<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-02T04:02:02Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/7263" metadataPrefix="marc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/7263</identifier><datestamp>2023-03-17T11:54:10Z</datestamp><setSpec>com_10259_3847</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_7109</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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<subfield code="a">Urda Muñoz, Daniel</subfield>
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<subfield code="a">Aragón, Francisco</subfield>
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<subfield code="a">Bautista, Rocío</subfield>
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<subfield code="a">Franco, Leonardo</subfield>
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<subfield code="a">Veredas, Francisco J.</subfield>
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<subfield code="a">Claros, Manuel Gonzalo</subfield>
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<subfield code="a">Jerez, José Manuel</subfield>
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<subfield code="a">In RNA-Seq gene expression analysis, a genetic signature or biomarker is defined as a subset of genes&#xd;
that is probably involved in a given complex human trait and usually provide predictive capabilities for that trait. The&#xd;
discovery of new genetic signatures is challenging, as it entails the analysis of complex-nature information encoded at&#xd;
gene level. Moreover, biomarkers selection becomes unstable, since high correlation among the thousands of genes&#xd;
included in each sample usually exists, thus obtaining very low overlapping rates between the genetic signatures&#xd;
proposed by different authors. In this sense, this paper proposes BLASSO, a simple and highly interpretable linear&#xd;
model with l1-regularization that incorporates prior biological knowledge to the prediction of breast cancer&#xd;
outcomes. Two different approaches to integrate biological knowledge in BLASSO, Gene-specific and Gene-disease, are&#xd;
proposed to test their predictive performance and biomarker stability on a public RNA-Seq gene expression dataset&#xd;
for breast cancer. The relevance of the genetic signature for the model is inspected by a functional analysis.</subfield>
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<subfield code="a">Trabajo presentado en: V International Work-Conference on Bioinformatics and Biomedical Engineering</subfield>
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<subfield code="a">Precision medicine</subfield>
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<subfield code="a">BLASSO: integration of biological knowledge into a regularized linear model</subfield>
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