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Detection of genome-wide copy number variants in myeloid malignancies using next-generation sequencing
- 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
Citation
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.
Online issue publication
August 11, 2020
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- Previous version (20 March 2018).
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© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.