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        <datestamp>2025-09-24T16:49:30Z</datestamp>
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              <creatorName>Petzold, Axel</creatorName>
              <givenName>Axel</givenName>
              <familyName>Petzold</familyName>
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          <titles>
            <title><![CDATA[Huntingtin Degradome Foundation Atlas]]></title>
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          <subjects>
            <subject>Proteomics and metabolomics</subject>
            <subject>Translational and applied bioinformatics</subject>
            <subject>Bioinformatics and computational biology not elsewhere classified</subject>
            <subject>Proteomics and intermolecular interactions (excl. medical proteomics)</subject>
            <subject>Computational chemistry</subject>
            <subject>Proteins and peptides</subject>
            <subject>Biological mathematics</subject>
            <subject>Huntingtin</subject>
            <subject>Huntingtin Polyglutamine-Dependent Protein Aggregation</subject>
            <subject>huntingtin interacting proteins</subject>
            <subject>Degradome</subject>
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            <date dateType="Created">2025-09-24</date>
            <date dateType="Updated">2025-09-24</date>
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          <publicationYear>2025</publicationYear>
          <publisher>University College London</publisher>
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            <description descriptionType="Abstract"><![CDATA[<h2><b>Huntingtin Degradome Foundation Atlas</b></h2><p dir="ltr">This open-access dataset introduces Version 1 of the Huntingtin Degradome Foundation Atlas, a curated proteolytic peptide resource designed to accelerate translational research in neurodegeneration.</p><p dir="ltr">The atlas integrates proteolytic fragments from Huntingtin wild-type (WT), Q75, and Q103 isoforms, capturing the impact of polyglutamine repeat expansions that drive Huntington disease (HD) pathology. By mapping and annotating these breakdown products, the dataset provides a framework for tracking disease-relevant proteolysis.</p><p dir="ltr">These data are particularly relevant for clinical researchers engaged in antisense oligonucleotide (ASO) trials or biomarker-guided therapeutic development. The atlas allows cross-referencing of peptide signatures with treatment response, supporting biomarker discovery, stratification, and outcome validation in HD studies.</p><p dir="ltr">Each peptide entry is annotated with detailed chemical features of its proteolytic origin. The dataset is delivered as a comma-delimited ASCII (.csv) file for integration into bioinformatics and statistical pipelines. For efficient distribution, it is provided in compressed format, which can be extracted using:</p><h4>tar -xvJf Huntingtin_WT_Degradome_Foundation_Atlas_v1.tar.gz<br></h4><p dir="ltr"><b>Reproducibility</b><br>All datasets can be regenerated using open-source tools (Python, BLAST, SAS). Fully documented Python scripts are included in the repository to ensure transparency and adaptability to local environments, following the methodology described in [1].</p><p dir="ltr"><br></p><p dir="ltr"><b>Reference</b><br>[1] Petzold A. <i>Proteolysis-Based Biomarker Repertoire of the Neurofilament Proteome.</i> J Neurochem. 2025 Mar;169(3):e70023. doi: 10.1111/jnc.70023. PMID: 40066701; PMCID: PMC11894590.</p><p><br></p>]]></description>
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