubris and the human genome.

Marshall E, Pennisi E.

Science. 1998 May 15;280(5366):994-5. No abstract available.

PMID:
9616087
14.
15.

Genomics: massively parallel sequencing.

Rogers YH, Venter JC.

Nature. 2005 Sep 15;437(7057):326-7. No abstract available.

PMID:
16163333
16.

[Critical parameters in clinical sequencing].

Jordan B.

Med Sci (Paris). 2012 Jan;28(1):109-11. doi: 10.1051/medsci/2012281025. Epub 2012 Jan 27. French. No abstract available.

17.

Microfluidic devices for DNA sequencing: sample preparation and electrophoretic analysis.

Paegel BM, Blazej RG, Mathies RA.

Curr Opin Biotechnol. 2003 Feb;14(1):42-50. Review.

PMID:
12566001
18.

Low-cost-medium throughput Sanger dideoxy sequencing.

Nielsen KL.

Methods Mol Biol. 2008;387:71-80.

PMID:
18287623
19.

Tech.Sight. Sequencing genomes and beyond.

Meldrum DR.

Science. 2001 Apr 20;292(5516):515-7. No abstract available.

PMID:
11330300
20.

Personal genome sequencing: the answer to all of our worries.

Nelkin D.

Hastings Cent Rep. 2003 Jan-Feb;33(1):9. No abstract available.

PMID:
12613377

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