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Quantification of subclonal selection in cancer from bulk sequencing data

Crossref DOI link: https://doi.org/10.1038/s41588-018-0128-6

Published Online: 2018-05-28

Published Print: 2018-06

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Williams, Marc J. https://orcid.org/0000-0001-5524-4174
Werner, Benjamin

Heide, Timon https://orcid.org/0000-0002-1386-7469
Curtis, Christina https://orcid.org/0000-0003-0166-3802
Barnes, Chris P. https://orcid.org/0000-0002-9459-1395
Sottoriva, Andrea https://orcid.org/0000-0001-6709-9533
Graham, Trevor A. https://orcid.org/0000-0001-9582-1597
License Information

Text and Data Mining valid from 2018-05-28
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Article History

Received: 19 May 2017

Accepted: 23 March 2018

First Online: 28 May 2018

Change Date: 18 July 2018

Change Type: Correction

Change Details: In the version of this article originally published, in the “Theoretical framework of subclonal selection” section of the main text, ref. 11 instead of ref. 19 should have been cited at the end of the phrase “Our previously presented frequentist approach to detect subclonal selection from bulk sequencing data involves anRtest statistic.” The error has been corrected in the HTML and PDF versions of the article.

Competing interests

: The authors declare no competing interests.