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Results: 1 to 20 of 94

1.

Interpreting whole-genome sequencing--reply.

Dewey F, Ashley E, Quertermous T.

JAMA. 2014 Jul 16;312(3):296-7. doi: 10.1001/jama.2014.6605. No abstract available.

PMID:
25027152
[PubMed - indexed for MEDLINE]
2.

Interpreting whole-genome sequencing.

Grody WW, Vilain E, Nelson SF.

JAMA. 2014 Jul 16;312(3):296. doi: 10.1001/jama.2014.6602. No abstract available.

PMID:
25027151
[PubMed - indexed for MEDLINE]
3.

Clinical application of whole-genome sequencing: proceed with care.

Feero WG.

JAMA. 2014 Mar 12;311(10):1017-9. doi: 10.1001/jama.2014.1718. No abstract available.

PMID:
24618961
[PubMed - indexed for MEDLINE]
4.

[What contribution makes DNA sequencing in clinical practice? - before widespread application DNA sequencing has to be optimized].

Blum HE.

Dtsch Med Wochenschr. 2014 May;139(18):932. doi: 10.1055/s-0033-1353901. Epub 2014 Apr 23. German. No abstract available.

PMID:
24760713
[PubMed - indexed for MEDLINE]
5.

Pharmacogenomics for tailoring cardiovascular and anticancer drugs: from genotyping to whole-genome sequencing.

Katsios CS, Ziogas DE, Roukos DH.

Pharmacogenomics. 2011 Aug;12(8):1081-5. doi: 10.2217/pgs.11.58. No abstract available.

PMID:
21843060
[PubMed - indexed for MEDLINE]
6.

Opportunities and challenges for genome sequencing in the clinic.

Cavalleri GL, Delanty N.

Adv Protein Chem Struct Biol. 2012;89:65-83. doi: 10.1016/B978-0-12-394287-6.00003-3. Review.

PMID:
23046882
[PubMed - indexed for MEDLINE]
7.

Advances in understanding cancer genomes through second-generation sequencing.

Meyerson M, Gabriel S, Getz G.

Nat Rev Genet. 2010 Oct;11(10):685-96. doi: 10.1038/nrg2841. Review.

PMID:
20847746
[PubMed - indexed for MEDLINE]
8.

Clinical application of whole exome sequencing: not (yet) ready for primetime.

Sutton AL, Robin NH.

Curr Opin Pediatr. 2012 Dec;24(6):663-4. doi: 10.1097/MOP.0b013e32835a1996. No abstract available.

PMID:
23080129
[PubMed - indexed for MEDLINE]
9.

[Whole-genome sequencing: a new approach for understanding of pathogenesis and individualized treatment of cancer].

Pan Y, Zhang W, Chen S.

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2013 Jan;42(1):103-8. Review. Chinese.

PMID:
23505116
[PubMed - indexed for MEDLINE]
10.

Exome sequencing: the sweet spot before whole genomes.

Teer JK, Mullikin JC.

Hum Mol Genet. 2010 Oct 15;19(R2):R145-51. doi: 10.1093/hmg/ddq333. Epub 2010 Aug 12. Review.

PMID:
20705737
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Emerging DNA sequencing technologies for human genomic medicine.

Strausberg RL, Levy S, Rogers YH.

Drug Discov Today. 2008 Jul;13(13-14):569-77. doi: 10.1016/j.drudis.2008.03.025. Epub 2008 May 22. Review.

PMID:
18598911
[PubMed - indexed for MEDLINE]
12.

DREAMing of a patent-free human genome for clinical sequencing.

McKernan KJ, Spangler J, Helbert Y, Zhang L, Tadigotla V.

Nat Biotechnol. 2013 Oct;31(10):884-7. doi: 10.1038/nbt.2703. No abstract available.

PMID:
24104751
[PubMed - indexed for MEDLINE]
13.

Comprehensive characterization of human genome variation by high coverage whole-genome sequencing of forty four Caucasians.

Shen H, Li J, Zhang J, Xu C, Jiang Y, Wu Z, Zhao F, Liao L, Chen J, Lin Y, Tian Q, Papasian CJ, Deng HW.

PLoS One. 2013;8(4):e59494. doi: 10.1371/journal.pone.0059494. Epub 2013 Apr 5.

PMID:
23577066
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.

van El CG, Cornel MC, Borry P, Hastings RJ, Fellmann F, Hodgson SV, Howard HC, Cambon-Thomsen A, Knoppers BM, Meijers-Heijboer H, Scheffer H, Tranebjaerg L, Dondorp W, de Wert GM; ESHG Public and Professional Policy Committee.

Eur J Hum Genet. 2013 Jun;21(6):580-4. doi: 10.1038/ejhg.2013.46. No abstract available.

PMID:
23676617
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Enrichment of sequencing targets from the human genome by solution hybridization.

Tewhey R, Nakano M, Wang X, Pabón-Peña C, Novak B, Giuffre A, Lin E, Happe S, Roberts DN, LeProust EM, Topol EJ, Harismendy O, Frazer KA.

Genome Biol. 2009;10(10):R116. doi: 10.1186/gb-2009-10-10-r116. Epub 2009 Oct 16.

PMID:
19835619
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Genome sequencing and assembly.

Grabherr MG, Mauceli E, Ma LJ.

Methods Mol Biol. 2011;722:1-9. doi: 10.1007/978-1-61779-040-9_1.

PMID:
21590409
[PubMed - indexed for MEDLINE]
17.

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
[PubMed - indexed for MEDLINE]
18.

Genome sequencing on nanoballs.

Porreca GJ.

Nat Biotechnol. 2010 Jan;28(1):43-4. doi: 10.1038/nbt0110-43. No abstract available.

PMID:
20062041
[PubMed - indexed for MEDLINE]
19.

Whole exome sequencing.

Glass DA 2nd, Nuara AA.

Dermatitis. 2013 Jan-Feb;24(1):33-4. doi: 10.1097/DER.0b013e3182759e43.

PMID:
23340397
[PubMed - indexed for MEDLINE]
20.

Completely phased genome sequencing through chromosome sorting.

Yang H, Chen X, Wong WH.

Proc Natl Acad Sci U S A. 2011 Jan 4;108(1):12-7. doi: 10.1073/pnas.1016725108. Epub 2010 Dec 15. Erratum in: Proc Natl Acad Sci U S A. 2012 Feb 21;109(8):3190.

PMID:
21169219
[PubMed - indexed for MEDLINE]
Free PMC Article

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