Skip Navigation



Bioinformatics Advance Access published online on June 28, 2007

Bioinformatics, doi:10.1093/bioinformatics/btm283
This Article
Right arrow Advance Access manuscript (PDF)
Right arrow All Versions of this Article:
23/15/1986    most recent
btm283v1
Right arrow Alert me when this article is cited
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 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 arrowRequest Permissions
Google Scholar
Right arrow Articles by Hu, J.
Right arrow Articles by Mills, G. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hu, J.
Right arrow Articles by Mills, G. B.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author (2007). Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Nonparametric Quantification of Protein Lysate Arrays

Jianhua Hu 1,*, Xuming He 2, Keith A. Baggerly 1, Kevin R. Coombes 1, Bryan T.J. Hennessy 3 and Gordon B. Mills 4

1Department of Bioinformatics and Computational Biology, 3Department of Gynecologic Medical Oncology, 4Department of Systems Biology, University of Texas M.D. Anderson Cancer Center.
2Department of Statistics, University of Illinois at Urbana-Champaign.

*To whom correspondence should be addressed. Prof. Jianhua Hu, E-mail: jhu{at}mdanderson.org


   Abstract

Motivation: Proteins play a crucial role in biological activity, so much can be learned from measuring protein expression and post-translational modification quantitatively. The Reverse-phase protein lysate arrays allow us to quantify the relative expression levels of a protein in many different cellular samples simultaneously. Existing approaches to quantify protein arrays use parametric response curves fit to dilution series data. The results can be biased when the parametric function does not fit the data.

Results: We propose a nonparametric approach which adapts to any monotone response curve. The nonparametric approach is shown to be promising via both simulation and real data studies; it reduces the bias due to model mis-specification and protects against outliers in the data. The nonparametric approach enables more reliable quantification of protein lysate arrays.

Availability: Code to implement the proposed method in the statistical package R is available at: http://odin.mdacc.tmc.edu/jhu/lysatearray-analysis/.

Associate Editor: Prof. John Quackenbush


Received on February 7, 2007; revised on April 10, 2007; accepted on May 19, 2007

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
BioinformaticsHome page
V. Vyshemirsky and M. A. Girolami
Bayesian ranking of biochemical system models
Bioinformatics, March 15, 2008; 24(6): 833 - 839.
[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.