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Development and validation of a whole-exome sequencing test for simultaneous detection of point mutations, indels and copy-number alterations for precision cancer care

Crossref DOI link: https://doi.org/10.1038/npjgenmed.2016.19

Published Online: 2016-07-20

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

Authors

Rennert, Hanna

Eng, Kenneth

Zhang, Tuo

Tan, Adrian

Xiang, Jenny

Romanel, Alessandro

Kim, Robert

Tam, Wayne

Liu, Yen-Chun

Bhinder, Bhavneet

Cyrta, Joanna

Beltran, Himisha

Robinson, Brian

Mosquera, Juan Miguel

Fernandes, Helen

Demichelis, Francesca http://orcid.org/0000-0002-8266-8631
Sboner, Andrea

Kluk, Michael

Rubin, Mark A

Elemento, Olivier
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Text and Data Mining valid from 2016-07-20

Version of Record valid from 2016-07-20
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Article History

Received: 27 February 2016

Revised: 3 June 2016

Accepted: 7 June 2016

First Online: 20 July 2016

Competing interests

: The authors declare no conflict of interest.

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