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    <responseDate>2026-10-15T07:58:19Z</responseDate>
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                <identifier>oai:data.mendeley.com/5f78c3yz6n.1</identifier>
                <datestamp>2026-09-06T21:59:02Z</datestamp>
            </header>
            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator>Gao, Biao</dc:creator>
    <dc:title>Data and code for mapping human nutrient-overload programs onto cell states across MASLD progression</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>This dataset contains the study-generated derived data, frozen analytical resources, publication source data, quality-control outputs, audit materials, and versioned R code supporting an integrative public-data study of human nutrient-overload programs across metabolic dysfunction-associated steatotic liver disease (MASLD).

The core analytical framework links four public omics resources with distinct evidentiary roles. GSE200418 was used as a direct human precision-cut liver slice perturbation anchor for deriving nutrient-response programs. GSE202379 provided donor-aware single-nucleus RNA-sequencing data for mapping these frozen programs across human MASLD cell types and cross-sectional disease states, with donors rather than nuclei or tissue specimens treated as the independent biological units. PXD051911 provided hierarchical same-study multicompartment human proteomic support. GSE312698 provided a bounded, panel-restricted, FOV/reconstructed-specimen-level descriptive spatial projection in human liver CosMx data.

The release includes ranked programs and directional gene sets, identifier harmonization resources, donor-aware cross-layer results, proteomic evidence summaries, bounded spatial-projection outputs, publication figures and tables with source data, reproducibility and quality-control records, and the retained analysis code chain.

Primary repository data are not redistributed. They should be obtained directly from NCBI GEO and ProteomeXchange/PRIDE under accession numbers GSE200418, GSE202379, GSE312698, and PXD051911. Controlled-access materials are not included.

The data support cross-dataset correspondence and orthogonal consistency analyses. They should not be interpreted as evidence of longitudinal disease progression, dietary causality, therapeutic efficacy, or an optimal intervention window.</dc:description>
    <dc:subject>Gastroenterology</dc:subject>
    <dc:subject>Genomics</dc:subject>
    <dc:subject>Proteomics</dc:subject>
    <dc:subject>Metabolism</dc:subject>
    <dc:subject>Bioinformatician</dc:subject>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/5f78c3yz6n.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/5f78c3yz6n.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
    <dc:rights>http://creativecommons.org/licenses/by/4.0</dc:rights>
    <dc:relation>https://data.mendeley.com/datasets/5f78c3yz6n</dc:relation>
    <dc:date>2026-09-06T21:59:02Z</dc:date>
</oai_dc:dc></metadata>
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