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Chromothripsis detection with multiple myeloma patients based on deep graph learning
MOTIVATION: Chromothripsis, associated with poor clinical outcomes, is prognostically vital in multiple myeloma. The catastrophic event is reported to be detectable prior to the progression of multiple myeloma. As a result, chromothripsis detection can contribute to risk estimation and early treatme...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10343948/ https://www.ncbi.nlm.nih.gov/pubmed/37399092 http://dx.doi.org/10.1093/bioinformatics/btad422 |
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author | Yu, Jixiang Chen, Nanjun Zheng, Zetian Gao, Ming Liang, Ning Wong, Ka-Chun |
author_facet | Yu, Jixiang Chen, Nanjun Zheng, Zetian Gao, Ming Liang, Ning Wong, Ka-Chun |
author_sort | Yu, Jixiang |
collection | PubMed |
description | MOTIVATION: Chromothripsis, associated with poor clinical outcomes, is prognostically vital in multiple myeloma. The catastrophic event is reported to be detectable prior to the progression of multiple myeloma. As a result, chromothripsis detection can contribute to risk estimation and early treatment guidelines for multiple myeloma patients. However, manual diagnosis remains the gold standard approach to detect chromothripsis events with the whole-genome sequencing technology to retrieve both copy number variation (CNV) and structural variation data. Meanwhile, CNV data are much easier to obtain than structural variation data. Hence, in order to reduce the reliance on human experts’ efforts and structural variation data extraction, it is necessary to establish a reliable and accurate chromothripsis detection method based on CNV data. RESULTS: To address those issues, we propose a method to detect chromothripsis solely based on CNV data. With the help of structure learning, the intrinsic relationship-directed acyclic graph of CNV features is inferred to derive a CNV embedding graph (i.e. CNV-DAG). Subsequently, a neural network based on Graph Transformer, local feature extraction, and non-linear feature interaction, is proposed with the embedding graph as the input to distinguish whether the chromothripsis event occurs. Ablation experiments, clustering, and feature importance analysis are also conducted to enable the proposed model to be explained by capturing mechanistic insights. AVAILABILITY AND IMPLEMENTATION: The source code and data are freely available at https://github.com/luvyfdawnYu/CNV_chromothripsis. |
format | Online Article Text |
id | pubmed-10343948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103439482023-07-14 Chromothripsis detection with multiple myeloma patients based on deep graph learning Yu, Jixiang Chen, Nanjun Zheng, Zetian Gao, Ming Liang, Ning Wong, Ka-Chun Bioinformatics Original Paper MOTIVATION: Chromothripsis, associated with poor clinical outcomes, is prognostically vital in multiple myeloma. The catastrophic event is reported to be detectable prior to the progression of multiple myeloma. As a result, chromothripsis detection can contribute to risk estimation and early treatment guidelines for multiple myeloma patients. However, manual diagnosis remains the gold standard approach to detect chromothripsis events with the whole-genome sequencing technology to retrieve both copy number variation (CNV) and structural variation data. Meanwhile, CNV data are much easier to obtain than structural variation data. Hence, in order to reduce the reliance on human experts’ efforts and structural variation data extraction, it is necessary to establish a reliable and accurate chromothripsis detection method based on CNV data. RESULTS: To address those issues, we propose a method to detect chromothripsis solely based on CNV data. With the help of structure learning, the intrinsic relationship-directed acyclic graph of CNV features is inferred to derive a CNV embedding graph (i.e. CNV-DAG). Subsequently, a neural network based on Graph Transformer, local feature extraction, and non-linear feature interaction, is proposed with the embedding graph as the input to distinguish whether the chromothripsis event occurs. Ablation experiments, clustering, and feature importance analysis are also conducted to enable the proposed model to be explained by capturing mechanistic insights. AVAILABILITY AND IMPLEMENTATION: The source code and data are freely available at https://github.com/luvyfdawnYu/CNV_chromothripsis. Oxford University Press 2023-07-03 /pmc/articles/PMC10343948/ /pubmed/37399092 http://dx.doi.org/10.1093/bioinformatics/btad422 Text en © The Author(s) 2023. Published by Oxford University Press. 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 | Original Paper Yu, Jixiang Chen, Nanjun Zheng, Zetian Gao, Ming Liang, Ning Wong, Ka-Chun Chromothripsis detection with multiple myeloma patients based on deep graph learning |
title | Chromothripsis detection with multiple myeloma patients based on deep graph learning |
title_full | Chromothripsis detection with multiple myeloma patients based on deep graph learning |
title_fullStr | Chromothripsis detection with multiple myeloma patients based on deep graph learning |
title_full_unstemmed | Chromothripsis detection with multiple myeloma patients based on deep graph learning |
title_short | Chromothripsis detection with multiple myeloma patients based on deep graph learning |
title_sort | chromothripsis detection with multiple myeloma patients based on deep graph learning |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10343948/ https://www.ncbi.nlm.nih.gov/pubmed/37399092 http://dx.doi.org/10.1093/bioinformatics/btad422 |
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