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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)

Japan Agency for Medical Research and Development (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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