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Results: 1 to 20 of 95

1.

DNA sequencing: clinical applications of new DNA sequencing technologies.

Dewey FE, Pan S, Wheeler MT, Quake SR, Ashley EA.

Circulation. 2012 Feb 21;125(7):931-44. doi: 10.1161/CIRCULATIONAHA.110.972828. No abstract available.

PMID:
22354974
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Massively parallel sequencing: the new frontier of hematologic genomics.

Johnsen JM, Nickerson DA, Reiner AP.

Blood. 2013 Nov 7;122(19):3268-75. doi: 10.1182/blood-2013-07-460287. Epub 2013 Sep 10. Review.

PMID:
24021669
[PubMed - indexed for MEDLINE]
3.

Genome structural variation discovery and genotyping.

Alkan C, Coe BP, Eichler EE.

Nat Rev Genet. 2011 May;12(5):363-76. doi: 10.1038/nrg2958. Epub 2011 Mar 1. Review.

PMID:
21358748
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Understanding human genetic variation in the era of high-throughput sequencing.

Knight JC.

EMBO Rep. 2010 Sep;11(9):650-2. doi: 10.1038/embor.2010.126. Epub 2010 Aug 20.

PMID:
20725090
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

A sample selection strategy for next-generation sequencing.

Kang CJ, Marjoram P.

Genet Epidemiol. 2012 Nov;36(7):696-709. doi: 10.1002/gepi.21664. Epub 2012 Aug 3.

PMID:
22865643
[PubMed - indexed for MEDLINE]
6.

The complete genome of an individual by massively parallel DNA sequencing.

Wheeler DA, Srinivasan M, Egholm M, Shen Y, Chen L, McGuire A, He W, Chen YJ, Makhijani V, Roth GT, Gomes X, Tartaro K, Niazi F, Turcotte CL, Irzyk GP, Lupski JR, Chinault C, Song XZ, Liu Y, Yuan Y, Nazareth L, Qin X, Muzny DM, Margulies M, Weinstock GM, Gibbs RA, Rothberg JM.

Nature. 2008 Apr 17;452(7189):872-6. doi: 10.1038/nature06884.

PMID:
18421352
[PubMed - indexed for MEDLINE]
7.

Two different high throughput sequencing approaches identify thousands of de novo genomic markers for the genetically depleted Bornean elephant.

Sharma R, Goossens B, Kun-Rodrigues C, Teixeira T, Othman N, Boone JQ, Jue NK, Obergfell C, O'Neill RJ, Chikhi L.

PLoS One. 2012;7(11):e49533. doi: 10.1371/journal.pone.0049533. Epub 2012 Nov 21. Erratum in: PLoS One. 2013;8(7). doi: 10.1371/annotation/8aaa2a9c-9c15-4214-808d-db8b0bd8ab88.

PMID:
23185354
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Comparison of sequencing platforms for single nucleotide variant calls in a human sample.

Ratan A, Miller W, Guillory J, Stinson J, Seshagiri S, Schuster SC.

PLoS One. 2013;8(2):e55089. doi: 10.1371/journal.pone.0055089. Epub 2013 Feb 6.

PMID:
23405114
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

A glimpse into past, present, and future DNA sequencing.

Morey M, Fernández-Marmiesse A, Castiñeiras D, Fraga JM, Couce ML, Cocho JA.

Mol Genet Metab. 2013 Sep-Oct;110(1-2):3-24. doi: 10.1016/j.ymgme.2013.04.024. Epub 2013 May 11. Review.

PMID:
23742747
[PubMed - indexed for MEDLINE]
10.

Identification and correction of systematic error in high-throughput sequence data.

Meacham F, Boffelli D, Dhahbi J, Martin DI, Singer M, Pachter L.

BMC Bioinformatics. 2011 Nov 21;12:451. doi: 10.1186/1471-2105-12-451.

PMID:
22099972
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

A method for discovery of genome-wide SNP between any two genotypes from whole-genome re-sequencing data.

Krishnan SG, Waters DL, Henry RJ.

Methods Mol Biol. 2014;1099:287-94. doi: 10.1007/978-1-62703-715-0_24.

PMID:
24243213
[PubMed - indexed for MEDLINE]
12.

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.

PMID:
19420381
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

New DNA sequencing technologies open a promising era for cancer research and treatment.

Sastre L.

Clin Transl Oncol. 2011 May;13(5):301-6. doi: 10.1007/s12094-011-0658-1. Review.

PMID:
21596657
[PubMed - indexed for MEDLINE]
14.

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]
15.

Sequencing technologies and genome sequencing.

Pareek CS, Smoczynski R, Tretyn A.

J Appl Genet. 2011 Nov;52(4):413-35. doi: 10.1007/s13353-011-0057-x. Epub 2011 Jun 23. Review.

PMID:
21698376
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Polymorphism ratio sequencing: a new approach for single nucleotide polymorphism discovery and genotyping.

Blazej RG, Paegel BM, Mathies RA.

Genome Res. 2003 Feb;13(2):287-93.

PMID:
12566407
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Recent patents on high-throughput single nucleotide polymorphism (SNP) genotyping methods.

de Paula Careta F, Paneto GG.

Recent Pat DNA Gene Seq. 2012 Aug;6(2):122-6. Review.

PMID:
22670603
[PubMed - indexed for MEDLINE]
18.

[Role of high-throughput sequencing in oncology].

Rodrigues MJ, Gomez-Roca C.

Bull Cancer. 2013 Mar;100(3):295-301. doi: 10.1684/bdc.2013.1717. Review. French.

PMID:
23501647
[PubMed - indexed for MEDLINE]
19.

Massively parallel sequencing approaches for characterization of structural variation.

Koboldt DC, Larson DE, Chen K, Ding L, Wilson RK.

Methods Mol Biol. 2012;838:369-84. doi: 10.1007/978-1-61779-507-7_18. Review.

PMID:
22228022
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Single-molecule sequencing of an individual human genome.

Pushkarev D, Neff NF, Quake SR.

Nat Biotechnol. 2009 Sep;27(9):847-50. doi: 10.1038/nbt.1561. Epub 2009 Aug 10.

PMID:
19668243
[PubMed - indexed for MEDLINE]
Free PMC Article

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