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Mouse lymph node tissue was dissociated into a single nuclei solution with a Singulator 100 (S2 Genomics). The samples were strained, centrifuged, and resuspended in Nuclei Storage Buffer. The sample was split, and half of the sample was prepared with the 10x Genomics™ Next GEM Single Cell 3’ Kit v3.1. The remaining half was fixed with Evercode Cell Fixation v2 and shipped for further processing with Evercode WT v2. The sequencing data were processed with each manufacturer’s respective analysis pipeline.
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