IDEAS home Printed from https://ideas.repec.org/a/eee/csdana/v55y2011i1p903-913.html
   My bibliography  Save this article

Floating prioritized subset analysis: A powerful method to detect differentially expressed genes

Author

Listed:
  • Lin, Wan-Yu
  • Lee, Wen-Chung

Abstract

Controlling the false discovery rate (FDR) is a powerful approach to deal with a large number of hypothesis tests, such as in gene expression data analyses and genome-wide association studies. To further boost power, here we propose a floating prioritized subset analysis (floating PSA) that can more effectively use prior knowledge and detect more genes that are differentially expressed. Genes are first allocated into two subsets: a prioritized subset and a non-prioritized subset, according to investigators' prior biological knowledge. We allow the FDRs of the two subsets to vary freely (to float) but aim to control the overall FDR at a desired level. An algorithm for the floating PSA is developed to detect the largest number of true positives. Theoretical justifications of the algorithm are given, and computer simulation studies show that the method has good statistical properties. We apply this method to detect genes that are differentially expressed between acute lymphoblastic leukemia and acute myeloid leukemia patients. The result shows that our floating PSA identifies 32 more genes (permutation-based FDR=0.0427) than the conventional (fixed) FDR control. Another example is a colon cancer study, and our floating PSA identifies 43 more genes (permutation-based FDR=0.0502). The floating PSA method is to be recommended for the detection of differentially expressed genes, in light of its power, robustness, and ease of implementation.

Suggested Citation

  • Lin, Wan-Yu & Lee, Wen-Chung, 2011. "Floating prioritized subset analysis: A powerful method to detect differentially expressed genes," Computational Statistics & Data Analysis, Elsevier, vol. 55(1), pages 903-913, January.
  • Handle: RePEc:eee:csdana:v:55:y:2011:i:1:p:903-913
    as

    Download full text from publisher

    File URL: http://www.sciencedirect.com/science/article/pii/S0167-9473(10)00310-5
    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. Cheng Cheng & Pounds Stanley B. & Boyett James M. & Pei Deqing & Kuo Mei-Ling & Roussel Martine F., 2004. "Statistical Significance Threshold Criteria For Analysis of Microarray Gene Expression Data," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 3(1), pages 1-32, December.
    2. Alice Whittemore, 2007. "A Bayesian False Discovery Rate for Multiple Testing," Journal of Applied Statistics, Taylor & Francis Journals, vol. 34(1), pages 1-9.
    3. Christopher R. Genovese & Kathryn Roeder & Larry Wasserman, 2006. "False discovery control with p-value weighting," Biometrika, Biometrika Trust, vol. 93(3), pages 509-524, September.
    4. John D. Storey, 2002. "A direct approach to false discovery rates," Journal of the Royal Statistical Society Series B, Royal Statistical Society, vol. 64(3), pages 479-498, August.
    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. Xiaoquan Wen, 2017. "Robust Bayesian FDR Control Using Bayes Factors, with Applications to Multi-tissue eQTL Discovery," Statistics in Biosciences, Springer;International Chinese Statistical Association, vol. 9(1), pages 28-49, June.
    2. Cheng, Cheng, 2009. "Internal validation inferences of significant genomic features in genome-wide screening," Computational Statistics & Data Analysis, Elsevier, vol. 53(3), pages 788-800, January.
    3. Ang Li & Rina Foygel Barber, 2017. "Accumulation Tests for FDR Control in Ordered Hypothesis Testing," Journal of the American Statistical Association, Taylor & Francis Journals, vol. 112(518), pages 837-849, April.
    4. Yoav Benjamini, 2010. "Discovering the false discovery rate," Journal of the Royal Statistical Society Series B, Royal Statistical Society, vol. 72(4), pages 405-416, September.
    5. Hunt, Daniel L. & Cheng, Cheng & Pounds, Stanley, 2009. "The beta-binomial distribution for estimating the number of false rejections in microarray gene expression studies," Computational Statistics & Data Analysis, Elsevier, vol. 53(5), pages 1688-1700, March.
    6. Andrew Y. Chen, 2022. "Most claimed statistical findings in cross-sectional return predictability are likely true," Papers 2206.15365, arXiv.org, revised Sep 2024.
    7. Zhao, Haibing & Fung, Wing Kam, 2016. "A powerful FDR control procedure for multiple hypotheses," Computational Statistics & Data Analysis, Elsevier, vol. 98(C), pages 60-70.
    8. Zhao, Haibing, 2014. "Adaptive FWER control procedure for grouped hypotheses," Statistics & Probability Letters, Elsevier, vol. 95(C), pages 63-70.
    9. Haibing Zhao & Wing Kam Fung, 2018. "Controlling mixed directional false discovery rate in multidimensional decisions with applications to microarray studies," TEST: An Official Journal of the Spanish Society of Statistics and Operations Research, Springer;Sociedad de Estadística e Investigación Operativa, vol. 27(2), pages 316-337, June.
    10. Wenguang Sun & T. Tony Cai, 2009. "Large‐scale multiple testing under dependence," Journal of the Royal Statistical Society Series B, Royal Statistical Society, vol. 71(2), pages 393-424, April.
    11. Bickel David R., 2013. "Simple estimators of false discovery rates given as few as one or two p-values without strong parametric assumptions," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 12(4), pages 529-543, August.
    12. Otília Menyhart & Boglárka Weltz & Balázs Győrffy, 2021. "MultipleTesting.com: A tool for life science researchers for multiple hypothesis testing correction," PLOS ONE, Public Library of Science, vol. 16(6), pages 1-12, June.
    13. Habiger, Joshua D. & Peña, Edsel A., 2014. "Compound p-value statistics for multiple testing procedures," Journal of Multivariate Analysis, Elsevier, vol. 126(C), pages 153-166.
    14. Youngchao Ge & Sandrine Dudoit & Terence Speed, 2003. "Resampling-based multiple testing for microarray data analysis," TEST: An Official Journal of the Spanish Society of Statistics and Operations Research, Springer;Sociedad de Estadística e Investigación Operativa, vol. 12(1), pages 1-77, June.
    15. Bajgrowicz, Pierre & Scaillet, Olivier, 2012. "Technical trading revisited: False discoveries, persistence tests, and transaction costs," Journal of Financial Economics, Elsevier, vol. 106(3), pages 473-491.
    16. Wen Shi & Xi Chen & Jennifer Shang, 2019. "An Efficient Morris Method-Based Framework for Simulation Factor Screening," INFORMS Journal on Computing, INFORMS, vol. 31(4), pages 745-770, October.
    17. Dørum Guro & Snipen Lars & Solheim Margrete & Saebo Solve, 2011. "Smoothing Gene Expression Data with Network Information Improves Consistency of Regulated Genes," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 10(1), pages 1-26, August.
    18. Jianqing Fan & Xu Han, 2017. "Estimation of the false discovery proportion with unknown dependence," Journal of the Royal Statistical Society Series B, Royal Statistical Society, vol. 79(4), pages 1143-1164, September.
    19. A Bottle & P Aylin, 2011. "Predicting the false alarm rate in multi-institution mortality monitoring," Journal of the Operational Research Society, Palgrave Macmillan;The OR Society, vol. 62(9), pages 1711-1718, September.
    20. Van Hanh Nguyen & Catherine Matias, 2014. "On Efficient Estimators of the Proportion of True Null Hypotheses in a Multiple Testing Setup," Scandinavian Journal of Statistics, Danish Society for Theoretical Statistics;Finnish Statistical Society;Norwegian Statistical Association;Swedish Statistical Association, vol. 41(4), pages 1167-1194, December.

    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:55:y:2011:i:1:p:903-913. 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.