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Items: 1 to 20 of 159

1.

Does massively parallel DNA resequencing signify the end of histopathology as we know it?

Aparicio SA, Huntsman DG.

J Pathol. 2010 Jan;220(2):307-15. doi: 10.1002/path.2636. Review.

PMID:
19921711
2.

[Cancer genome analysis through next-generation sequencing].

Aburatani H.

Gan To Kagaku Ryoho. 2011 Jan;38(1):1-6. Review. Japanese.

PMID:
21368453
3.

Applications of next-generation sequencing technologies in functional genomics.

Morozova O, Marra MA.

Genomics. 2008 Nov;92(5):255-64. doi: 10.1016/j.ygeno.2008.07.001. Epub 2008 Aug 24. Review.

4.

An introduction to genes, genomes and disease.

Hall PA, Reis-Filho JS, Tomlinson IP, Poulsom R.

J Pathol. 2010 Jan;220(2):109-13. doi: 10.1002/path.2652.

PMID:
19960555
5.

Next-generation sequencing technologies for DNA methylation analyses in cancer genomics.

Boerno ST, Grimm C, Lehrach H, Schweiger MR.

Epigenomics. 2010 Apr;2(2):199-207. doi: 10.2217/epi.09.50. Review.

PMID:
22121870
6.

Next-generation sequencing: emerging lessons on the origins of human cancer.

Pfeifer GP, Hainaut P.

Curr Opin Oncol. 2011 Jan;23(1):62-8. doi: 10.1097/CCO.0b013e3283414d00. Review.

PMID:
21119514
7.

Next-generation sequencing.

Reis-Filho JS.

Breast Cancer Res. 2009;11 Suppl 3:S12. doi: 10.1186/bcr2431. Epub 2009 Dec 18.

8.

Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel Pyrosequencer.

Bordoni R, Bonnal R, Rizzi E, Carrera P, Benedetti S, Cremonesi L, Stenirri S, Colombo A, Montrasio C, Bonalumi S, Albertini A, Bernardi LR, Ferrari M, De Bellis G.

BMC Genomics. 2008 Oct 8;9:464. doi: 10.1186/1471-2164-9-464.

9.

[Human genome sequencing--next generation technology or will the routine sequencing of human genome be possible?].

Pospísilová S, Tichý B, Mayer J.

Cas Lek Cesk. 2009;148(7):296-302. Czech.

PMID:
19642294
10.

Deep sequencing in cancer research.

Yoshida K, Sanada M, Ogawa S.

Jpn J Clin Oncol. 2013 Feb;43(2):110-5. doi: 10.1093/jjco/hys206. Epub 2012 Dec 5. Review.

PMID:
23225907
11.

Single-molecule DNA sequencing technologies for future genomics research.

Gupta PK.

Trends Biotechnol. 2008 Nov;26(11):602-11. doi: 10.1016/j.tibtech.2008.07.003. Epub 2008 Aug 21. Review.

PMID:
18722683
12.

Targeted deep resequencing of the human cancer genome using next-generation technologies.

Myllykangas S, Ji HP.

Biotechnol Genet Eng Rev. 2010;27:135-58. Review.

13.

Generations of sequencing technologies.

Pettersson E, Lundeberg J, Ahmadian A.

Genomics. 2009 Feb;93(2):105-11. doi: 10.1016/j.ygeno.2008.10.003. Epub 2008 Nov 21. Review.

14.

Cancer genome sequencing and functional genomics: from translational to clinical medicine.

Roukos DH.

Pharmacogenomics. 2011 Oct;12(10):1371-4. doi: 10.2217/pgs.11.108. No abstract available.

PMID:
22008044
15.

Efficient targeted resequencing of human germline and cancer genomes by oligonucleotide-selective sequencing.

Myllykangas S, Buenrostro JD, Natsoulis G, Bell JM, Ji HP.

Nat Biotechnol. 2011 Oct 23;29(11):1024-7. doi: 10.1038/nbt.1996.

16.

Exome sequencing takes centre stage in cancer profiling.

Maher B.

Nature. 2009 May 14;459(7244):146-7. doi: 10.1038/459146b. No abstract available.

PMID:
19444175
17.

Exploring the genomes of cancer cells: progress and promise.

Stratton MR.

Science. 2011 Mar 25;331(6024):1553-8. doi: 10.1126/science.1204040. Review.

PMID:
21436442
19.

The clinical potential and challenges of sequencing cancer genomes for personalized medical genomics.

Cloonan N, Waddell N, Grimmond SM.

IDrugs. 2010 Nov;13(11):778-81. Review.

PMID:
21046525
20.

Next-generation DNA sequencing.

Shendure J, Ji H.

Nat Biotechnol. 2008 Oct;26(10):1135-45. doi: 10.1038/nbt1486.

PMID:
18846087

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