<?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>2026-06-06T17:49:30Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/7466" metadataPrefix="marc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/7466</identifier><datestamp>2026-02-03T12:03:47Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37959</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
   <leader>00925njm 22002777a 4500</leader>
   <datafield ind2=" " ind1=" " tag="042">
      <subfield code="a">dc</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Riveros, Carlos</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Ujaldon-Martínez, Manuel</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Moscato, Pablo</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2014-05-02</subfield>
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   <datafield ind2=" " ind1=" " tag="520">
      <subfield code="a">It is being increasingly accepted that traditional statistical Single &#xd;
Nucleotide Polymorphism (SNP) analysis of Genome-Wide Association &#xd;
Studies (GWAS) reveals just a small part of the heritability in complex &#xd;
diseases. Study of SNPs interactions identify additional SNPs that contribute &#xd;
to disease but that do not reach genome-wide significance or exhibit only epistatic&#xd;
effects. We have introduced a methodology for genome-wide screening &#xd;
of epistatic interactions which is feasible to be handled by state-of-art &#xd;
high performance computing technology. Unlike standard software, &#xd;
our method computes all boolean binary interactions between SNPs across &#xd;
the whole genome without assuming a particular model of interaction.&#xd;
Our extensive search for epistasis comes at the expense of higher computational&#xd;
complexity, which we tackled using graphics processors (GPUs) to reduce the&#xd;
computational time from several months in a cluster of CPUs to 3-4 days on a&#xd;
multi-GPU platform. Here, we contribute with a new&#xd;
entropy-based function to evaluate the interaction between SNPs &#xd;
which does not compromise findings about the most significant SNP &#xd;
interactions, but is more than 4000 times lighter in terms of computational time&#xd;
when running on GPUs and provides more than 100x faster code than a CPU of similar cost.&#xd;
We deploy a number of optimization techniques to tune the implementation of &#xd;
this function using CUDA and show the way to enhance scalability on larger data sets.</subfield>
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      <subfield code="a">http://hdl.handle.net/10630/7466</subfield>
   </datafield>
   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Arquitectura de ordenadores</subfield>
   </datafield>
   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Entropy-based High Performance Computation of Boolean SNP-SNP Interactions Using GPUs</subfield>
   </datafield>
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