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Variational Autoencoders for Cancer Data Integration: Design Principles and Computational Practice

Authors :
Helena Andrés-Terré
Ifrah Tariq
Nikola Simidjievski
Paul Scherer
Cristian Bodnar
Zohreh Shams
Pietro Liò
Mateja Jamnik
Simidjievski, Nikola [0000-0003-3948-6370]
Scherer, Paul [0000-0002-2240-7501]
Andres Terre, Helena [0000-0001-7199-7897]
Shams, Zohreh [0000-0002-0143-798X]
Jamnik, Mateja [0000-0003-2772-2532]
Lio, Pietro [0000-0002-0540-5053]
Apollo - University of Cambridge Repository
Source :
Frontiers in Genetics, Frontiers in Genetics, Vol 10 (2019)
Publication Year :
2020
Publisher :
Apollo - University of Cambridge Repository, 2020.

Abstract

International initiatives such as the Molecular Taxonomy of Breast Cancer International Consortium (METABRIC), Cancer Genome Atlas (TCGA), and the International Cancer Genome Consortium (ICGC) are collecting multiple data sets at different genome-scales with the aim to identify novel cancer bio-markers and predict patient survival. To analyse such data, several machine learning, bioinformatics and statistical methods have been applied, among them neural networks such as autoencoders. Although these models provide a good statistical learning framework to analyse multi-omic and/or clinical data, there is a distinct lack of work on how to integrate diverse patient data and identify the optimal design best suited to the available data. In this paper, we investigate several autoencoder architectures that integrate a variety of cancer patient data types (e.g., multi-omics and clinical data). We perform extensive analyses of these approaches and provide a clear methodological and computational framework for designing systems that enable clinicians to investigate cancer traits and translate the results into clinical applications. We demonstrate how these networks can be designed, built and, in particular, applied to tasks of integrative analyses of heterogeneous breast cancer data. The results show that these approaches yield relevant data representations that, in turn, lead to accurate and stable diagnosis.

Details

Database :
OpenAIRE
Journal :
Frontiers in Genetics, Frontiers in Genetics, Vol 10 (2019)
Accession number :
edsair.doi.dedup.....4efaff7dc429152345e263147898b900
Full Text :
https://doi.org/10.17863/cam.49045