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Recommendations for depositing scRNA-seq datasets

For investigators and reviewers

  1. Require that analysts provide a metadata table containing cell-level metadata and a count matrix with RNA abundance measurements. The cell-level metadata should contain the cell identifiers present in the matrix and provide the inferred cell-type or other cell-level annotations described in the associated publication. A binary object saved from the analysis framework could also be supplied (.rds for R or .h5ad for Python).

  2. When reviewing single-cell sequencing studies, ensure that the authors have deposited the proper cell-level metadata alongside the raw data into a suitable repository (e.g. GEO, ArrayExpress).

  3. Encouraging previous depositors of single-cell sequencing data to update their records with cell-level metadata, if it was not included in the original submission.

For journals

  1. Include language about requirements/recommendation for external single-cell datasets to contain proper cell-level metadata.

  2. Ask reviewers to review material deposited to external data repositories.

For data repositories

  1. Public repositories should introduce a standardized annotation that specifies that the dataset contains single cell data. For GEO, commonly used single cell sequencing methods could be added to the library strategy annotation (e.g. scRNA-seq, snRNA-seq, CITE-seq, etc.).

  2. Updating submission guidelines to require metadata with cell-level annotations for single cell dataset submissions. For GEO, this would be accomplished by updating the “Processed data files” requirements to outline required data types for single-cell sequencing submissions.

“For single-cell sequencing data, in addition to standard count matrices (genes-by-cells), we expect users to deposit metadata with cell-level annotations generated during the course of analysis.”

For more detailed discussions, please see:

  1. Füllgrabe et al
  2. Single Cell Portal Metadata Convention