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. 2017 Sep 14;8:1157. doi: 10.3389/fimmu.2017.01157

Figure 5.

Figure 5

Identification of chronic lymphocytic leukemia (CLL) spike-in upon dilution. (A) CLL spike-in was performed as in Figure 4A. The ds-cDNA obtained from a CLL spike-in with 1 cell per CLL was diluted at different levels (1:1, 1:2, 1:4, 1:8, and 1:16) to simulate genetic material dilution before PCR amplification step. (B) Impact of the dilution of genetic material on the identification of specific CLL IGHV genes. Every fraction of the three different replicates was sequenced. (C) The UMIG count of CLL spike-in correlates with the detection frequency after 1:16 dilution.