Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?-Reference-Cited by-同舟云学术

Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?

Published:2014-03-26 Issue:1 Volume:23 Page:41-48
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Seneca Sara,Vancampenhout Kim,Van Coster Rudy,Smet Joél,Lissens Willy,Vanlander Arnaud,De Paepe Boel^ORCID,Jonckheere An,Stouffs Katrien,De Meirleir Linda

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg201449.pdf

Reference22 articles.

1. Schon EA, DiMauro S, Hirano M : Human mitochondrial DNA: roles of inherited and somatic mutations. Nat Rev Genet 2012; 13: 878–890.

2. Chinnery P, Hudson G : Mitochondrial genetics. Br Med Bull 2013; 106: 135–139.

3. MITOMAP: A Human Mitochondrial Genome Database. Available at: http://www.mitomap.org (last accessed 15 November 2013).

4. Naue J, Sänger T, Schmidt U, Klein R, Lutz-Bonengel S : Factors affecting the detection and quantification of mt point heteroplasmy using Sanger sequencing and SNaPshot minisequencing. Int J Legal Med 2011; 125: 427–436.

5. Metzker ML : Sequencing technologies – the next generation. Nat Rev Genet 2010; 11: 31–46.

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