<?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>2026-04-29T02:37:31Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/26553" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/26553</identifier><datestamp>2025-12-18T13:01:17Z</datestamp><setSpec>com_20.500.12105_2052</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19609</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">
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      <subfield code="a">Boeckaerts, Dimitri</subfield>
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      <subfield code="a">Stock, Michiel</subfield>
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      <subfield code="a">Ferriol-González, Celia</subfield>
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      <subfield code="a">Oteo-Iglesias, Jesus</subfield>
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      <subfield code="a">Sanjuán, Rafael</subfield>
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      <subfield code="a">Domingo-Calap, Pilar</subfield>
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      <subfield code="a">De Baets, Bernard</subfield>
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      <subfield code="a">Briers, Yves</subfield>
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      <subfield code="c">2024-05-22</subfield>
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      <subfield code="a">Phages are increasingly considered promising alternatives to target drug-resistant bacterial pathogens. However, their often-narrow host range can make it challenging to find matching phages against bacteria of interest. Current computational tools do not accurately predict interactions at the strain level in a way that is relevant and properly evaluated for practical use. We present PhageHostLearn, a machine learning system that predicts strain-level interactions between receptor-binding proteins and bacterial receptors for Klebsiella phage-bacteria pairs. We evaluate this system both in silico and in the laboratory, in the clinically relevant setting of finding matching phages against bacterial strains. PhageHostLearn reaches a cross-validated ROC AUC of up to 81.8% in silico and maintains this performance in laboratory validation. Our approach provides a framework for developing and evaluating phage-host prediction methods that are useful in practice, which we believe to be a meaningful contribution to the machine-learning-guided development of phage therapeutics and diagnostics.</subfield>
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      <subfield code="a">Boeckaerts D, Stock M, Ferriol-González C, Oteo-Iglesias J, Sanjuán R, Domingo-Calap P, De Baets B, Briers Y. Prediction of Klebsiella phage-host specificity at the strain level. Nat Commun. 2024 May 22;15(1):4355.</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.12105/26553</subfield>
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      <subfield code="a">38778023</subfield>
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      <subfield code="a">10.1038/s41467-024-48675-6</subfield>
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      <subfield code="a">2041-1723</subfield>
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      <subfield code="a">Nature communications</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Prediction of Klebsiella phage-host specificity at the strain level</subfield>
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