Automated single-cell omics end-to-end framework with data-driven batch inference
Yuan WangiD, William ThistlethwaiteiD, Alicja TadychiD, Frederique Murielle Ruf-ZamojskiiD, Daniel J. BernardiD, Antonio CappuccioiD, Elena ZaslavskyiD, Xi CheniD, Stuart C. SealfoniD, Olga G. TroyanskayaiD
Abstract
To facilitate single-cell multi-omics analysis and improve reproducibility, we present SPEEDI (Single-cell Pipeline for End to End Data Integration), a fully automated end-to-end framework for batch inference, data integration, and cell type labeling. SPEEDI introduces data-driven batch inference and transforms the often heterogeneous data matrices obtained from different samples into a uniformly annotated and integrated dataset. Without requiring user input, it automatically selects parameters and executes pre-processing, sample integration, and cell type mapping. It can also perform downstream analyses of differential signals between treatment conditions and gene functional modules. SPEEDIs data-driven batch inference method works with widely used integration and cell-typing tools. By developing data-driven batch inference, providing full end-to-end automation, and eliminating parameter selection, SPEEDI improves reproducibility and lowers the barrier to obtaining biological insight from these valuable single-cell datasets. The SPEEDI interactive web application can be accessed at https://speedi.princeton.edu/.
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