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Items: 1 to 20 of 29

1.

Multiplex amplification of all coding sequences within 10 cancer genes by Gene-Collector.

Fredriksson S, Banér J, Dahl F, Chu A, Ji H, Welch K, Davis RW.

Nucleic Acids Res. 2007;35(7):e47. Epub 2007 Feb 22.

2.

The consensus coding sequences of human breast and colorectal cancers.

Sjöblom T, Jones S, Wood LD, Parsons DW, Lin J, Barber TD, Mandelker D, Leary RJ, Ptak J, Silliman N, Szabo S, Buckhaults P, Farrell C, Meeh P, Markowitz SD, Willis J, Dawson D, Willson JK, Gazdar AF, Hartigan J, Wu L, Liu C, Parmigiani G, Park BH, Bachman KE, Papadopoulos N, Vogelstein B, Kinzler KW, Velculescu VE.

Science. 2006 Oct 13;314(5797):268-74. Epub 2006 Sep 7.

3.

Unique features of a highly pathogenic Campylobacter jejuni strain.

Hofreuter D, Tsai J, Watson RO, Novik V, Altman B, Benitez M, Clark C, Perbost C, Jarvie T, Du L, Galán JE.

Infect Immun. 2006 Aug;74(8):4694-707. Erratum in: Infect Immun. 2007 Jan;75(1):542.

4.

Highly parallel genomic assays.

Fan JB, Chee MS, Gunderson KL.

Nat Rev Genet. 2006 Aug;7(8):632-44. Review.

PMID:
16847463
5.

A Sanger/pyrosequencing hybrid approach for the generation of high-quality draft assemblies of marine microbial genomes.

Goldberg SM, Johnson J, Busam D, Feldblyum T, Ferriera S, Friedman R, Halpern A, Khouri H, Kravitz SA, Lauro FM, Li K, Rogers YH, Strausberg R, Sutton G, Tallon L, Thomas T, Venter E, Frazier M, Venter JC.

Proc Natl Acad Sci U S A. 2006 Jul 25;103(30):11240-5. Epub 2006 Jul 13. Erratum in: Proc Natl Acad Sci U S A. 2006 Oct 24;103(43):16057.

6.

Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing.

Thomas RK, Nickerson E, Simons JF, Jänne PA, Tengs T, Yuza Y, Garraway LA, LaFramboise T, Lee JC, Shah K, O'Neill K, Sasaki H, Lindeman N, Wong KK, Borras AM, Gutmann EJ, Dragnev KH, DeBiasi R, Chen TH, Glatt KA, Greulich H, Desany B, Lubeski CK, Brockman W, Alvarez P, Hutchison SK, Leamon JH, Ronan MT, Turenchalk GS, Egholm M, Sellers WR, Rothberg JM, Meyerson M.

Nat Med. 2006 Jul;12(7):852-5. Epub 2006 Jun 25. Erratum in: Nat Med. 2006 Oct;12(10):1220.

PMID:
16799556
7.

Cancer genetics: colorectal cancer as a model.

Bodmer WF.

J Hum Genet. 2006;51(5):391-6. Epub 2006 Apr 5. Review.

8.

NIH Institutes launch joint venture to map cancer genome.

Vastag B.

J Natl Cancer Inst. 2006 Feb 1;98(3):162. No abstract available.

PMID:
16449675
9.

Analysis of P53 mutations and their expression in 56 colorectal cancer cell lines.

Liu Y, Bodmer WF.

Proc Natl Acad Sci U S A. 2006 Jan 24;103(4):976-81. Epub 2006 Jan 17.

10.

Support for the Human Cancer Genome Project.

Varmus H, Stillman B.

Science. 2005 Dec 9;310(5754):1615. No abstract available.

PMID:
16339428
11.

ProbeMaker: an extensible framework for design of sets of oligonucleotide probes.

Stenberg J, Nilsson M, Landegren U.

BMC Bioinformatics. 2005 Sep 19;6:229.

12.

Colorectal cancer: mutations in a signalling pathway.

Parsons DW, Wang TL, Samuels Y, Bardelli A, Cummins JM, DeLong L, Silliman N, Ptak J, Szabo S, Willson JK, Markowitz S, Kinzler KW, Vogelstein B, Lengauer C, Velculescu VE.

Nature. 2005 Aug 11;436(7052):792.

PMID:
16094359
13.

Multiplex PCR: use of heat-stable Thermus thermophilus RecA protein to minimize non-specific PCR products.

Shigemori Y, Mikawa T, Shibata T, Oishi M.

Nucleic Acids Res. 2005 Aug 8;33(14):e126.

14.

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.

15.

Genome sequencing in microfabricated high-density picolitre reactors.

Margulies M, Egholm M, Altman WE, Attiya S, Bader JS, Bemben LA, Berka J, Braverman MS, Chen YJ, Chen Z, Dewell SB, Du L, Fierro JM, Gomes XV, Godwin BC, He W, Helgesen S, Ho CH, Irzyk GP, Jando SC, Alenquer ML, Jarvie TP, Jirage KB, Kim JB, Knight JR, Lanza JR, Leamon JH, Lefkowitz SM, Lei M, Li J, Lohman KL, Lu H, Makhijani VB, McDade KE, McKenna MP, Myers EW, Nickerson E, Nobile JR, Plant R, Puc BP, Ronan MT, Roth GT, Sarkis GJ, Simons JF, Simpson JW, Srinivasan M, Tartaro KR, Tomasz A, Vogt KA, Volkmer GA, Wang SH, Wang Y, Weiner MP, Yu P, Begley RF, Rothberg JM.

Nature. 2005 Sep 15;437(7057):376-80. Epub 2005 Jul 31. Erratum in: Nature. 2006 May 4;441(7089):120. Ho, Chun He [corrected to Ho, Chun Heen].

16.

Toward genome-wide SNP genotyping.

Syvänen AC.

Nat Genet. 2005 Jun;37 Suppl:S5-10.

PMID:
15920530
17.

PieceMaker: selection of DNA fragments for selector-guided multiplex amplification.

Stenberg J, Dahl F, Landegren U, Nilsson M.

Nucleic Acids Res. 2005 Apr 28;33(8):e72.

18.

Multiplex amplification enabled by selective circularization of large sets of genomic DNA fragments.

Dahl F, Gullberg M, Stenberg J, Landegren U, Nilsson M.

Nucleic Acids Res. 2005 Apr 28;33(8):e71.

19.

NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins.

Pruitt KD, Tatusova T, Maglott DR.

Nucleic Acids Res. 2005 Jan 1;33(Database issue):D501-4.

20.

EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy.

Paez JG, Jänne PA, Lee JC, Tracy S, Greulich H, Gabriel S, Herman P, Kaye FJ, Lindeman N, Boggon TJ, Naoki K, Sasaki H, Fujii Y, Eck MJ, Sellers WR, Johnson BE, Meyerson M.

Science. 2004 Jun 4;304(5676):1497-500. Epub 2004 Apr 29.

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