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Foundational platforms such as Scanpy 114 and Seurat 115 are indispensable for the initial preprocessing, clustering and visualization of single-cell RNA sequencing (scRNA-seq) data, enabling the dissection of myeloid cell heterogeneity 116,117

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Other limitations involve our methods with PBMC lysates being used for cytokine measurements

Upon UV activation, the arylazide forms covalent bonds with labelled proteins, anchoring the probe and enabling downstream protein identification vi a high-throughput proteomics (Fig