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                <identifier>oai:data.mendeley.com/68k3bsz2tz.1</identifier>
                <datestamp>2025-10-10T14:01:13Z</datestamp>
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            <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>Cui, Zekai</dc:creator>
    <dc:title>Single-Cell Transcriptomics of Nfe2l2-KO versus WT Mouse Corneas</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Fresh corneas from WT and Nfe2l2-KO mice at P14/P28 (n = 5/group, 4-month-old) were dissociated with papain (20 U/mL) + DNase I for 15–20 min at 37 °C, quenched with ovomucoid, filtered (40 µm), and processed on a droplet-based scRNA-seq platform. Library preparation and sequencing were outsourced to Singleron Biotechnologies (Nanjing, China). Raw reads were aligned to mm10 with STAR/Drop-seq Tools; ambient RNA was corrected with SoupX. In Seurat v5, low/high feature outliers and high-mitochondrial cells were removed, doublets were filtered (DoubletFinder), SCTransform normalization and integration were applied, clusters were identified by SNN/UMAP, and annotated with canonical markers. Differential expression used Wilcoxon with BH FDR &lt; 0.05. Functional enrichment of DEGs was performed with Metascape. Cell–cell communication was inferred with CellChat v1.6 (MouseDB; 1,000 permutations; FDR &lt; 0.05) and summarized at pathway level.</dc:description>
    <dc:subject>Cornea</dc:subject>
    <dc:subject>Keratoconus</dc:subject>
    <dc:subject>Single-Cell RNA Sequencing</dc:subject>
    <dc:subject>Transcription Factor Nrf2</dc:subject>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/68k3bsz2tz.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/68k3bsz2tz.1</dc:identifier>
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    <dc:date>2025-10-10T14:01:13Z</dc:date>
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