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Items: 1 to 20 of 189

1.

The power of NGS technologies to delineate the genome organization in cancer: from mutations to structural variations and epigenetic alterations.

Schweiger MR, Kerick M, Timmermann B, Isau M.

Cancer Metastasis Rev. 2011 Jun;30(2):199-210. doi: 10.1007/s10555-011-9278-z. Review.

PMID:
21267768
2.

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
3.

Characterizing and interpreting genetic variation from personal genome sequencing.

Johansson AC, Feuk L.

Methods Mol Biol. 2012;838:343-67. doi: 10.1007/978-1-61779-507-7_17.

PMID:
22228021
4.

[Cancer genome analysis through next-generation sequencing].

Aburatani H.

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

PMID:
21368453
5.

Application of second-generation sequencing to cancer genomics.

Robison K.

Brief Bioinform. 2010 Sep;11(5):524-34. doi: 10.1093/bib/bbq013. Epub 2010 Apr 28. Review.

PMID:
20427421
6.

Whole cancer genome sequencing by next-generation methods.

Ross JS, Cronin M.

Am J Clin Pathol. 2011 Oct;136(4):527-39. doi: 10.1309/AJCPR1SVT1VHUGXW. Review.

PMID:
21917674
7.

Next generation sequencing in functional genomics.

Werner T.

Brief Bioinform. 2010 Sep;11(5):499-511. doi: 10.1093/bib/bbq018. Epub 2010 May 25. Review.

PMID:
20501549
8.

Next-generation sequencing.

Reis-Filho JS.

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

9.

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
10.

Advantages of next-generation sequencing versus the microarray in epigenetic research.

Hurd PJ, Nelson CJ.

Brief Funct Genomic Proteomic. 2009 May;8(3):174-83. doi: 10.1093/bfgp/elp013. Epub 2009 Jun 17. Review.

PMID:
19535508
11.

Next generation sequencing technologies in cancer diagnostics and therapeutics: A mini review.

Li W, Zhao K, Kirberger M, Liao W, Yan Y.

Cell Mol Biol (Noisy-le-grand). 2015 Oct 30;61(5):91-102. Review.

PMID:
26522064
12.

Next-generation sequencing and its applications in molecular diagnostics.

Su Z, Ning B, Fang H, Hong H, Perkins R, Tong W, Shi L.

Expert Rev Mol Diagn. 2011 Apr;11(3):333-43. doi: 10.1586/erm.11.3. Review.

PMID:
21463242
13.
14.

An integrative multi-dimensional genetic and epigenetic strategy to identify aberrant genes and pathways in cancer.

Chari R, Coe BP, Vucic EA, Lockwood WW, Lam WL.

BMC Syst Biol. 2010 May 17;4:67. doi: 10.1186/1752-0509-4-67.

15.

Functional genomics of cancer.

Liu ET.

Curr Opin Genet Dev. 2008 Jun;18(3):251-6. doi: 10.1016/j.gde.2008.07.014. Epub 2008 Aug 28. Review.

PMID:
18691651
16.

Epigenetic mapping and functional analysis in a breast cancer metastasis model using whole-genome promoter tiling microarrays.

Rodenhiser DI, Andrews J, Kennette W, Sadikovic B, Mendlowitz A, Tuck AB, Chambers AF.

Breast Cancer Res. 2008;10(4):R62. doi: 10.1186/bcr2121. Epub 2008 Jul 18.

17.

Massive parallel sequencing in animal genetics: wherefroms and wheretos.

PĂ©rez-Enciso M, Ferretti L.

Anim Genet. 2010 Dec;41(6):561-9. doi: 10.1111/j.1365-2052.2010.02057.x. Review.

PMID:
20477787
18.

Epigenetics and cancer, 2nd IARC meeting, Lyon, France, 6 and 7 December 2007.

Lambert MP, Herceg Z.

Mol Oncol. 2008 Jun;2(1):33-40. doi: 10.1016/j.molonc.2008.03.005. Epub 2008 Mar 27.

19.

The variation game: Cracking complex genetic disorders with NGS and omics data.

Cui H, Dhroso A, Johnson N, Korkin D.

Methods. 2015 Jun;79-80:18-31. doi: 10.1016/j.ymeth.2015.04.018. Epub 2015 May 2. Review.

PMID:
25944472
20.

Clinical application of amplicon-based next-generation sequencing in cancer.

Chang F, Li MM.

Cancer Genet. 2013 Dec;206(12):413-9. doi: 10.1016/j.cancergen.2013.10.003. Epub 2013 Oct 11. Review.

PMID:
24332266

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