Genetic mutations detected in CLL patients

Genetic mutations were detected by targeted NGS panels or Sanger sequencing in 46 CLL patients. Total DNA from PB, BM or LN samples was extracted for targeted NGS to detect gene mutations. Targeted NGS was also performed using the Ion Torrent/Illumina NextSeq 550Dx and Illumina MiSeq platform. Sequencing data of the patients who carried positive results is listed here.