Moreover, the researchers evaluated the mutational profile of MPN patients using next-generation sequencing in both DNA samples extracted from granulocytes and cfDNA and evidenced that cfDNA was as accurate as granulocyte DNA for the detection of driver (JAK2, CALR, MPL) and non-driver (TET2, ASXL1, IDH2, DNMT3A, SF3B1, SRSF2, etc.)mutations. Here, DNMT3A is linked to myeloproliferative disorder.