Figure 1.
Figure 1. Schematic representation of sample collection, processing, and TCR sequencing. Four-millimeter punch biopsies were collected from early lesions (plaques; red circles) or tumors (green squares) in 27 patients with MF. Biopsies were cryosectioned and laser microdissected to capture tumor cells that were pooled together. Original magnification ×10; hematoxylin and eosin staining. DNA and RNA were isolated simultaneously from the microdissected material and processed for WES and WTS. WTS data are available only for samples MF4_2T, MF4_3P, MF5_1T, MF5_2P, MF7_1T, MF7_2P, MF11T, MF11_1P, MF19_1T, and MF19_2P and a pool of normal CD4+ lymphocytes (data not shown). The gene sequence is indicated in green, the adapter sequence is indicated in red, and the index sequence is indicated in blue.

Schematic representation of sample collection, processing, and TCR sequencing. Four-millimeter punch biopsies were collected from early lesions (plaques; red circles) or tumors (green squares) in 27 patients with MF. Biopsies were cryosectioned and laser microdissected to capture tumor cells that were pooled together. Original magnification ×10; hematoxylin and eosin staining. DNA and RNA were isolated simultaneously from the microdissected material and processed for WES and WTS. WTS data are available only for samples MF4_2T, MF4_3P, MF5_1T, MF5_2P, MF7_1T, MF7_2P, MF11T, MF11_1P, MF19_1T, and MF19_2P and a pool of normal CD4+ lymphocytes (data not shown). The gene sequence is indicated in green, the adapter sequence is indicated in red, and the index sequence is indicated in blue.

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