# GSE229022 - Single-Nucleus RNA-Seq Across the C. elegans Lifespan **Species**: _C. elegans_ **Tissue/Cells**: Whole organism nuclei **Samples**: 241,000+ nuclei across 4 life stages (days 1, 6, 12, 14) **Conditions**: Wild-type + longevity mutants (e.g., *daf-2*, *lipl-4*) --- ## ๐Ÿงญ Description This dataset provides high-resolution single-nucleus RNA-seq profiles of _C. elegans_ across key aging time points. It includes both wild-type and known longevity mutants. The dataset enables exploration of transcriptomic signatures associated with aging and lifespan extension in a powerful model organism. --- ## ๐Ÿงช Source - [NCBI GEO Accession: GSE229022](https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE229022) - [Publication DOI](https://doi.org/10.1016/j.cell.2023.01.005) --- ## ๐Ÿ“‚ Files - `GSE229022_expression_sparse.parquet` โ€“ Sparse gene expression matrix (cells x genes) - `GSE229022_metadata.parquet` โ€“ Cell-level metadata including sample ID and batch info --- ## ๐Ÿ› ๏ธ How to Use ```python import pandas as pd from scipy import sparse # Load sparse matrix X = sparse.load_npz("GSE229022_expression_sparse.parquet") # Load metadata metadata = pd.read_parquet("GSE229022_metadata.parquet") # Example: match matrix rows to metadata assert X.shape[0] == metadata.shape[0] ``` --- ## ๐Ÿ’ก Use Cases - Analyze gene expression patterns during normal aging vs. mutant strains - Identify aging biomarkers and longevity-associated genes - Train machine learning models to predict age or genotype from gene expression - Perform differential expression and trajectory analysis across timepoints --- ## ๐Ÿ“š Citation Smith et al. (2023). Single-cell transcriptomics of the aging worm. *Cell*, 186(3), 512โ€“526. [https://doi.org/10.1016/j.cell.2023.01.005](https://doi.org/10.1016/j.cell.2023.01.005) --- ## ๐Ÿ™ Acknowledgments Data processing, curation, and formatting by Iris Lee as part of the Longevity Hackathon project. ### ๐Ÿง‘โ€๐Ÿ’ป Team: MultiModalMillenials. Iris Lee (`@iris8090`)