<?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>2026-06-02T00:41:33Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/27339" metadataPrefix="marc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/27339</identifier><datestamp>2026-02-03T12:07:54Z</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">
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      <subfield code="a">Pérez-Tejeiro, José Miguel</subfield>
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      <subfield code="a">Csukasi, Fabiana</subfield>
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      <subfield code="a">Becerra-Ratia, José</subfield>
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      <subfield code="a">Durán-Jimenez, Iván Jesús</subfield>
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      <subfield code="a">Fernández-Pozo, Noé</subfield>
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      <subfield code="c">2023</subfield>
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      <subfield code="a">Gene expression atlases are powerful bioinformatics tools that&#xd;
allow access to the scientific community to explore omics data. In&#xd;
biomedicine, numerous gene expression databases are available, yet&#xd;
none provide enough information about localized transcriptomics in the&#xd;
skeletal system. In this work we try to solve this gap of knowledge by&#xd;
creating a transcriptomic atlas which brings together different works&#xd;
across the skeletal system, analyzing several key tissue compartments&#xd;
in normal and pathological conditions from mouse and human after&#xd;
analyzing more than 200 studies. Our atlas shows a user-friendly&#xd;
representation which allows the comparison of multiple genes across&#xd;
the different tissues of the skeleton: bone, cartilage, tendon, ligament,&#xd;
growth plate and skeletal muscle. As expected, our first finding was&#xd;
the identification of a significant heterogeneity between experiments&#xd;
from similar studies but from different labs, so we have created a&#xd;
dataset processing pipeline with inclusive/exclusive criteria of RNAseq&#xd;
experiments based in sequencing quality and purity of the analyzed&#xd;
tissues in search of a normalization protocol. We believe that this atlas&#xd;
will allow the homogenization of the public transcriptomic studies in the&#xd;
skeleton and will settle the basis to incorporate the upcoming data from&#xd;
single cell transcriptomics studies.</subfield>
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      <subfield code="a">https://hdl.handle.net/10630/27339</subfield>
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      <subfield code="a">Genómica funcional</subfield>
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      <subfield code="a">Bioinformática</subfield>
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      <subfield code="a">The Skeletal Atlas: A holistic approach to transcriptomics in the skeleton.</subfield>
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