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e-TSN: an interactive visual exploration platform for target–disease knowledge mapping from literature

Target discovery and identification processes are driven by the increasing amount of biomedical data. The vast numbers of unstructured texts of biomedical publications provide a rich source of knowledge for drug target discovery research and demand the development of specific algorithms or tools to...

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Detalles Bibliográficos
Autores principales: Feng, Ziyan, Shen, Zihao, Li, Honglin, Li, Shiliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9677481/
https://www.ncbi.nlm.nih.gov/pubmed/36347537
http://dx.doi.org/10.1093/bib/bbac465
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author Feng, Ziyan
Shen, Zihao
Li, Honglin
Li, Shiliang
author_facet Feng, Ziyan
Shen, Zihao
Li, Honglin
Li, Shiliang
author_sort Feng, Ziyan
collection PubMed
description Target discovery and identification processes are driven by the increasing amount of biomedical data. The vast numbers of unstructured texts of biomedical publications provide a rich source of knowledge for drug target discovery research and demand the development of specific algorithms or tools to facilitate finding disease genes and proteins. Text mining is a method that can automatically mine helpful information related to drug target discovery from massive biomedical literature. However, there is a substantial lag between biomedical publications and the subsequent abstraction of information extracted by text mining to databases. The knowledge graph is introduced to integrate heterogeneous biomedical data. Here, we describe e-TSN (Target significance and novelty explorer, http://www.lilab-ecust.cn/etsn/), a knowledge visualization web server integrating the largest database of associations between targets and diseases from the full scientific literature by constructing significance and novelty scoring methods based on bibliometric statistics. The platform aims to visualize target–disease knowledge graphs to assist in prioritizing candidate disease-related proteins. Approved drugs and associated bioactivities for each interested target are also provided to facilitate the visualization of drug–target relationships. In summary, e-TSN is a fast and customizable visualization resource for investigating and analyzing the intricate target–disease networks, which could help researchers understand the mechanisms underlying complex disease phenotypes and improve the drug discovery and development efficiency, especially for the unexpected outbreak of infectious disease pandemics like COVID-19.
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spelling pubmed-96774812022-11-21 e-TSN: an interactive visual exploration platform for target–disease knowledge mapping from literature Feng, Ziyan Shen, Zihao Li, Honglin Li, Shiliang Brief Bioinform Problem Solving Protocol Target discovery and identification processes are driven by the increasing amount of biomedical data. The vast numbers of unstructured texts of biomedical publications provide a rich source of knowledge for drug target discovery research and demand the development of specific algorithms or tools to facilitate finding disease genes and proteins. Text mining is a method that can automatically mine helpful information related to drug target discovery from massive biomedical literature. However, there is a substantial lag between biomedical publications and the subsequent abstraction of information extracted by text mining to databases. The knowledge graph is introduced to integrate heterogeneous biomedical data. Here, we describe e-TSN (Target significance and novelty explorer, http://www.lilab-ecust.cn/etsn/), a knowledge visualization web server integrating the largest database of associations between targets and diseases from the full scientific literature by constructing significance and novelty scoring methods based on bibliometric statistics. The platform aims to visualize target–disease knowledge graphs to assist in prioritizing candidate disease-related proteins. Approved drugs and associated bioactivities for each interested target are also provided to facilitate the visualization of drug–target relationships. In summary, e-TSN is a fast and customizable visualization resource for investigating and analyzing the intricate target–disease networks, which could help researchers understand the mechanisms underlying complex disease phenotypes and improve the drug discovery and development efficiency, especially for the unexpected outbreak of infectious disease pandemics like COVID-19. Oxford University Press 2022-11-08 /pmc/articles/PMC9677481/ /pubmed/36347537 http://dx.doi.org/10.1093/bib/bbac465 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Problem Solving Protocol
Feng, Ziyan
Shen, Zihao
Li, Honglin
Li, Shiliang
e-TSN: an interactive visual exploration platform for target–disease knowledge mapping from literature
title e-TSN: an interactive visual exploration platform for target–disease knowledge mapping from literature
title_full e-TSN: an interactive visual exploration platform for target–disease knowledge mapping from literature
title_fullStr e-TSN: an interactive visual exploration platform for target–disease knowledge mapping from literature
title_full_unstemmed e-TSN: an interactive visual exploration platform for target–disease knowledge mapping from literature
title_short e-TSN: an interactive visual exploration platform for target–disease knowledge mapping from literature
title_sort e-tsn: an interactive visual exploration platform for target–disease knowledge mapping from literature
topic Problem Solving Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9677481/
https://www.ncbi.nlm.nih.gov/pubmed/36347537
http://dx.doi.org/10.1093/bib/bbac465
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