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Items: 1 to 20 of 142

1.

Massively parallel sequencing: the next big thing in genetic medicine.

Tucker T, Marra M, Friedman JM.

Am J Hum Genet. 2009 Aug;85(2):142-54. doi: 10.1016/j.ajhg.2009.06.022. Review.

2.

Keeping up with the next generation: massively parallel sequencing in clinical diagnostics.

ten Bosch JR, Grody WW.

J Mol Diagn. 2008 Nov;10(6):484-92. doi: 10.2353/jmoldx.2008.080027. Epub 2008 Oct 2. Review.

3.

SNP detection for massively parallel whole-genome resequencing.

Li R, Li Y, Fang X, Yang H, Wang J, Kristiansen K, Wang J.

Genome Res. 2009 Jun;19(6):1124-32. doi: 10.1101/gr.088013.108. Epub 2009 May 6.

4.

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.

5.

Comprehensive next-generation cancer genome sequencing in the era of targeted therapy and personalized oncology.

Cronin M, Ross JS.

Biomark Med. 2011 Jun;5(3):293-305. doi: 10.2217/bmm.11.37. Review.

PMID:
21657839
6.

Massively parallel sequencing technology in pathogenic microbes.

Tripathy S, Jiang RH.

Methods Mol Biol. 2012;835:271-94. doi: 10.1007/978-1-61779-501-5_17.

PMID:
22183660
7.

Impacts of massively parallel sequencing for genetic diagnosis of neuromuscular disorders.

Vasli N, Laporte J.

Acta Neuropathol. 2013 Feb;125(2):173-85. doi: 10.1007/s00401-012-1072-7. Epub 2012 Dec 7. Review.

PMID:
23224362
8.

The development and impact of 454 sequencing.

Rothberg JM, Leamon JH.

Nat Biotechnol. 2008 Oct;26(10):1117-24. doi: 10.1038/nbt1485.

PMID:
18846085
9.

FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets.

Pope BJ, Nguyen-Dumont T, Odefrey F, Hammet F, Bell R, Tao K, Tavtigian SV, Goldgar DE, Lonie A, Southey MC, Park DJ.

BMC Bioinformatics. 2013 Feb 25;14:65. doi: 10.1186/1471-2105-14-65.

10.

[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
11.

Polymorphism discovery in high-throughput resequenced microarray-enriched human genomic loci.

Antipova AA, Sokolsky TD, Clouser CR, Dimalanta ET, Hendrickson CL, Kosnopo C, Lee CC, Ranade SS, Zhang L, Blanchard AP, McKernan KJ.

J Biomol Tech. 2009 Dec;20(5):253-7.

12.

Whole-exome/genome sequencing and genomics.

Grody WW, Thompson BH, Hudgins L.

Pediatrics. 2013 Dec;132(Suppl 3):S211-5. doi: 10.1542/peds.2013-1032E.

13.

Clinical application of massively parallel sequencing in the molecular diagnosis of glycogen storage diseases of genetically heterogeneous origin.

Wang J, Cui H, Lee NC, Hwu WL, Chien YH, Craigen WJ, Wong LJ, Zhang VW.

Genet Med. 2013 Feb;15(2):106-14. doi: 10.1038/gim.2012.104. Epub 2012 Aug 16.

PMID:
22899091
14.

What is next generation sequencing?

Behjati S, Tarpey PS.

Arch Dis Child Educ Pract Ed. 2013 Dec;98(6):236-8. doi: 10.1136/archdischild-2013-304340. Epub 2013 Aug 28. Review.

16.

Key principles and clinical applications of "next-generation" DNA sequencing.

Rizzo JM, Buck MJ.

Cancer Prev Res (Phila). 2012 Jul;5(7):887-900. doi: 10.1158/1940-6207.CAPR-11-0432. Epub 2012 May 22. Review.

17.

Whole-genome re-sequencing.

Bentley DR.

Curr Opin Genet Dev. 2006 Dec;16(6):545-52. Epub 2006 Oct 18. Review.

PMID:
17055251
18.

Implementing genomic medicine in pathology.

Williams ES, Hegde M.

Adv Anat Pathol. 2013 Jul;20(4):238-44. doi: 10.1097/PAP.0b013e3182977199. Review.

PMID:
23752086
19.

Next-generation DNA sequencing.

Shendure J, Ji H.

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

PMID:
18846087
20.

Approaches for classifying DNA variants found by Sanger sequencing in a medical genetics laboratory.

Cheong PL, Caramins M.

Methods Mol Biol. 2014;1168:227-50. doi: 10.1007/978-1-4939-0847-9_13. Review.

PMID:
24870139

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