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Dryad

Distinct T cell functions enable efficient immunoediting and prevent tumor emergence in developing sarcomas

Abstract

5’scRNA-seq from sorted live singlet CD45- CD31- TER119- tdTomato+ cells of KPFRT CreER/Ai65 RagWT, KPFRT CreER/Ai65 Rag KO, and KWT PFRT CreER/Ai65 RagWT mice was performed with each sample in its own sequencing lane on an Illumina Novaseq, was processed with Cell Ranger 9.0.0 using the mm10 mouse genome indices from 10X Genomics. We then used R (v4.4.1) with Seurat (v5.2.1) for preprocessing and analysis. Cells with greater than 200 features and less than 10% mitochondrial reads were included. RNA data was normalized, scaled, and principal components were found. The functions FindNeighbors, FindClusters, and RunUMAP were then run using principal components 1-15 and a resolution of 0.5. The packages ggplot2 (v3.5.2), ggpubr (v0.6.0), and dittoseq (v1.16.0) were used for visualizations.