Bioinformatics Advance Access originally published online on June 28, 2007
Bioinformatics 2007 23(15):1986-1994; doi:10.1093/bioinformatics/btm283
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Non-parametric quantification of protein lysate arrays
1Department of Bioinformatics and Computational Biology, University of Texas M.D. Anderson Cancer Center, 2Department of Statistics, University of Illinois at Urbana-Champaign, 3Department of Gynecologic Medical Oncology and 4Department of Systems Biology, University of Texas M.D. Anderson Cancer Center, USA
*To whom correspondence should be addressed.
| 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 non-parametric approach which adapts to any monotone response curve. The non-parametric approach is shown to be promising via both simulation and real data studies; it reduces the bias due to model misspecification and protects against outliers in the data. The non-parametric 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/
Contact: jhu{at}mdanderson.org
Supplementary information: Supplementary data are available at Bioinformatics online.
Associate Editor: John Quackenbush
Received on February 7, 2007; revised on April 10, 2007; accepted on May 19, 2007
This article has been cited by other articles:
![]() |
R. L. Dillon, R. Marcotte, B. T. Hennessy, J. R. Woodgett, G. B. Mills, and W. J. Muller Akt1 and Akt2 Play Distinct Roles in the Initiation and Metastatic Phases of Mammary Tumor Progression Cancer Res., June 15, 2009; 69(12): 5057 - 5064. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. S. Neeley, S. M. Kornblau, K. R. Coombes, and K. A. Baggerly Variable slope normalization of reverse phase protein arrays Bioinformatics, June 1, 2009; 25(11): 1384 - 1389. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Agarwal, A.-M. Gonzalez-Angulo, S. Myhre, M. Carey, J.-S. Lee, J. Overgaard, J. Alsner, K. Stemke-Hale, A. Lluch, R. M. Neve, et al. Integrative Analysis of Cyclin Protein Levels Identifies Cyclin B1 as a Classifier and Predictor of Outcomes in Breast Cancer Clin. Cancer Res., June 1, 2009; 15(11): 3654 - 3662. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. T. Hennessy, A.-M. Gonzalez-Angulo, K. Stemke-Hale, M. Z. Gilcrease, S. Krishnamurthy, J.-S. Lee, J. Fridlyand, A. Sahin, R. Agarwal, C. Joy, et al. Characterization of a Naturally Occurring Breast Cancer Subset Enriched in Epithelial-to-Mesenchymal Transition and Stem Cell Characteristics Cancer Res., May 15, 2009; 69(10): 4116 - 4124. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Chen, N. Guggisberg, M. Jorda, A. Gonzalez-Angulo, B. Hennessy, G. B. Mills, C.-K. Tan, and J. M. Slingerland Combined Src and Aromatase Inhibition Impairs Human Breast Cancer Growth In vivo and Bypass Pathways Are Activated in AZD0530-Resistant Tumors Clin. Cancer Res., May 15, 2009; 15(10): 3396 - 3405. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. M. Gonzalez-Angulo, K. Stemke-Hale, S. L. Palla, M. Carey, R. Agarwal, F. Meric-Berstam, T. A. Traina, C. Hudis, G. N. Hortobagyi, W. L. Gerald, et al. Androgen Receptor Levels and Association with PIK3CA Mutations and Prognosis in Breast Cancer Clin. Cancer Res., April 1, 2009; 15(7): 2472 - 2478. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. A. Nikolova, I. A. Asangani, L. D. Nelson, D. P.M. Hughes, D. R. Siwak, G. B. Mills, A. Harms, E. Buchholz, L. R. Pilz, C. Manegold, et al. Cetuximab Attenuates Metastasis and u-PAR Expression in Non-Small Cell Lung Cancer: u-PAR and E-Cadherin are Novel Biomarkers of Cetuximab Sensitivity Cancer Res., March 15, 2009; 69(6): 2461 - 2470. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Zhang, Q. Wei, L. Mao, W. Liu, G. B. Mills, and K. Coombes Serial dilution curve: a new method for analysis of reverse phase protein array data Bioinformatics, March 1, 2009; 25(5): 650 - 654. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. T. Ihle, R. Lemos Jr., P. Wipf, A. Yacoub, C. Mitchell, D. Siwak, G. B. Mills, P. Dent, D. L. Kirkpatrick, and G. Powis Mutations in the Phosphatidylinositol-3-Kinase Pathway Predict for Antitumor Activity of the Inhibitor PX-866 whereas Oncogenic Ras Is a Dominant Predictor for Resistance Cancer Res., January 1, 2009; 69(1): 143 - 150. [Abstract] [Full Text] [PDF] |
||||
![]() |
W.-Y. Kim, D. J. Chang, B. Hennessy, H. J. Kang, J. Yoo, S.-H. Han, Y.-S. Kim, H.-J. Park, S.-Y. Geo, G. Mills, et al. A Novel Derivative of the Natural Agent Deguelin for Cancer Chemoprevention and Therapy Cancer Prevention Research, December 1, 2008; 1(7): 577 - 587. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Vyshemirsky and M. A. Girolami Bayesian ranking of biochemical system models Bioinformatics, March 15, 2008; 24(6): 833 - 839. [Abstract] [Full Text] [PDF] |
||||



