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Items: 1 to 20 of 208

1.

Clinical Genomics: Challenges and Opportunities.

Vijay P, McIntyre AB, Mason CE, Greenfield JP, Li S.

Crit Rev Eukaryot Gene Expr. 2016;26(2):97-113. doi: 10.1615/CritRevEukaryotGeneExpr.2016015724. Review.

2.

Next generation sequencing in cancer: opportunities and challenges for precision cancer medicine.

Paolillo C, Londin E, Fortina P.

Scand J Clin Lab Invest Suppl. 2016;245:S84-91. doi: 10.1080/00365513.2016.1210331. Epub 2016 Aug 17.

PMID:
27542004
3.

An Overview of DNA Analytical Methods.

Arboleda VA, Xian RR.

Methods Mol Biol. 2019;1897:385-402. doi: 10.1007/978-1-4939-8935-5_31. Review.

PMID:
30539459
4.

Opportunities and challenges of whole-genome and -exome sequencing.

Petersen BS, Fredrich B, Hoeppner MP, Ellinghaus D, Franke A.

BMC Genet. 2017 Feb 14;18(1):14. doi: 10.1186/s12863-017-0479-5. Review.

5.

Clinical pharmacogenomics testing in the era of next generation sequencing: challenges and opportunities for precision medicine.

Ji Y, Si Y, McMillin GA, Lyon E.

Expert Rev Mol Diagn. 2018 May;18(5):411-421. doi: 10.1080/14737159.2018.1461561. Epub 2018 Apr 23. Review.

PMID:
29634383
6.

Next generation sequencing: implications in personalized medicine and pharmacogenomics.

Rabbani B, Nakaoka H, Akhondzadeh S, Tekin M, Mahdieh N.

Mol Biosyst. 2016 May 24;12(6):1818-30. doi: 10.1039/c6mb00115g. Review.

PMID:
27066891
7.

High-throughput sequencing technologies.

Reuter JA, Spacek DV, Snyder MP.

Mol Cell. 2015 May 21;58(4):586-97. doi: 10.1016/j.molcel.2015.05.004. Review.

8.

Next-generation sequencing in the clinic: promises and challenges.

Xuan J, Yu Y, Qing T, Guo L, Shi L.

Cancer Lett. 2013 Nov 1;340(2):284-95. doi: 10.1016/j.canlet.2012.11.025. Epub 2012 Nov 19. Review.

9.

Ten years of next-generation sequencing technology.

van Dijk EL, Auger H, Jaszczyszyn Y, Thermes C.

Trends Genet. 2014 Sep;30(9):418-26. doi: 10.1016/j.tig.2014.07.001. Epub 2014 Aug 6. Review.

PMID:
25108476
10.

Genomic Analysis of Childhood Brain Tumors: Methods for Genome-Wide Discovery and Precision Medicine Become Mainstream.

Mack SC, Northcott PA.

J Clin Oncol. 2017 Jul 20;35(21):2346-2354. doi: 10.1200/JCO.2017.72.9921. Epub 2017 Jun 22. Review.

PMID:
28640705
11.

Lake Louise mutation detection meeting 2013: clinical translation of next-generation sequencing requires optimization of workflows and interpretation of variants.

Smith A, Boycott KM, Jarinova O.

Hum Mutat. 2014 Feb;35(2):265-9. doi: 10.1002/humu.22480. Epub 2013 Nov 27.

PMID:
24282140
12.

A comparative study of k-spectrum-based error correction methods for next-generation sequencing data analysis.

Akogwu I, Wang N, Zhang C, Gong P.

Hum Genomics. 2016 Jul 25;10 Suppl 2:20. doi: 10.1186/s40246-016-0068-0.

13.

Controversy and debate on clinical genomics sequencing-paper 1: genomics is not exceptional: rigorous evaluations are necessary for clinical applications of genomic sequencing.

Wilson BJ, Miller FA, Rousseau F.

J Clin Epidemiol. 2017 Dec;92:4-6. doi: 10.1016/j.jclinepi.2017.08.018. Epub 2017 Sep 1. Review.

PMID:
28870871
14.

A comparative assessment of clinical whole exome and transcriptome profiling across sequencing centers: implications for precision cancer medicine.

Van Allen EM, Robinson D, Morrissey C, Pritchard C, Imamovic A, Carter S, Rosenberg M, McKenna A, Wu YM, Cao X, Chinnaiyan A, Garraway L, Nelson PS.

Oncotarget. 2016 Aug 16;7(33):52888-52899. doi: 10.18632/oncotarget.9184.

15.

Microarray and next-generation sequencing to analyse gastric cancer.

Dang Y, Wang YC, Huang QJ.

Asian Pac J Cancer Prev. 2014;15(19):8033-9. Review.

16.

Clinical tumor sequencing: opportunities and challenges for precision cancer medicine.

Damodaran S, Berger MF, Roychowdhury S.

Am Soc Clin Oncol Educ Book. 2015:e175-82. doi: 10.14694/EdBook_AM.2015.35.e175. Review.

17.

Exploiting the potential of next-generation sequencing in genomic medicine.

Pinto AM, Ariani F, Bianciardi L, Daga S, Renieri A.

Expert Rev Mol Diagn. 2016 Sep;16(9):1037-47. doi: 10.1080/14737159.2016.1224181. Review.

PMID:
27574853
18.

Analysis and annotation of whole-genome or whole-exome sequencing-derived variants for clinical diagnosis.

Worthey EA.

Curr Protoc Hum Genet. 2013 Oct 18;79:Unit 9.24.. doi: 10.1002/0471142905.hg0924s79.

PMID:
24510652
19.

Analyzing the cancer methylome through targeted bisulfite sequencing.

Lee EJ, Luo J, Wilson JM, Shi H.

Cancer Lett. 2013 Nov 1;340(2):171-8. doi: 10.1016/j.canlet.2012.10.040. Epub 2012 Nov 28. Review.

20.

Application of next generation sequencing to human gene fusion detection: computational tools, features and perspectives.

Wang Q, Xia J, Jia P, Pao W, Zhao Z.

Brief Bioinform. 2013 Jul;14(4):506-19. doi: 10.1093/bib/bbs044. Epub 2012 Aug 9. Review.

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