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Abstract Motivation Detecting cancer gene expression and transcriptome changes with mRNA-sequencing (RNA-Seq) or array-based data are important for understanding the molecular mechanisms underlying carcinogenesis and cellular events during cancer progression. In previous studies, the differentially expressed genes were detected across patients in one cancer type. These studies ignored the role of mRNA expression changes in driving tumorigenic mechanisms that are either universal or specific in different tumor types. To address the problem, we introduce two network-based multi-task learning frameworks, NetML and NetSML, to discover common differentially expressed genes shared across different cancer types as well as differentially expressed genes specific to each cancer type. The proposed frameworks consider the common latent gene co-expression modules and gene-sample biclusters underlying the multiple cancer datasets to learn the knowledge crossing different tumor types. Results Large-scale experiments on simulations and real cancer high-throughput datasets validate that the proposed network-based multi-task learning frameworks perform better sample classification compared with the models without the knowledge sharing across different cancer types. The common and cancer specific molecular signatures detected by multi-task learning frameworks on TCGA ovarian cancer, breast cancer, and prostate cancer datasets are correlated with the known marker genes and enriched in cancer relevant KEGG pathways and Gene Ontology terms. Availability and Implementation Source code is available at: https://github.com/compbiolabucf/NetML Supplementary information Supplementary data are available at Bioinformatics
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This content will become publicly available on January 24, 2026
Normalization and selecting non-differentially expressed genes improve machine learning modelling of cross-platform transcriptomic data
Normalization is a critical step in quantitative analyses of biological processes. Recent works show that cross-platform integration and normalization enable machine learning (ML) training on RNA microarray and RNA-seq data, but no independent datasets were used in their studies. Therefore, it is unclear how to improve ML modelling performance on independent RNA array and RNA-seq based datasets. Inspired by the house-keeping genes that are commonly used in experimental biology, this study tests the hypothesis that non-differentially expressed genes (NDEG) may improve normalization of transcriptomic data and subsequently cross-platform modelling performance of ML models. Microarray and RNA-seq datasets of the TCGA breast cancer were used as independent training and test datasets, respectively, to classify the molecular subtypes of breast cancer. NDEG (p>0.85) and differentially expressed genes (DEG, p<0.05) were selected based on the p values of ANOVA analysis and used for subsequent data normalization and classification, respectively. Models trained based on data from one platform were used for testing on the other platform. Our data show that NDEG and DEG gene selection could effectively improve the model classification performance. Normalization methods based on parametric statistical analysis were inferior to those based on nonparametric statistics. In this study, the LOG_QN and LOG_QNZ normalization methods combined with the neural network classification model seem to achieve better performance. Therefore, NDEG-based normalization appears useful for cross-platform testing on completely independent datasets. However, more studies are required to examine whether NDEG-based normalization can improve ML classification performance in other datasets and other omic data types.
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- Award ID(s):
- 2128307
- PAR ID:
- 10568348
- Publisher / Repository:
- arxiv.org
- Date Published:
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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