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Items: 1 to 20 of 218

1.

Emulsion PCR-coupled target enrichment: an effective fishing method for high-throughput sequencing of poorly preserved ancient DNA.

Kihana M, Mizuno F, Sawafuji R, Wang L, Ueda S.

Gene. 2013 Oct 10;528(2):347-51. doi: 10.1016/j.gene.2013.07.040. Epub 2013 Jul 27.

PMID:
23900195
2.

Case study: enrichment of ancient mitochondrial DNA by hybridization capture.

Horn S.

Methods Mol Biol. 2012;840:189-95. doi: 10.1007/978-1-61779-516-9_22.

PMID:
22237536
3.

PCR-Free Enrichment of Mitochondrial DNA from Human Blood and Cell Lines for High Quality Next-Generation DNA Sequencing.

Gould MP, Bosworth CM, McMahon S, Grandhi S, Grimberg BT, LaFramboise T.

PLoS One. 2015 Oct 21;10(10):e0139253. doi: 10.1371/journal.pone.0139253. eCollection 2015. Erratum in: PLoS One. 2016 May 31;11(5):e0156884.

4.

Fast mitochondrial DNA isolation from mammalian cells for next-generation sequencing.

Quispe-Tintaya W, White RR, Popov VN, Vijg J, Maslov AY.

Biotechniques. 2013 Sep;55(3):133-6. doi: 10.2144/000114077.

5.

A high-throughput next-generation sequencing assay for the mitochondrial genome.

Dames S, Eilbeck K, Mao R.

Methods Mol Biol. 2015;1264:77-88. doi: 10.1007/978-1-4939-2257-4_8.

PMID:
25631005
6.

Targeted multiplex next-generation sequencing: advances in techniques of mitochondrial and nuclear DNA sequencing for population genomics.

Hancock-Hanser BL, Frey A, Leslie MS, Dutton PH, Archer FI, Morin PA.

Mol Ecol Resour. 2013 Mar;13(2):254-68. doi: 10.1111/1755-0998.12059. Epub 2013 Jan 25.

PMID:
23351075
7.

Performance evaluation of the next-generation sequencing approach for molecular diagnosis of hereditary hearing loss.

Sivakumaran TA, Husami A, Kissell D, Zhang W, Keddache M, Black AP, Tinkle BT, Greinwald JH Jr, Zhang K.

Otolaryngol Head Neck Surg. 2013 Jun;148(6):1007-16. doi: 10.1177/0194599813482294. Epub 2013 Mar 22.

PMID:
23525850
8.

Preparation of next-generation sequencing libraries from damaged DNA.

Briggs AW, Heyn P.

Methods Mol Biol. 2012;840:143-54. doi: 10.1007/978-1-61779-516-9_18.

PMID:
22237532
9.

Generating barcoded libraries for multiplex high-throughput sequencing.

Knapp M, Stiller M, Meyer M.

Methods Mol Biol. 2012;840:155-70. doi: 10.1007/978-1-61779-516-9_19.

PMID:
22237533
10.

High throughput HLA genotyping using 454 sequencing and the Fluidigm Access Array™ System for simplified amplicon library preparation.

Moonsamy PV, Williams T, Bonella P, Holcomb CL, Höglund BN, Hillman G, Goodridge D, Turenchalk GS, Blake LA, Daigle DA, Simen BB, Hamilton A, May AP, Erlich HA.

Tissue Antigens. 2013 Mar;81(3):141-9. doi: 10.1111/tan.12071.

PMID:
23398507
11.

[Current applications of high-throughput DNA sequencing technology in antibody drug research].

Yu X, Liu QG, Wang MR.

Yao Xue Xue Bao. 2012 Mar;47(3):322-31. Review. Chinese.

PMID:
22645755
12.
13.

Library construction for ancient genomics: single strand or double strand?

Bennett EA, Massilani D, Lizzo G, Daligault J, Geigl EM, Grange T.

Biotechniques. 2014 Jun 1;56(6):289-90, 292-6, 298, passim. doi: 10.2144/000114176. eCollection 2014 Jun.

14.

Performance evaluation of a mitogenome capture and Illumina sequencing protocol using non-probative, case-type skeletal samples: Implications for the use of a positive control in a next-generation sequencing procedure.

Marshall C, Sturk-Andreaggi K, Daniels-Higginbotham J, Oliver RS, Barritt-Ross S, McMahon TP.

Forensic Sci Int Genet. 2017 Nov;31:198-206. doi: 10.1016/j.fsigen.2017.09.001. Epub 2017 Sep 8.

15.

Analysis of high-throughput ancient DNA sequencing data.

Kircher M.

Methods Mol Biol. 2012;840:197-228. doi: 10.1007/978-1-61779-516-9_23.

PMID:
22237537
16.

Illumina sequencing library preparation for highly multiplexed target capture and sequencing.

Meyer M, Kircher M.

Cold Spring Harb Protoc. 2010 Jun;2010(6):pdb.prot5448. doi: 10.1101/pdb.prot5448.

PMID:
20516186
17.

Expanded genetic codes in next generation sequencing enable decontamination and mitochondrial enrichment.

McKernan KJ, Spangler J, Zhang L, Tadigotla V, McLaughlin S, Warner J, Zare A, Boles RG.

PLoS One. 2014 May 2;9(5):e96492. doi: 10.1371/journal.pone.0096492. eCollection 2014.

18.

Library preparation methods for next-generation sequencing: tone down the bias.

van Dijk EL, Jaszczyszyn Y, Thermes C.

Exp Cell Res. 2014 Mar 10;322(1):12-20. doi: 10.1016/j.yexcr.2014.01.008. Epub 2014 Jan 15. Review.

PMID:
24440557
19.

Single-stranded DNA library preparation for the sequencing of ancient or damaged DNA.

Gansauge MT, Meyer M.

Nat Protoc. 2013 Apr;8(4):737-48. doi: 10.1038/nprot.2013.038. Epub 2013 Mar 14.

PMID:
23493070
20.

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