Skip Navigation


Bioinformatics Advance Access originally published online on December 7, 2004
Bioinformatics 2005 21(8):1735-1736; doi:10.1093/bioinformatics/bti201
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (Print PDF) Freely available
Right arrow All Versions of this Article:
21/8/1735    most recent
bti201v1
Right arrow Comments: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Comments are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (16)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Ao, S. I.
Right arrow Articles by Sham, P. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ao, S. I.
Right arrow Articles by Sham, P. C.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2004. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions{at}oupjournals.org

CLUSTAG: hierarchical clustering and graph methods for selecting tag SNPs

S. I. Ao 1, Kevin Yip 2, Michael Ng 1,*, David Cheung 2, Pui-Yee Fong 3, Ian Melhado 3 and Pak C. Sham 3

1Department of Mathematics, The University of Hong Kong Pokfulam, Hong Kong
2Department of Computer Science, The University of Hong Kong Pokfulam, Hong Kong
3Genome Research Center, The University of Hong Kong Pokfulam, Hong Kong

*To whom correspondence should be addressed.

Summary: Cluster and set-cover algorithms are developed to obtain a set of tag single nucleotide polymorphisms (SNPs) that can represent all the known SNPs in a chromosomal region, subject to the constraint that all SNPs must have a squared correlation R2 > C with at least one tag SNP, where C is specified by the user.

Availability: http://hkumath.hku.hk/web/link/CLUSTAG/CLUSTAG.html

Contact: mng{at}maths.hku.hk


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Hum Mol GenetHome page
C.-L. Cheung, B. Y.Y. Chan, V. Chan, S. Ikegawa, I. Kou, H. Ngai, D. Smith, K. D.K. Luk, Q.-Y. Huang, S. Mori, et al.
Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible genetic association with bone mineral density variation
Hum. Mol. Genet., February 15, 2009; 18(4): 679 - 687.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
Y. Nannya, K. Taura, M. Kurokawa, S. Chiba, and S. Ogawa
Evaluation of genome-wide power of genetic association studies based on empirical data from the HapMap project
Hum. Mol. Genet., October 15, 2007; 16(20): 2494 - 2505.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
P. C. Sham, S. I. Ao, J. S. H. Kwan, P. Kao, F. Cheung, P. Y. Fong, and M. K. Ng
Combining functional and linkage disequilibrium information in the selection of tag SNPs
Bioinformatics, January 1, 2007; 23(1): 129 - 131.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.