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Universal preprocessing of single-cell genomics data

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....

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Detalles Bibliográficos
Autores principales: Booeshaghi, A. Sina, Sullivan, Delaney K., Pachter, Lior
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515959/
https://www.ncbi.nlm.nih.gov/pubmed/37745572
http://dx.doi.org/10.1101/2023.09.14.543267

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