A sensitive PCR-based method was developed to produce B-cell clonogeni
c probes without the need for sequencing and specific oligonucleotide
synthesis. Specificity and sensitivity were assessed and found to be c
omparable to that achieved using established methods. Possible applica
tions include the detection of MRD, bone marrow involvement with lymph
oma, and the contamination of autologous bone marrow or peripheral blo
od progenitor cell harvests with malignant cells carrying IgH rearrang
ements.