Unsupervised Feature Selection for Tumor Profiles using Autoencoders and
Kernel Methods
- URL: http://arxiv.org/abs/2007.06106v1
- Date: Sun, 12 Jul 2020 21:59:05 GMT
- Title: Unsupervised Feature Selection for Tumor Profiles using Autoencoders and
Kernel Methods
- Authors: Martin Palazzo, Pierre Beauseroy, Patricio Yankilevich
- Abstract summary: This work aims to learn meaningful and low dimensional representations of tumor samples and find tumor subtype clusters.
The proposed method named Latent Kernel Feature Selection (LKFS) is an unsupervised approach for gene selection in tumor gene expression profiles.
- Score: 1.9078991171384014
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: Molecular data from tumor profiles is high dimensional. Tumor profiles can be
characterized by tens of thousands of gene expression features. Due to the size
of the gene expression feature set machine learning methods are exposed to
noisy variables and complexity. Tumor types present heterogeneity and can be
subdivided in tumor subtypes. In many cases tumor data does not include tumor
subtype labeling thus unsupervised learning methods are necessary for tumor
subtype discovery. This work aims to learn meaningful and low dimensional
representations of tumor samples and find tumor subtype clusters while keeping
biological signatures without using tumor labels. The proposed method named
Latent Kernel Feature Selection (LKFS) is an unsupervised approach for gene
selection in tumor gene expression profiles. By using Autoencoders a low
dimensional and denoised latent space is learned as a target representation to
guide a Multiple Kernel Learning model that selects a subset of genes. By using
the selected genes a clustering method is used to group samples. In order to
evaluate the performance of the proposed unsupervised feature selection method
the obtained features and clusters are analyzed by clinical significance. The
proposed method has been applied on three tumor datasets which are Brain, Renal
and Lung, each one composed by two tumor subtypes. When compared with benchmark
unsupervised feature selection methods the results obtained by the proposed
method reveal lower redundancy in the selected features and a better clustering
performance.
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