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Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer

Crossref DOI link: https://doi.org/10.1186/s13073-021-00883-1

Published Online: 2021-04-29

Published Print: 2021-12

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

Authors

Fujimoto, Akihiro https://orcid.org/0000-0002-0075-0800
Wong, Jing Hao

Yoshii, Yukiko

Akiyama, Shintaro

Tanaka, Azusa

Yagi, Hitomi

Shigemizu, Daichi

Nakagawa, Hidewaki

Mizokami, Masashi

Shimada, Mihoko
Funding

Funding for this research was provided by:

Japan Society for the Promotion of Science (18H02680)

Japan Agency for Medical Research and Development (18kk0205007h0003, 18km0405207h0003)

Ministry of Education, Culture, Sports, Science and Technology (18H05511)
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Text and Data Mining valid from 2021-04-29

Version of Record valid from 2021-04-29
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Article History

Received: 30 June 2020

Accepted: 6 April 2021

First Online: 29 April 2021

Declarations

:

: Informed consent to participate in the study was obtained from all subjects following the ICGC guidelines []. IRBs at RIKEN, Kyoto University, The University of Tokyo, and all groups participating in this study approved this work. This research conforms to the principles of the Helsinki Declaration.

: Not applicable.

: The authors declare that they have no competing interests.

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