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Updated: May 25, 2026

Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances
Published on: October 11, 2018
A novel significance score for gene selection and ranking
Yufei Xiao1, Tzu-Hung Hsiao, Uthra Suresh
1Department of Epidemiology and Biostatistics, Computational Biology and Bioinformatics Division, Greehey Children's Cancer Research Institute, Department of Surgery, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, United States Army Institute of Surgical Research, Fort Sam Houston, TX 78234 and Cancer Therapy and Research Center, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Motivation:
When identifying differentially expressed (DE) genes from high-throughput gene expression measurements, we would like to take both statistical significance (such as P-value) and biological relevance (such as fold change) into consideration. In gene set enrichment analysis (GSEA), a score that can combine fold change and P-value together is needed for better gene ranking.
Results:
We defined a gene significance score π-value by combining expression fold change and statistical significance (P-value), and explored its statistical properties. When compared to various existing methods, π-value based approach is more robust in selecting DE genes, with the largest area under curve in its receiver operating characteristic curve. We applied π-value to GSEA and found it comparable to P-value and t-statistic based methods, with added protection against false discovery in certain situations. Finally, in a gene functional study of breast cancer profiles, we showed that using π-value helps elucidating otherwise overlooked important biological functions.
Availability:
http://gccri.uthscsa.edu/Pi_Value_Supplementary.asp
Contact:
xy@ieee.org, cheny8@uthscsa.edu
Supplementary Information:
Supplementary data are available at Bioinformatics online.
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