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Divide and Conquer: A Flexible Deep Learning Strategy for Exploring Metabolic Heterogeneity from Mass Spectrometry Imaging Data
[Image: see text] Research on metabolic heterogeneity provides an important basis for the study of the molecular mechanism of a disease and personalized treatment. The screening of metabolism-related sub-regions that affect disease development is essential for the more focused exploration on disease...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9878502/ https://www.ncbi.nlm.nih.gov/pubmed/36633187 http://dx.doi.org/10.1021/acs.analchem.2c04045 |
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author | Guo, Lei Dong, Jiyang Xu, Xiangnan Wu, Zhichao Zhang, Yinbin Wang, Yongwei Li, Pengfei Tang, Zhi Zhao, Chao Cai, Zongwei |
author_facet | Guo, Lei Dong, Jiyang Xu, Xiangnan Wu, Zhichao Zhang, Yinbin Wang, Yongwei Li, Pengfei Tang, Zhi Zhao, Chao Cai, Zongwei |
author_sort | Guo, Lei |
collection | PubMed |
description | [Image: see text] Research on metabolic heterogeneity provides an important basis for the study of the molecular mechanism of a disease and personalized treatment. The screening of metabolism-related sub-regions that affect disease development is essential for the more focused exploration on disease progress aberrant phenotypes, even carcinogenesis and metastasis. The mass spectrometry imaging (MSI) technique has distinct advantages to reveal the heterogeneity of an organism based on in situ molecular profiles. The challenge of heterogeneous analysis has been to perform an objective identification among biological tissues with different characteristics. By introducing the divide-and-conquer strategy to architecture design and application, we establish here a flexible unsupervised deep learning model, called divide-and-conquer (dc)-DeepMSI, for metabolic heterogeneity analysis from MSI data without prior knowledge of histology. dc-DeepMSI can be used to identify either spatially contiguous regions of interest (ROIs) or spatially sporadic ROIs by designing two specific modes, spat-contig and spat-spor. Comparison results on fetus mouse data demonstrate that the dc-DeepMSI outperforms state-of-the-art MSI segmentation methods. We demonstrate that the novel learning strategy successfully obtained sub-regions that are statistically linked to the invasion status and molecular phenotypes of breast cancer as well as organizing principles during developmental phase. |
format | Online Article Text |
id | pubmed-9878502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-98785022023-01-27 Divide and Conquer: A Flexible Deep Learning Strategy for Exploring Metabolic Heterogeneity from Mass Spectrometry Imaging Data Guo, Lei Dong, Jiyang Xu, Xiangnan Wu, Zhichao Zhang, Yinbin Wang, Yongwei Li, Pengfei Tang, Zhi Zhao, Chao Cai, Zongwei Anal Chem [Image: see text] Research on metabolic heterogeneity provides an important basis for the study of the molecular mechanism of a disease and personalized treatment. The screening of metabolism-related sub-regions that affect disease development is essential for the more focused exploration on disease progress aberrant phenotypes, even carcinogenesis and metastasis. The mass spectrometry imaging (MSI) technique has distinct advantages to reveal the heterogeneity of an organism based on in situ molecular profiles. The challenge of heterogeneous analysis has been to perform an objective identification among biological tissues with different characteristics. By introducing the divide-and-conquer strategy to architecture design and application, we establish here a flexible unsupervised deep learning model, called divide-and-conquer (dc)-DeepMSI, for metabolic heterogeneity analysis from MSI data without prior knowledge of histology. dc-DeepMSI can be used to identify either spatially contiguous regions of interest (ROIs) or spatially sporadic ROIs by designing two specific modes, spat-contig and spat-spor. Comparison results on fetus mouse data demonstrate that the dc-DeepMSI outperforms state-of-the-art MSI segmentation methods. We demonstrate that the novel learning strategy successfully obtained sub-regions that are statistically linked to the invasion status and molecular phenotypes of breast cancer as well as organizing principles during developmental phase. American Chemical Society 2023-01-12 /pmc/articles/PMC9878502/ /pubmed/36633187 http://dx.doi.org/10.1021/acs.analchem.2c04045 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Guo, Lei Dong, Jiyang Xu, Xiangnan Wu, Zhichao Zhang, Yinbin Wang, Yongwei Li, Pengfei Tang, Zhi Zhao, Chao Cai, Zongwei Divide and Conquer: A Flexible Deep Learning Strategy for Exploring Metabolic Heterogeneity from Mass Spectrometry Imaging Data |
title | Divide and
Conquer: A Flexible Deep Learning Strategy
for Exploring Metabolic Heterogeneity from Mass Spectrometry Imaging
Data |
title_full | Divide and
Conquer: A Flexible Deep Learning Strategy
for Exploring Metabolic Heterogeneity from Mass Spectrometry Imaging
Data |
title_fullStr | Divide and
Conquer: A Flexible Deep Learning Strategy
for Exploring Metabolic Heterogeneity from Mass Spectrometry Imaging
Data |
title_full_unstemmed | Divide and
Conquer: A Flexible Deep Learning Strategy
for Exploring Metabolic Heterogeneity from Mass Spectrometry Imaging
Data |
title_short | Divide and
Conquer: A Flexible Deep Learning Strategy
for Exploring Metabolic Heterogeneity from Mass Spectrometry Imaging
Data |
title_sort | divide and
conquer: a flexible deep learning strategy
for exploring metabolic heterogeneity from mass spectrometry imaging
data |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9878502/ https://www.ncbi.nlm.nih.gov/pubmed/36633187 http://dx.doi.org/10.1021/acs.analchem.2c04045 |
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