AFExNet

AFExNet leverages adversarial autoencoders (AAE) to differentiate breast cancer sub-types and extract biologically relevant genes from high-dimensional RNA-Seq data.


Key Features:

  • Adversarial Autoencoder Architecture: Employs a dual-stage AAE architecture combining unsupervised pre-training with supervised fine-tuning to learn latent representations from high-dimensional genomic data.
  • Classifier Independence: Demonstrated robust performance when evaluated using twelve different supervised classifiers on public RNA-Seq datasets of breast cancer.
  • Feature Extraction Capability: Extracts meaningful latent features from genetic data that support characterization of breast cancer sub-types.
  • TopGene Method: Identifies highly weighted genes from the model latent space as candidate biomarkers for downstream analysis.

Scientific Applications:

  • Breast Cancer Sub-type Classification: Differentiates breast cancer sub-types using RNA-Seq–derived latent representations.
  • Biomarker Discovery: Identifies highly weighted genes from the latent space that serve as potential diagnostic or therapeutic biomarkers.
  • Mechanistic Characterization: Provides molecular feature sets that can inform studies of disease mechanisms and heterogeneity in oncology.
  • Translational Research Framework: Offers a framework applicable to other complex diseases with genetic heterogeneity for feature extraction from high-throughput genomic data.

Methodology:

Two-stage approach comprising unsupervised pre-training with an adversarial autoencoder to learn a latent representation, followed by supervised fine-tuning using labeled data.

Topics

Details

License:
CC-BY-4.0
Tool Type:
command-line tool
Programming Languages:
Python
Added:
6/14/2021
Last Updated:
8/9/2021

Operations

Publications

Mondol RK, Truong ND, Reza M, Ippolito S, Ebrahimie E, Kavehei O. AFExNet: An Adversarial Autoencoder for Differentiating Breast Cancer Sub-Types and Extracting Biologically Relevant Genes. IEEE/ACM Transactions on Computational Biology and Bioinformatics. 2022;19(4):2060-2070. doi:10.1109/tcbb.2021.3066086. PMID:33720833.