IDEAS home Printed from https://ideas.repec.org/a/eee/csdana/v53y2009i5p1743-1754.html
   My bibliography  Save this article

Simple Bayesian binary framework for discovering significant genes and classifying cancer diagnosis

Author

Listed:
  • Yang, Tae Young

Abstract

Given a microarray dataset consisting of two classes, type I and type II, the proposed coherent binary framework sequentially combines a gene-rank algorithm and a classifier. Genes that are expressed at a consistently high level in one type and at a consistently low level in the other type are of much interest. The wider the gap between the expression levels, the more significant the gene is as a discriminator. A new distance metric is used to measure the gap and is obtained using Bayesian nonparametric approaches involving Dirichlet process priors. Significant genes are ranked separately based on the pattern (the genes are over-expressed in type I and under-expressed in type II) or the pattern (the genes are under-expressed in type I and over-expressed in type II). An out-of-sample cross-validation approach is suggested for use in deciding how many significant genes are necessary for the classifier. The classifier uses each selected top-ranked gene to calculate a classification score when a test sample is presented. The sample is then classified as having the type with the larger score. Empirical studies using two public datasets show that top-ranked genes in each pattern clearly distinguish the existing pattern, and the classifier uses a few significant genes to classify the types in the test samples correctly. The framework is a simple, easy alternative to more complex models in terms of its accuracy and robustness.

Suggested Citation

  • Yang, Tae Young, 2009. "Simple Bayesian binary framework for discovering significant genes and classifying cancer diagnosis," Computational Statistics & Data Analysis, Elsevier, vol. 53(5), pages 1743-1754, March.
  • Handle: RePEc:eee:csdana:v:53:y:2009:i:5:p:1743-1754
    as

    Download full text from publisher

    File URL: http://www.sciencedirect.com/science/article/pii/S0167-9473(08)00213-2
    Download Restriction: Full text for ScienceDirect subscribers only.
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    References listed on IDEAS

    as
    1. Dudoit S. & Fridlyand J. & Speed T. P, 2002. "Comparison of Discrimination Methods for the Classification of Tumors Using Gene Expression Data," Journal of the American Statistical Association, American Statistical Association, vol. 97, pages 77-87, March.
    2. Geman Donald & d'Avignon Christian & Naiman Daniel Q. & Winslow Raimond L., 2004. "Classifying Gene Expression Profiles from Pairwise mRNA Comparisons," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 3(1), pages 1-22, August.
    3. Lee, Jae Won & Lee, Jung Bok & Park, Mira & Song, Seuck Heun, 2005. "An extensive comparison of recent classification tools applied to microarray data," Computational Statistics & Data Analysis, Elsevier, vol. 48(4), pages 869-885, April.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Hossain, Ahmed & Beyene, Joseph & Willan, Andrew R. & Hu, Pingzhao, 2009. "A flexible approximate likelihood ratio test for detecting differential expression in microarray data," Computational Statistics & Data Analysis, Elsevier, vol. 53(10), pages 3685-3695, August.
    2. Alan R Dabney & John D Storey, 2007. "Optimality Driven Nearest Centroid Classification from Genomic Data," PLOS ONE, Public Library of Science, vol. 2(10), pages 1-7, October.
    3. Dong, Kai & Pang, Herbert & Tong, Tiejun & Genton, Marc G., 2016. "Shrinkage-based diagonal Hotelling’s tests for high-dimensional small sample size data," Journal of Multivariate Analysis, Elsevier, vol. 143(C), pages 127-142.
    4. Shieh Albert D & Hung Yeung Sam, 2009. "Detecting Outlier Samples in Microarray Data," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 8(1), pages 1-26, February.
    5. Valkenborg Dirk & Van Sanden Suzy & Lin Dan & Kasim Adetayo & Zhu Qi & Haldermans Philippe & Jansen Ivy & Shkedy Ziv & Burzykowski Tomasz, 2008. "A Cross-Validation Study to Select a Classification Procedure for Clinical Diagnosis Based on Proteomic Mass Spectrometry," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 7(2), pages 1-22, March.
    6. Lambert-Lacroix, Sophie & Peyre, Julie, 2006. "Local likelihood regression in generalized linear single-index models with applications to microarray data," Computational Statistics & Data Analysis, Elsevier, vol. 51(3), pages 2091-2113, December.
    7. Anne-Laure Boulesteix & Robert Hable & Sabine Lauer & Manuel J. A. Eugster, 2015. "A Statistical Framework for Hypothesis Testing in Real Data Comparison Studies," The American Statistician, Taylor & Francis Journals, vol. 69(3), pages 201-212, August.
    8. Scrucca, Luca, 2007. "Class prediction and gene selection for DNA microarrays using regularized sliced inverse regression," Computational Statistics & Data Analysis, Elsevier, vol. 52(1), pages 438-451, September.
    9. Conde David & Salvador Bonifacio & Rueda Cristina & Fernández Miguel A., 2013. "Performance and estimation of the true error rate of classification rules built with additional information. An application to a cancer trial," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 12(5), pages 583-602, October.
    10. Frénay, Benoît & Doquire, Gauthier & Verleysen, Michel, 2014. "Estimating mutual information for feature selection in the presence of label noise," Computational Statistics & Data Analysis, Elsevier, vol. 71(C), pages 832-848.
    11. Kubokawa, Tatsuya & Srivastava, Muni S., 2008. "Estimation of the precision matrix of a singular Wishart distribution and its application in high-dimensional data," Journal of Multivariate Analysis, Elsevier, vol. 99(9), pages 1906-1928, October.
    12. Luca Scrucca, 2014. "Graphical tools for model-based mixture discriminant analysis," Advances in Data Analysis and Classification, Springer;German Classification Society - Gesellschaft für Klassifikation (GfKl);Japanese Classification Society (JCS);Classification and Data Analysis Group of the Italian Statistical Society (CLADAG);International Federation of Classification Societies (IFCS), vol. 8(2), pages 147-165, June.
    13. Bilin Zeng & Xuerong Meggie Wen & Lixing Zhu, 2017. "A link-free sparse group variable selection method for single-index model," Journal of Applied Statistics, Taylor & Francis Journals, vol. 44(13), pages 2388-2400, October.
    14. J. Burez & D. Van Den Poel, 2005. "CRM at a Pay-TV Company: Using Analytical Models to Reduce Customer Attrition by Targeted Marketing for Subscription Services," Working Papers of Faculty of Economics and Business Administration, Ghent University, Belgium 05/348, Ghent University, Faculty of Economics and Business Administration.
    15. Won, Joong-Ho & Lim, Johan & Yu, Donghyeon & Kim, Byung Soo & Kim, Kyunga, 2014. "Monotone false discovery rate," Statistics & Probability Letters, Elsevier, vol. 87(C), pages 86-93.
    16. Jan, Budczies & Kosztyla, Daniel & von Törne, Christian & Stenzinger, Albrecht & Darb-Esfahani, Silvia & Dietel, Manfred & Denkert, Carsten, 2014. "cancerclass: An R Package for Development and Validation of Diagnostic Tests from High-Dimensional Molecular Data," Journal of Statistical Software, Foundation for Open Access Statistics, vol. 59(i01).
    17. Jianqing Fan & Yang Feng & Jiancheng Jiang & Xin Tong, 2016. "Feature Augmentation via Nonparametrics and Selection (FANS) in High-Dimensional Classification," Journal of the American Statistical Association, Taylor & Francis Journals, vol. 111(513), pages 275-287, March.
    18. Márton Gosztonyi & Csákné Filep Judit, 2022. "Profiling (Non-)Nascent Entrepreneurs in Hungary Based on Machine Learning Approaches," Sustainability, MDPI, vol. 14(6), pages 1-20, March.
    19. Wang, Tao & Xu, Pei-Rong & Zhu, Li-Xing, 2012. "Non-convex penalized estimation in high-dimensional models with single-index structure," Journal of Multivariate Analysis, Elsevier, vol. 109(C), pages 221-235.
    20. Un Jung Lee & ShengLi Tzeng & Yu-Chuan Chen & James J Chen, 2017. "Development of Predictive Signatures for Treatment Selection in Precision Medicine," Biostatistics and Biometrics Open Access Journal, Juniper Publishers Inc., vol. 2(4), pages 83-88, August.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:eee:csdana:v:53:y:2009:i:5:p:1743-1754. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Catherine Liu (email available below). General contact details of provider: http://www.elsevier.com/locate/csda .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.