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Detection of genome-wide copy number variants in myeloid malignancies using next-generation sequencing

Authors

  1. Correspondence to Dr Xinjie Xu, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT 84108, USA; xinjie.xu{at}aruplab.com
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Citation

Shen W, Paxton CN, Szankasi P, et al
Detection of genome-wide copy number variants in myeloid malignancies using next-generation sequencing

Publication history

  • Received October 2, 2017
  • Revised November 1, 2017
  • Accepted November 16, 2017
  • First published December 2, 2017.

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