In patients where multiple samples were available for analysis, all of which passed quality control measures (HGBL-DH/TH and tnDLBCL) (n = 27) we detected a highly significant correlation between samples in terms of our previously defined clonality measures as well as regarding sequence homology ( Figure 2 A–D).
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Systemic Inflammation and Tumour-Infiltrating T-Cell Receptor Repertoire Diversity Are Predictive of Clinical Outcome in High-Grade B-Cell Lymphoma with <i>MYC</i> and <i>BCL2</i> and/or <i>BCL6</i> Rearrangements.
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