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Concurrent detection of targeted copy number variants and mutations using a myeloid malignancy next generation sequencing panel allows comprehensive genetic analysis using a single testing strategy.
Shen W, Szankasi P, Sederberg M, Schumacher J, Frizzell KA, Gee EP, Patel JL, South ST, Xu X, Kelley TW. Shen W, et al. Among authors: sederberg m. Br J Haematol. 2016 Apr;173(1):49-58. doi: 10.1111/bjh.13921. Epub 2016 Jan 5. Br J Haematol. 2016. PMID: 26728869 Free article. Clinical Trial.