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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...

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Autores principales: Shiraishi, Yuichi, Koya, Junji, Chiba, Kenichi, Okada, Ai, Arai, Yasuhito, Saito, Yuki, Shibata, Tatsuhiro, Kataoka, Keisuke
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
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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.
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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
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