Identification of genetic variants using bar-coded multiplexed sequencing-Reference-Cited by-同舟云学术

Identification of genetic variants using bar-coded multiplexed sequencing

Published:2008-09-14 Issue:10 Volume:5 Page:887-893
ISSN:1548-7091
Container-title:Nature Methods
language:en
Short-container-title:Nat Methods

Author:

Craig David W,Pearson John V,Szelinger Szabolcs,Sekar Aswin,Redman Margot,Corneveaux Jason J,Pawlowski Traci L,Laub Trisha,Nunn Gary,Stephan Dietrich A,Homer Nils,Huentelman Matthew J

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,Biochemistry,Biotechnology

Link

http://www.nature.com/articles/nmeth.1251.pdf

Reference13 articles.

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2. Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447, 661–678 (2007).

3. Zondervan, K.T. & Cardon, L.R. Designing candidate gene and genome-wide case-control association studies. Nat. Protoc. 2, 2492–2501 (2007).

4. Meyer, M., Stenzel, U., Myles, S., Prüfer, K. & Hofreiter, M. Targeted high-throughput sequencing of tagged nucleic acid samples. Nucleic Acids Res. 35, e97 (2007).

5. Parameswaran, P. et al. A pyrosequencing-tailored nucleotide barcode design unveils opportunities for large-scale sample multiplexing. Nucleic Acids Res. 35, e130 (2007).

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