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. Author manuscript; available in PMC: 2023 Mar 1.
Published in final edited form as: Cancer Cytopathol. 2021 Nov 15;130(3):231–237. doi: 10.1002/cncy.22531

Figure 2.

Figure 2.

Visualization of high-dimensional flow cytometry data analyzed by the dimensional-reduction algorithm, viSNE. Cells are clustered by surface phenotypes: CD3+ T cells (blue), CD56+ NK cells (orange), CD14+ macrophages or monocytes (purple) and CD33+ granulocytes (brown). CD19+ B cells are split between Lambda- tumor cells (green) and Lambda+ normal B cells (red). (A) Example of 2 separate FNA from 2 different sites of a follicular lymphoma patient. (B) Single-cell suspension of a surgical biopsy from the same patient. (C) FNA performed on the biopsy ex vivo and prior to dissociation. (D) Example of peripheral blood drawn at the same time as the FNA.