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NeuroTransDB: highly curated and structured transcriptomic metadata for neurodegenerative diseases

Neurodegenerative diseases are chronic debilitating conditions, characterized by progressive loss of neurons that represent a significant health care burden as the global elderly population continues to grow. Over the past decade, high-throughput technologies such as the Affymetrix GeneChip microarr...

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Autores principales: Bagewadi, Shweta, Adhikari, Subash, Dhrangadhariya, Anjani, Irin, Afroza Khanam, Ebeling, Christian, Namasivayam, Aishwarya Alex, Page, Matthew, Hofmann-Apitius, Martin, Senger, Philipp
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608514/
https://www.ncbi.nlm.nih.gov/pubmed/26475471
http://dx.doi.org/10.1093/database/bav099
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author Bagewadi, Shweta
Adhikari, Subash
Dhrangadhariya, Anjani
Irin, Afroza Khanam
Ebeling, Christian
Namasivayam, Aishwarya Alex
Page, Matthew
Hofmann-Apitius, Martin
Senger, Philipp
author_facet Bagewadi, Shweta
Adhikari, Subash
Dhrangadhariya, Anjani
Irin, Afroza Khanam
Ebeling, Christian
Namasivayam, Aishwarya Alex
Page, Matthew
Hofmann-Apitius, Martin
Senger, Philipp
author_sort Bagewadi, Shweta
collection PubMed
description Neurodegenerative diseases are chronic debilitating conditions, characterized by progressive loss of neurons that represent a significant health care burden as the global elderly population continues to grow. Over the past decade, high-throughput technologies such as the Affymetrix GeneChip microarrays have provided new perspectives into the pathomechanisms underlying neurodegeneration. Public transcriptomic data repositories, namely Gene Expression Omnibus and curated ArrayExpress, enable researchers to conduct integrative meta-analysis; increasing the power to detect differentially regulated genes in disease and explore patterns of gene dysregulation across biologically related studies. The reliability of retrospective, large-scale integrative analyses depends on an appropriate combination of related datasets, in turn requiring detailed meta-annotations capturing the experimental setup. In most cases, we observe huge variation in compliance to defined standards for submitted metadata in public databases. Much of the information to complete, or refine meta-annotations are distributed in the associated publications. For example, tissue preparation or comorbidity information is frequently described in an article’s supplementary tables. Several value-added databases have employed additional manual efforts to overcome this limitation. However, none of these databases explicate annotations that distinguish human and animal models in neurodegeneration context. Therefore, adopting a more specific disease focus, in combination with dedicated disease ontologies, will better empower the selection of comparable studies with refined annotations to address the research question at hand. In this article, we describe the detailed development of NeuroTransDB, a manually curated database containing metadata annotations for neurodegenerative studies. The database contains more than 20 dimensions of metadata annotations within 31 mouse, 5 rat and 45 human studies, defined in collaboration with domain disease experts. We elucidate the step-by-step guidelines used to critically prioritize studies from public archives and their metadata curation and discuss the key challenges encountered. Curated metadata for Alzheimer’s disease gene expression studies are available for download. Database URL: www.scai.fraunhofer.de/NeuroTransDB.html
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spelling pubmed-46085142015-10-19 NeuroTransDB: highly curated and structured transcriptomic metadata for neurodegenerative diseases Bagewadi, Shweta Adhikari, Subash Dhrangadhariya, Anjani Irin, Afroza Khanam Ebeling, Christian Namasivayam, Aishwarya Alex Page, Matthew Hofmann-Apitius, Martin Senger, Philipp Database (Oxford) Original Article Neurodegenerative diseases are chronic debilitating conditions, characterized by progressive loss of neurons that represent a significant health care burden as the global elderly population continues to grow. Over the past decade, high-throughput technologies such as the Affymetrix GeneChip microarrays have provided new perspectives into the pathomechanisms underlying neurodegeneration. Public transcriptomic data repositories, namely Gene Expression Omnibus and curated ArrayExpress, enable researchers to conduct integrative meta-analysis; increasing the power to detect differentially regulated genes in disease and explore patterns of gene dysregulation across biologically related studies. The reliability of retrospective, large-scale integrative analyses depends on an appropriate combination of related datasets, in turn requiring detailed meta-annotations capturing the experimental setup. In most cases, we observe huge variation in compliance to defined standards for submitted metadata in public databases. Much of the information to complete, or refine meta-annotations are distributed in the associated publications. For example, tissue preparation or comorbidity information is frequently described in an article’s supplementary tables. Several value-added databases have employed additional manual efforts to overcome this limitation. However, none of these databases explicate annotations that distinguish human and animal models in neurodegeneration context. Therefore, adopting a more specific disease focus, in combination with dedicated disease ontologies, will better empower the selection of comparable studies with refined annotations to address the research question at hand. In this article, we describe the detailed development of NeuroTransDB, a manually curated database containing metadata annotations for neurodegenerative studies. The database contains more than 20 dimensions of metadata annotations within 31 mouse, 5 rat and 45 human studies, defined in collaboration with domain disease experts. We elucidate the step-by-step guidelines used to critically prioritize studies from public archives and their metadata curation and discuss the key challenges encountered. Curated metadata for Alzheimer’s disease gene expression studies are available for download. Database URL: www.scai.fraunhofer.de/NeuroTransDB.html Oxford University Press 2015-10-15 /pmc/articles/PMC4608514/ /pubmed/26475471 http://dx.doi.org/10.1093/database/bav099 Text en © The Author(s) 2015. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://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 Article
Bagewadi, Shweta
Adhikari, Subash
Dhrangadhariya, Anjani
Irin, Afroza Khanam
Ebeling, Christian
Namasivayam, Aishwarya Alex
Page, Matthew
Hofmann-Apitius, Martin
Senger, Philipp
NeuroTransDB: highly curated and structured transcriptomic metadata for neurodegenerative diseases
title NeuroTransDB: highly curated and structured transcriptomic metadata for neurodegenerative diseases
title_full NeuroTransDB: highly curated and structured transcriptomic metadata for neurodegenerative diseases
title_fullStr NeuroTransDB: highly curated and structured transcriptomic metadata for neurodegenerative diseases
title_full_unstemmed NeuroTransDB: highly curated and structured transcriptomic metadata for neurodegenerative diseases
title_short NeuroTransDB: highly curated and structured transcriptomic metadata for neurodegenerative diseases
title_sort neurotransdb: highly curated and structured transcriptomic metadata for neurodegenerative diseases
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608514/
https://www.ncbi.nlm.nih.gov/pubmed/26475471
http://dx.doi.org/10.1093/database/bav099
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