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Omics · dataset · 2025

Single-Cell Transcriptomics of Nfe2l2-KO versus WT Mouse Corneas

Listed in Teesside University Research Data Repository

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.

Description

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 < 0.05. Functional enrichment of DEGs was performed with Metascape.

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Cell–cell communication was inferred with CellChat v1.6 (MouseDB; 1,000 permutations; FDR < 0.05) and summarized at pathway level.

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Where it is published

Catalogue records · 1

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Inferred from text
Sequencing 75%
Provenance · 1 source records, 12 field assertions
SourceKeyLast seenRaw
Teesside University Research Data Repositoryoai:data.mendeley.com/68k3bsz2tz.19 d agoJSON v1
FieldAssertionExtractorEvidence
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concepts[modality].local:modality:single-cell-rna-seqmapping · researchdata tees ac ukvocabulary-mapper@1.0.0keywords['Single-Cell RNA Sequencing']
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