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                  <mods:namePart>López-García, Guillermo</mods:namePart>
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                  <mods:namePart>Jerez-Aragonés, José Manuel</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Franco, Leonardo</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Veredas-Navarro, Francisco Javier</mods:namePart>
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               <mods:identifier type="uri">https://hdl.handle.net/10630/17831</mods:identifier>
               <mods:abstract>The diagnosis and prognosis of cancer are among the more&#xd;
challenging tasks that oncology medicine deals with. With the main aim&#xd;
of fitting the more appropriate treatments, current personalized medicine&#xd;
focuses on using data from heterogeneous sources to estimate the evolu-&#xd;
tion of a given disease for the particular case of a certain patient. In recent&#xd;
years, next-generation sequencing data have boosted cancer prediction by&#xd;
supplying gene-expression information that has allowed diverse machine&#xd;
learning algorithms to supply valuable solutions to the problem of cancer&#xd;
subtype classification, which has surely contributed to better estimation&#xd;
of patient’s response to diverse treatments. However, the efficacy of these&#xd;
models is seriously affected by the existing imbalance between the high&#xd;
dimensionality of the gene expression feature sets and the number of sam-&#xd;
ples available for a particular cancer type. To counteract what is known&#xd;
as the curse of dimensionality, feature selection and extraction methods&#xd;
have been traditionally applied to reduce the number of input variables&#xd;
present in gene expression datasets. Although these techniques work by&#xd;
scaling down the input feature space, the prediction performance of tradi-&#xd;
tional machine learning pipelines using these feature reduction strategies&#xd;
remains moderate. In this work, we propose the use of the Pan-Cancer&#xd;
dataset to pre-train deep autoencoder architectures on a subset com-&#xd;
posed of thousands of gene expression samples of very diverse tumor&#xd;
types. The resulting architectures are subsequently fine-tuned on a col-&#xd;
lection of specific breast cancer samples. This transfer-learning approach&#xd;
aims at combining supervised and unsupervised deep learning models&#xd;
with traditional machine learning classification algorithms to tackle the&#xd;
problem of breast tumor intrinsic-subtype classification.</mods:abstract>
               <mods:language>
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               <mods:subject>
                  <mods:topic>Cáncer - Diagnóstico</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Computación, Teoría de la</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Congresos y conferencias</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>A transfer-learning approach to feature extraction from cancer transcriptomes with deep autoencoders</mods:title>
               </mods:titleInfo>
               <mods:genre>conference output</mods:genre>
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