Cargando…
Precise characterization of somatic complex structural variations from tumor/control paired long-read sequencing data with nanomonsv
We present our novel software, nanomonsv, for detecting somatic structural variations (SVs) using tumor and matched control long-read sequencing data with a single-base resolution. The current version of nanomonsv includes two detection modules, Canonical SV module, and Single breakend SV module. Us...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415145/ https://www.ncbi.nlm.nih.gov/pubmed/37336583 http://dx.doi.org/10.1093/nar/gkad526 |
_version_ | 1785087457725775872 |
---|---|
author | Shiraishi, Yuichi Koya, Junji Chiba, Kenichi Okada, Ai Arai, Yasuhito Saito, Yuki Shibata, Tatsuhiro Kataoka, Keisuke |
author_facet | Shiraishi, Yuichi Koya, Junji Chiba, Kenichi Okada, Ai Arai, Yasuhito Saito, Yuki Shibata, Tatsuhiro Kataoka, Keisuke |
author_sort | Shiraishi, Yuichi |
collection | PubMed |
description | We present our novel software, nanomonsv, for detecting somatic structural variations (SVs) using tumor and matched control long-read sequencing data with a single-base resolution. The current version of nanomonsv includes two detection modules, Canonical SV module, and Single breakend SV module. Using tumor/control paired long-read sequencing data from three cancer and their matched lymphoblastoid lines, we demonstrate that Canonical SV module can identify somatic SVs that can be captured by short-read technologies with higher precision and recall than existing methods. In addition, we have developed a workflow to classify mobile element insertions while elucidating their in-depth properties, such as 5′ truncations, internal inversions, as well as source sites for 3′ transductions. Furthermore, Single breakend SV module enables the detection of complex SVs that can only be identified by long-reads, such as SVs involving highly-repetitive centromeric sequences, and LINE1- and virus-mediated rearrangements. In summary, our approaches applied to cancer long-read sequencing data can reveal various features of somatic SVs and will lead to a better understanding of mutational processes and functional consequences of somatic SVs. |
format | Online Article Text |
id | pubmed-10415145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-104151452023-08-12 Precise characterization of somatic complex structural variations from tumor/control paired long-read sequencing data with nanomonsv Shiraishi, Yuichi Koya, Junji Chiba, Kenichi Okada, Ai Arai, Yasuhito Saito, Yuki Shibata, Tatsuhiro Kataoka, Keisuke Nucleic Acids Res Methods We present our novel software, nanomonsv, for detecting somatic structural variations (SVs) using tumor and matched control long-read sequencing data with a single-base resolution. The current version of nanomonsv includes two detection modules, Canonical SV module, and Single breakend SV module. Using tumor/control paired long-read sequencing data from three cancer and their matched lymphoblastoid lines, we demonstrate that Canonical SV module can identify somatic SVs that can be captured by short-read technologies with higher precision and recall than existing methods. In addition, we have developed a workflow to classify mobile element insertions while elucidating their in-depth properties, such as 5′ truncations, internal inversions, as well as source sites for 3′ transductions. Furthermore, Single breakend SV module enables the detection of complex SVs that can only be identified by long-reads, such as SVs involving highly-repetitive centromeric sequences, and LINE1- and virus-mediated rearrangements. In summary, our approaches applied to cancer long-read sequencing data can reveal various features of somatic SVs and will lead to a better understanding of mutational processes and functional consequences of somatic SVs. Oxford University Press 2023-06-20 /pmc/articles/PMC10415145/ /pubmed/37336583 http://dx.doi.org/10.1093/nar/gkad526 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Shiraishi, Yuichi Koya, Junji Chiba, Kenichi Okada, Ai Arai, Yasuhito Saito, Yuki Shibata, Tatsuhiro Kataoka, Keisuke Precise characterization of somatic complex structural variations from tumor/control paired long-read sequencing data with nanomonsv |
title | Precise characterization of somatic complex structural variations from tumor/control paired long-read sequencing data with nanomonsv |
title_full | Precise characterization of somatic complex structural variations from tumor/control paired long-read sequencing data with nanomonsv |
title_fullStr | Precise characterization of somatic complex structural variations from tumor/control paired long-read sequencing data with nanomonsv |
title_full_unstemmed | Precise characterization of somatic complex structural variations from tumor/control paired long-read sequencing data with nanomonsv |
title_short | Precise characterization of somatic complex structural variations from tumor/control paired long-read sequencing data with nanomonsv |
title_sort | precise characterization of somatic complex structural variations from tumor/control paired long-read sequencing data with nanomonsv |
topic | Methods |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415145/ https://www.ncbi.nlm.nih.gov/pubmed/37336583 http://dx.doi.org/10.1093/nar/gkad526 |
work_keys_str_mv | AT shiraishiyuichi precisecharacterizationofsomaticcomplexstructuralvariationsfromtumorcontrolpairedlongreadsequencingdatawithnanomonsv AT koyajunji precisecharacterizationofsomaticcomplexstructuralvariationsfromtumorcontrolpairedlongreadsequencingdatawithnanomonsv AT chibakenichi precisecharacterizationofsomaticcomplexstructuralvariationsfromtumorcontrolpairedlongreadsequencingdatawithnanomonsv AT okadaai precisecharacterizationofsomaticcomplexstructuralvariationsfromtumorcontrolpairedlongreadsequencingdatawithnanomonsv AT araiyasuhito precisecharacterizationofsomaticcomplexstructuralvariationsfromtumorcontrolpairedlongreadsequencingdatawithnanomonsv AT saitoyuki precisecharacterizationofsomaticcomplexstructuralvariationsfromtumorcontrolpairedlongreadsequencingdatawithnanomonsv AT shibatatatsuhiro precisecharacterizationofsomaticcomplexstructuralvariationsfromtumorcontrolpairedlongreadsequencingdatawithnanomonsv AT kataokakeisuke precisecharacterizationofsomaticcomplexstructuralvariationsfromtumorcontrolpairedlongreadsequencingdatawithnanomonsv |