In this issue of Blood, Soverini et al demonstrate the benefits of ultra-deep sequencing (UDS) compared with conventional Sanger sequencing in detecting BCR-ABL kinase domain mutations. This might improve tailoring of the treatment for resistant patients with chronic myeloid leukemia and Ph + acute lymphoblastic leukemia (Ph+ ALL) in the future.
CITATION STYLE
Müller, M. C. (2013, August 29). The ne plus ultra for deep BCR-ABL sequencing? Blood. American Society of Hematology. https://doi.org/10.1182/blood-2013-07-510958
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