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LAMP: disease classification derived from layered assessment on modules and pathways in the human gene network

BACKGROUND: Classification of diseases based on genetic information is of great significance as the basis for precision medicine, increasing the understanding of disease etiology and revolutionizing personalized medicine. Much effort has been directed at understanding disease associations by constru...

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Autores principales: Mi, Zhilong, Guo, Binghui, Yang, Xiaobo, Yin, Ziqiao, Zheng, Zhiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7597061/
https://www.ncbi.nlm.nih.gov/pubmed/33126852
http://dx.doi.org/10.1186/s12859-020-03800-2
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author Mi, Zhilong
Guo, Binghui
Yang, Xiaobo
Yin, Ziqiao
Zheng, Zhiming
author_facet Mi, Zhilong
Guo, Binghui
Yang, Xiaobo
Yin, Ziqiao
Zheng, Zhiming
author_sort Mi, Zhilong
collection PubMed
description BACKGROUND: Classification of diseases based on genetic information is of great significance as the basis for precision medicine, increasing the understanding of disease etiology and revolutionizing personalized medicine. Much effort has been directed at understanding disease associations by constructing disease networks, and classifying patient samples according to gene expression data. Integrating human gene networks overcomes limited coverage of genes. Incorporating pathway information into disease classification procedure addresses the challenge of cellular heterogeneity across patients. RESULTS: In this work, we propose a disease classification model LAMP, which concentrates on the layered assessment on modules and pathways. Directed human gene interactions are the foundation of constructing the human gene network, where the significant roles of disease and pathway genes are recognized. The fast unfolding algorithm identifies 11 modules in the largest connected component. Then layered networks are introduced to distinguish positions of genes in propagating information from sources to targets. After gene screening, hierarchical clustering and refined process, 1726 diseases from KEGG are classified into 18 categories. Also, it is expounded that diseases with overlapping genes may not belong to the same category in LAMP. Within each category, entropy is applied to measure the compositional complexity, and to evaluate the prospects for combination diagnosis and gene-targeted therapy for diseases. CONCLUSION: In this work, by collecting data from BioGRID and KEGG, we develop a disease classification model LAMP, to support people to view diseases from the perspective of commonalities in etiology and pathology. Comprehensive research on existing diseases can help meet the challenges of unknown diseases. The results provide suggestions for combination diagnosis and gene-targeted therapy, which motivates clinicians and researchers to reposition the understanding of diseases and explore diagnosis and therapy strategies.
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spelling pubmed-75970612020-11-02 LAMP: disease classification derived from layered assessment on modules and pathways in the human gene network Mi, Zhilong Guo, Binghui Yang, Xiaobo Yin, Ziqiao Zheng, Zhiming BMC Bioinformatics Methodology Article BACKGROUND: Classification of diseases based on genetic information is of great significance as the basis for precision medicine, increasing the understanding of disease etiology and revolutionizing personalized medicine. Much effort has been directed at understanding disease associations by constructing disease networks, and classifying patient samples according to gene expression data. Integrating human gene networks overcomes limited coverage of genes. Incorporating pathway information into disease classification procedure addresses the challenge of cellular heterogeneity across patients. RESULTS: In this work, we propose a disease classification model LAMP, which concentrates on the layered assessment on modules and pathways. Directed human gene interactions are the foundation of constructing the human gene network, where the significant roles of disease and pathway genes are recognized. The fast unfolding algorithm identifies 11 modules in the largest connected component. Then layered networks are introduced to distinguish positions of genes in propagating information from sources to targets. After gene screening, hierarchical clustering and refined process, 1726 diseases from KEGG are classified into 18 categories. Also, it is expounded that diseases with overlapping genes may not belong to the same category in LAMP. Within each category, entropy is applied to measure the compositional complexity, and to evaluate the prospects for combination diagnosis and gene-targeted therapy for diseases. CONCLUSION: In this work, by collecting data from BioGRID and KEGG, we develop a disease classification model LAMP, to support people to view diseases from the perspective of commonalities in etiology and pathology. Comprehensive research on existing diseases can help meet the challenges of unknown diseases. The results provide suggestions for combination diagnosis and gene-targeted therapy, which motivates clinicians and researchers to reposition the understanding of diseases and explore diagnosis and therapy strategies. BioMed Central 2020-10-30 /pmc/articles/PMC7597061/ /pubmed/33126852 http://dx.doi.org/10.1186/s12859-020-03800-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology Article
Mi, Zhilong
Guo, Binghui
Yang, Xiaobo
Yin, Ziqiao
Zheng, Zhiming
LAMP: disease classification derived from layered assessment on modules and pathways in the human gene network
title LAMP: disease classification derived from layered assessment on modules and pathways in the human gene network
title_full LAMP: disease classification derived from layered assessment on modules and pathways in the human gene network
title_fullStr LAMP: disease classification derived from layered assessment on modules and pathways in the human gene network
title_full_unstemmed LAMP: disease classification derived from layered assessment on modules and pathways in the human gene network
title_short LAMP: disease classification derived from layered assessment on modules and pathways in the human gene network
title_sort lamp: disease classification derived from layered assessment on modules and pathways in the human gene network
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7597061/
https://www.ncbi.nlm.nih.gov/pubmed/33126852
http://dx.doi.org/10.1186/s12859-020-03800-2
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