![]() In Seurat v5, we also introduce flexible and streamlined workflows for the integration of multiple scRNA-seq datasets. We recognize that while the goal of matching shared cell types across datasets may be important for many problems, users may also be concerned about which method to use, or that integration could result in a loss of biological resolution. For example, we demonstrate how to map scATAC-seq datasets onto scRNA-seq datasets, to assist users in interpreting and annotating data from new modalities. In Seurat v5, we introduce ‘bridge integration’, a statistical method to integrate experiments measuring different modalities (i.e. separate scRNA-seq and scATAC-seq datasets), using a separate multiomic dataset as a molecular ‘bridge’. Integrative multimodal analysis: The cellular transcriptome is just one aspect of cellular identity, and recent technologies enable routine profiling of chromatin accessibility, histone modifications, and protein levels from single cells. Vignette: Analysis of spatial datasets (Imaging-based).Vignette: Analysis of spatial datasets (Sequencing-based).In Seurat v5, we introduce flexible and diverse support for a wide variety of spatially resolved data types, and support for analytical techniqiues for scRNA-seq integration, deconvolution, and niche identification. Both sequencing-based(i.e. Visium, SLIDE-seq, etc.), and imaging-based (MERFISH/Vizgen, Xenium, CosMX, etc.) technologies have unique advantages, and require tailored analytical methods and software infrastructure. ![]() We are excited to release an initial beta version of Seurat v5! This update brings the following new features and functionality:Īnalysis of sequencing and imaging-based spatial datasets: Spatially resolved datasets are redefining our understanding of cellular interactions and the organization of human tissues. ![]()
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