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Processed Signatures

This page hosts our in-house single-cell RNA (scRNA) signatures for various applications. Below, you will find details about the processed signatures, including their source, cell type information, gene count, and download links.


Available Signatures

DatasetLevelNumber of Cell TypesKey Cell TypesTotal GenesSourceDownload
Lung Cancer SignatureLevel 1 (Major)PlaceholderEpithelial, Immune, StromalPlaceholderFigshareDownload
Level 2 (Subtypes)PlaceholderBasal, Luminal, T Cells, FibroblastsPlaceholderFigshare
Level 3 (Detailed)PlaceholderCD4+ T cells, CD8+ T cells, CAFsPlaceholderFigshare

Signature File Contents

Each signature file is provided in a pickle format (.pickle) and contains the following data:

  1. Gene-Level Statistics:

    • Mean Expression: Average gene expression values across all cells for each cell type.
    • Variance: Variability in expression for each gene across cells.
    • Standard Deviation: Standard deviation of gene expression for each gene within each cell type.
  2. Gene Lists:

    • Total Genes: The total number of genes included in the dataset.
    • Highly Variable Genes (HVGs): Genes identified as highly variable, which contribute significantly to the analysis.
    • Differentially Expressed Genes (DEGs): Genes selected by AutoGenes, including the number of DEGs identified.
  3. Cell Types:

    • A complete list of cell types present in the dataset, organized by hierarchical levels (e.g., major, subtype, detailed).

How to Use

  1. Select the desired signature from the table above.

  2. Click the Download button to access the file.

  3. Use the appropriate level based on your analysis requirements:

    • Level 1 (Major): Broad categories of cell types.
    • Level 2 (Subtypes): Subdivisions within major categories.
    • Level 3 (Detailed): Detailed classification of cell types.
  4. Refer to the [Tutorial] for guidance on using these signatures in your workflows.


Notes

  • The pickle file is Python-compatible. Users of other programming environments (e.g., R) may need to convert the file using a Python script.
  • Ensure that gene identifiers in the signature match those in your bulk RNA-seq data to avoid discrepancies during analysis.
  • This page will be regularly updated as new signatures are added. If you have feedback or specific requests, please contact us.

Feedback: For specific datasets or additional levels of detail, please reach out to our team through the contact form on the main site.