Multiplexed resequencing analysis to identify rare variants in pooled DNA with barcode indexing using next-generation sequencer-Reference-Cited by-同舟云学术

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Multiplexed resequencing analysis to identify rare variants in pooled DNA with barcode indexing using next-generation sequencer

Published:2010-05-20 Issue:7 Volume:55 Page:448-455
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Mitsui Jun,Fukuda Yoko,Azuma Kyo,Tozaki Hirokazu,Ishiura Hiroyuki,Takahashi Yuji,Goto Jun,Tsuji Shoji

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/jhg201046.pdf

Reference11 articles.

1. Altshuler, D., Daly, M. J. & Lander, E. S. Genetic mapping in human disease. Science 322, 881–888 (2008).

2. Frazer, K. A., Murray, S. S., Schork, N. J. & Topol, E. J. Human genetic variation and its contribution to complex traits. Nat. Rev. Genet. 10, 241–251 (2009).

3. Aharon-Peretz, J., Rosenbaum, H. & Gershoni-Baruch, R. Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews. N. Engl. J. Med. 351, 1972–1977 (2004).

4. Lwin, A., Orvisky, E., Goker-Alpan, O., LaMarca, M. E. & Sidransky, E. Glucocerebrosidase mutations in subjects with parkinsonism. Mol. Genet. Metab. 81, 70–73 (2004).

5. Mitsui, J., Mizuta, I., Toyoda, A., Ashida, R., Takahashi, Y., Goto, J. et al. Mutations for Gaucher disease confer high susceptibility to Parkinson disease. Arch. Neurol. 66, 571–576 (2009).

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