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Single-cell RNA sequencing
Single-nucleus RNA sequencing
Single-cell Multiome
Single-cell TCR/BCR sequencing
Surface proteomics
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Xenium In Situ
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Bio-informatics
CytoNavigator™
Sample Whole-Process Monitoring System
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Immunology Research
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency
2025-11-12
上一篇:Endothelial response to type I interferon contributes to vasculopathy and fibrosis and predicts disease progression of systemic sclerosis
下一篇:Multiomics analyses reveal a critical role of selenium in controlling T cell differentiation in Crohn’s disease
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