Abstract
Golub et al. started their research to find oncogenes and new cancer subclasses from microarray around 1970. They opened their microarray on the Internet. The other five medical projects published their papers and released their microarrays, also. However, because Japanese cancer specialist advised us that NIH decided that these researches were useless after 2004, we guess medical groups abandoned these researches. Although we are looking for NIH’s report, we cannot find it now. Meanwhile, many researchers of statistics, machine learning and bioengineering continue to research as a new theme of high-dimensional data analysis using microarrays. However, they could not succeed in cancer gene analysis as same as medical researches (Problem5). We discriminated six microarrays by Revised IP-OLDF (RIP) and solved Problem5 within 54 days until December 20, 2015. We obtained the two surprising results. First, MNMs of six microarrays are zero (Fact3). Second, RIP could decompose microarray into many linearly separable gene subspaces (SMs) and noise subspace (Fact4). These two new facts indicate that we are free from the curse of high dimensional microarray data and complete the cancer gene analysis. Because all SMs are LSD and small samples, we thought to analysis all SMs by statistical methods and obtained useful results. However, we were disappointed that statistical methods do not show linearly separable facts and are useless for cancer gene diagnosis (Problem6). After trial and error, we make signal data made by RIP discriminant scores (RipDSs) from SM. Through this breakthrough, we find useful information by correlation analysis, cluster analysis, and PCA in addition to RIP, Revised LP-OLDF and hard margin SVM (H-SVM). We think that the discovery of the above two new facts is the essence of Problem5. Moreover, we claim to solve Prpblem6 and obtain useful medical care information from signal data as a cancer gene diagnosis. However, our claim needs validation by medical specialists. In this research, we introduce the reason why no researchers could succeed in the cancer gene diagnosis by microarrays from 1970.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Alon, U., et al.: Broad patterns of gene expression revealed by clustering analysis of cancer and normal colon tissues probed by oligonucleotide arrays. Proc. Natl. Acad. Sci. USA 96, 6745–6750 (1999)
Aoshima, M., Yata, K.: Distance-based classifier by data transformation for high-dimension, strongly spiked eigenvalue models. Ann. Inst. Stat. Math. 71, 473–503 (2019)
Aoshima, M., Yata, K.: High-dimensional quadratic classifiers in non-sparse settings. Methodol. Comput. Appl. Probabil. (in press, 2019)
Brahim, A.B., Lima, M: Hybrid instance based feature selection algorithms for cancer diagnosis. Pattern Recognition Letters, pp. 8. 2014
Buhlmann, P., Geer, A.B.: Statistics for high-dimensional data-method, theory, and applications. Springer, Berlin (2011)
Charikar, M., Guruswami, V., Kumar, R., Rajagopalan, S., Sahai, A.: Combinatorial feature selection problems. IEEE Xplore, pp. 631–640 (2000)
Chiaretti, S. et al.: Gene Expression Profile of Adult T-cell Acute Lymphocytic Leukemia Identifies Distinct Subsets of Patients with Different Response to Therapy And Survival. Blood. April 1, 2004, 103/7, pp. 2771–2778 (2004)
Cilia, N.D., Claudio, D.S., Francesco, F., Stefano, R., Alessandra, S.F.: An experimental comparison of feature-selection and classification methods for microarray datasets. Information 10(109), 1–13 (2019)
Cox, D.R.: The regression analysis of binary sequences (with discussion). J. Roy Stat. Soc. B 20 215–242 (1958)
Diao, G., Vidyashankar, A.N.: Assessing genome-wide statistical significance for large p small n problems. Genetics 194, 781–783 (2013)
Firth, D.: “Bias reduction of maximum likelihood estimates. Biometrika 80, 27–39 (1993)
Fisher, R.A.: Statistical Methods and Statistical Inference. Hafner Publishing Co., New Zealand (1956)
Flury, B., Riedwyl, H.: Multivariate Statistics: A Practical Approach. Cambridge University Press, New York (1988)
Friedman, J.H.: Regularized discriminant analysis. J. Am. Stat. Assoc. 84(405), 165–175 (1989)
Golub, T.R. et al.: Molecular classification of cancer: class discovery and class prediction by gene expression monitoring. Science. 1999 Oct 15, 286/5439, 531–537 (1999)
Goodnight, J.H.: SAS Technical Report – The Sweep Operator: Its Importance in Statistical Computing – R (100). SAS Institute Inc. USA (1978)
Jeffery, I.B., Higgins, D.G., Culhane, C: Comparison and evaluation of methods for generating differentially expressed gene lists from microarray data. BMC Bioinformat. (2006)
Lachenbruch, P.A., Mickey, M.R.: Estimation of error rates in discriminant analysis. Technometrics 10(1), 11 (1968)
Miyake, A., Shinmura, S.: Error rate of linear discriminant function. In: Dombal, F.T., Gremy, F. (ed.) North-Holland Publishing Company. The Netherland, pp. 435–445 (1976)
Miyake, A., Shinmura, S.: An algorithm for the optimal linear discriminant function and its application. Jpn Soc. Med. Electron Bio. Eng. 1815, 452–454 (1980)
Sall, J.P., Creighton, L., Lehman, A.: JMP Start Statistics, Third Edition. SAS Institute Inc. 2004. (S. Shinmura, Supervise Japanese Version)
Schrage, L.: Optimization Modeling with LINGO. LINDO Systems Inc. (2006)
Shinmura, S.: Optimal Linear Discriminant Functions Using Mathematical Programming. Dissertation, Okayama University, Japan, pp. 1–101 (2000)
Shinmura, S.: A new algorithm of the linear discriminant function using integer programming. New Trends Probab. Stat. 5, 133–142 (2000)
S. Shinmura, The optimal linear discriminant function, Union of Japanese Scientist and Engineer Publishing, Japan (ISBN 978-4-8171-9364-3), 2010
Shinmura, S.: Problem of discriminant analysis by mark sense test data. Japanese Soc. Appl. Stat. 4012, 157–172 (2011)
Shinmura, S.: End of Discriminant Functions based on Variance-Covariance Matrices. ICORES, pp. 5–16 (2014)
Shinmura, S.: Four Serious Problems and New Facts of the Discriminant Analysis. In: Pinson, E., et al. (eds.) Operations Research and Enterprise Systems, pp. 15–30. Springer, Berlin (2015)
Shinmura, S.: New Theory of Discriminant Analysis after R. Springer, Fisher (2016)
Shinmura, S.: Cancer Gene Analysis to Cancer Gene Diagnosis, Amazon (2017)
Shinmura, S.: Cancer Gene Analysis by Singh et al. Microarray Data. ISI2017, pp. 1–6 (2017)
Shinmura, S.: Cancer Gene Analysis of Microarray Data. BCD18, pp. 1–6 (2018)
Shinmura, S.: First Success of Cancer Gene Analysis by Microarrays, pp. 1–7. Biocomp’18 (2018)
Shinmura, S.: High-Dimensional Microarray Data Analysis. Springer (2019)
Shinmura, S.: High-dimensional microarray data analysis—first success of cancer gene analysis and cancer gene diagnosis. August ISI2019, in Press (2019)
Shipp, M.A., et al.: Diffuse large B-cell lymphoma outcome prediction by gene-expression profiling and supervised machine learning. Nat. Med. 8, 68–74 (2002)
Singh, D., et al.: Gene expression correlates of clinical prostate cancer behavior. Cancer Cell, 1, 203–209
Stam, A.: Non-traditional approaches to statistical classifications: some perspectives on Lp-norm methods. Ann. Oper. Res. 74, 1–36 (1997)
Tian, E., et al.: The role of the Wnt-signaling antagonist DKK1 in the development of osteolytic lesions in multiple myeloma. New Eng. J. Med. 349(26), 2483–2494 (2003)
Vapnik, V.: The Nature of Statistical Learning Theory.Springer. 1999
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2020 Springer Nature Switzerland AG
About this chapter
Cite this chapter
Shinmura, S. (2020). Release from the Curse of High Dimensional Data Analysis. In: Lee, R. (eds) Big Data, Cloud Computing, and Data Science Engineering. BCD 2019. Studies in Computational Intelligence, vol 844. Springer, Cham. https://doi.org/10.1007/978-3-030-24405-7_12
Download citation
DOI: https://doi.org/10.1007/978-3-030-24405-7_12
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-24404-0
Online ISBN: 978-3-030-24405-7
eBook Packages: Intelligent Technologies and RoboticsIntelligent Technologies and Robotics (R0)