This is a preprint.
Universal preprocessing of single-cell genomics data
- PMID: 37745572
- PMCID: PMC10515959
- DOI: 10.1101/2023.09.14.543267
Universal preprocessing of single-cell genomics data
Abstract
We describe a workflow for preprocessing a wide variety of single-cell genomics data types. The approach is based on parsing of machine-readable seqspec assay specifications to customize inputs for kb-python, which uses kallisto and bustools to catalog reads, error correct barcodes, and count reads. The universal preprocessing method is implemented in the Python package cellatlas that is available for download at: https://github.com/cellatlas/cellatlas/.
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References
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- Bray Nicolas L., Pimentel Harold, Melsted Páll, and Pachter Lior. 2016. “Near-Optimal Probabilistic RNA-Seq Quantification.” Nature Biotechnology 34 (5): 525–27. - PubMed
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