Resolving the complexity of the human genome using single-molecule sequencing-Reference-Cited by-同舟云学术

Resolving the complexity of the human genome using single-molecule sequencing

Published:2014-11-10 Issue:7536 Volume:517 Page:608-611
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Chaisson Mark J. P.,Huddleston John,Dennis Megan Y.,Sudmant Peter H.,Malig Maika,Hormozdiari Fereydoun,Antonacci Francesca,Surti Urvashi,Sandstrom Richard,Boitano Matthew,Landolin Jane M.,Stamatoyannopoulos John A.,Hunkapiller Michael W.,Korlach Jonas,Eichler Evan E.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature13907.pdf

Reference27 articles.

1. The 1000 Genomes Project Consortium. An integrated map of genetic variation from 1,092 human genomes. Nature 491, 56–65 (2012)

2. The International HapMap Project Consortium. The International HapMap Project. Nature 426, 789–796 (2003)

3. International Human Genome Sequencing Consortium. Finishing the euchromatic sequence of the human genome. Nature 431, 931–945 (2004)

4. Kurahashi, H. et al. Molecular cloning of a translocation breakpoint hotspot in 22q11. Genome Res. 17, 461–469 (2007)

5. Genovese, G. et al. Using population admixture to help complete maps of the human genome. Nature Genet. 45, 406–414 (2013)

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