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Human Optic Nerve Endothelial Cells (snRNA-seq) Dataset
Dataset Overview
This dataset comprises single-nucleus RNA sequencing (snRNA-seq) data specifically focusing on endothelial cells from the human optic nerve and optic nerve head. It represents a valuable resource for investigating cell-type specific gene expression profiles within a critical ocular tissue.
The data was sourced from the CZ CELLxGENE Discover API, providing access to a deeply characterized single-cell atlas. It has been processed and converted into standardized .h5ad
and .parquet
formats for ease of use in machine learning and bioinformatics pipelines, enabling high-resolution insights into tissue biology.
Relevance to Aging Research
The human optic nerve and optic nerve head are highly susceptible to age-related degeneration, playing a critical role in conditions like glaucoma, a leading cause of irreversible blindness, which is strongly associated with aging. Endothelial cells, forming the lining of blood vessels, are crucial for maintaining tissue homeostasis, nutrient supply, and waste removal in the optic nerve.
Age-related changes in endothelial cell function, integrity, and gene expression are known to contribute to vascular dysfunction, inflammation, and cellular senescence, all of which are hallmarks of aging. By providing a single-cell resolution view of these specific cells, this dataset offers an unprecedented opportunity to:
- Identify age-specific molecular signatures within optic nerve endothelial cells.
- Uncover how cellular processes like metabolism, inflammation, and stress response change with age at the single-cell level.
- Discover biomarkers or therapeutic targets related to age-associated optic neuropathies.
- Investigate the contribution of endothelial cell aging to the overall aging process of the visual system.
This dataset thus serves as a powerful resource for understanding the intricate molecular mechanisms of aging within a vital human tissue.
Data Details
- Organism: Homo sapiens (Human)
- Tissue: Optic nerve, Optic nerve head, Optic disc, Cranial nerve II
- Cell Type: Endothelial cells
- Technology: 10x Genomics 3' v3 snRNA-seq
- Condition: Normal
- Number of Cells: 34,934
- Associated CELLxGENE Collection ID:
05e3d0fc-c9dd-4f14-9163-2b242b3bb5c2
- Associated CELLxGENE Dataset ID:
f5b09167-e4b5-4f32-b7b4-f0b7c402a4c4
Dataset Structure
The dataset is provided in formats commonly used in single-cell genomics and tabular data analysis:
snRNA_seq_of_human_optic_nerve_and_optic_nerve_head_endothelial_cells.h5ad
: The primary AnnData object, encapsulating the gene expression matrix, cell metadata, and gene metadata. This is the most comprehensive format.expression.parquet
: A tabular representation of the gene expression matrix (corresponding toadata.X
), where rows are cells and columns are genes. Ideal for direct use in machine learning models.feature_metadata.parquet
: A tabular representation of the gene (feature) metadata (corresponding toadata.var
), providing details about each gene.
Data Cleaning and Processing
The raw data was accessed and retrieved via the cellxgene_census
API, which ensures standardized data types and preliminary quality control as part of the Census pipeline.
Further processing involved:
- Extraction of the relevant cell and gene metadata, ensuring appropriate data types for storage in
adata.obs
andadata.var
. - Conversion of the TileDB-SOMA object (from Census) into a standard AnnData object.
- Exporting the main expression matrix and gene metadata into Parquet format for broader compatibility with tabular data tools and machine learning frameworks.
The .h5ad
file specifically retains rich metadata from the Census, including organism, tissue, cell type annotations, and more, which can be leveraged for detailed analysis.
Usage
This dataset is ideal for a variety of research and machine learning tasks, including:
- Single-Cell Analysis: Exploring cellular heterogeneity, identifying novel cell states, and characterizing gene expression patterns in the optic nerve's endothelial cells.
- Aging Research: Investigating age-related changes in endothelial cell gene expression and function within the optic nerve, identifying biomarkers or therapeutic targets for age-related ocular diseases.
- Machine Learning: Developing models for cell type classification, dimensionality reduction, feature selection, and identifying gene signatures associated with specific biological states or aging phenotypes.
- Biomarker Discovery: Pinpointing genes or pathways implicated in optic nerve health and age-related visual impairment.
Download Instructions
You can download the files directly using the links below or with wget
/curl
.
File: snRNAseq_of_human_optic_nerve_and_optic_nerve_head_endothelial_cells.h5ad
Direct Link:
Download .h5adUsing
wget
:wget https://huggingface.co/datasets/Venkatachalam/snRNAseq_of_human_optic_nerve_and_optic_nerve_head_endothelial_cells/resolve/main/snRNAseq_of_human_optic_nerve_and_optic_nerve_head_endothelial_cells.h5ad
Citation
Please ensure you cite the original source of the data from CELLxGENE Discover. The specific publication for this dataset (GSE67547) can be found on its NCBI GEO page:
NCBI GEO Accession: GSE67547
When using the cellxgene_census API, you may also consider citing the Census project: https://chanzuckerberg.com/science/projects/single-cell-biology/cellxgene/cellxgene-census/
Contact
For questions or feedback regarding this processed dataset, please contact:
Venkatachalam, Pooja, Albert
Generated by cellVPA on June 14, 2025
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