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Alzheimer’s Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer’s Disease
BACKGROUND: Recent Alzheimer’s disease (AD) genetics findings from genome-wide association studies (GWAS) span progressively larger and more diverse populations and outcomes. Currently, there is no up-to-date resource providing harmonized and searchable information on all AD genetic associations fou...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9028687/ https://www.ncbi.nlm.nih.gov/pubmed/35068457 http://dx.doi.org/10.3233/JAD-215055 |
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author | Kuksa, Pavel P. Liu, Chia-Lun Fu, Wei Qu, Liming Zhao, Yi Katanic, Zivadin Clark, Kaylyn Kuzma, Amanda B. Ho, Pei-Chuan Tzeng, Kai-Teh Valladares, Otto Chou, Shin-Yi Naj, Adam C. Schellenberg, Gerard D. Wang, Li-San Leung, Yuk Yee |
author_facet | Kuksa, Pavel P. Liu, Chia-Lun Fu, Wei Qu, Liming Zhao, Yi Katanic, Zivadin Clark, Kaylyn Kuzma, Amanda B. Ho, Pei-Chuan Tzeng, Kai-Teh Valladares, Otto Chou, Shin-Yi Naj, Adam C. Schellenberg, Gerard D. Wang, Li-San Leung, Yuk Yee |
author_sort | Kuksa, Pavel P. |
collection | PubMed |
description | BACKGROUND: Recent Alzheimer’s disease (AD) genetics findings from genome-wide association studies (GWAS) span progressively larger and more diverse populations and outcomes. Currently, there is no up-to-date resource providing harmonized and searchable information on all AD genetic associations found by GWAS, nor linking the reported genetic variants and genes with functional and genomic annotations. OBJECTIVE: Create an integrated/harmonized, and literature-derived collection of population-specific AD genetic associations. METHODS: We developed the Alzheimer’s Disease Variant Portal (ADVP), an extensive collection of associations curated from >200 GWAS publications from Alzheimer’s Disease Genetics Consortium and other consortia. Genetic associations were systematically extracted, harmonized, and annotated from both the genome-wide significant and suggestive loci reported in these publications. To ensure consistent representation of AD genetic findings, all the extracted genetic association information was harmonized across specifically designed publication, variant, and association categories. RESULTS: ADVP V1.0 (February 2021) catalogs 6,990 associations related to disease-risk, expression quantitative traits, endophenotypes, or neuropathology. This extensive harmonization effort led to a catalog containing >900 loci, >1,800 variants, >80 cohorts, and 8 populations. Besides, ADVP provides investigators with a seamless integration of genomic and publicly available functional annotations across multiple databases per harmonized variant and gene records, thus facilitating further understanding and analyses of these genetics findings. CONCLUSION: ADVP is a valuable resource for investigators to quickly and systematically explore high-confidence AD genetic findings and provides insights into population-specific AD genetic architecture. ADVP is continually maintained and enhanced by NIAGADS and is freely accessible at https://advp.niagads.org. |
format | Online Article Text |
id | pubmed-9028687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-90286872022-05-06 Alzheimer’s Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer’s Disease Kuksa, Pavel P. Liu, Chia-Lun Fu, Wei Qu, Liming Zhao, Yi Katanic, Zivadin Clark, Kaylyn Kuzma, Amanda B. Ho, Pei-Chuan Tzeng, Kai-Teh Valladares, Otto Chou, Shin-Yi Naj, Adam C. Schellenberg, Gerard D. Wang, Li-San Leung, Yuk Yee J Alzheimers Dis Research Article BACKGROUND: Recent Alzheimer’s disease (AD) genetics findings from genome-wide association studies (GWAS) span progressively larger and more diverse populations and outcomes. Currently, there is no up-to-date resource providing harmonized and searchable information on all AD genetic associations found by GWAS, nor linking the reported genetic variants and genes with functional and genomic annotations. OBJECTIVE: Create an integrated/harmonized, and literature-derived collection of population-specific AD genetic associations. METHODS: We developed the Alzheimer’s Disease Variant Portal (ADVP), an extensive collection of associations curated from >200 GWAS publications from Alzheimer’s Disease Genetics Consortium and other consortia. Genetic associations were systematically extracted, harmonized, and annotated from both the genome-wide significant and suggestive loci reported in these publications. To ensure consistent representation of AD genetic findings, all the extracted genetic association information was harmonized across specifically designed publication, variant, and association categories. RESULTS: ADVP V1.0 (February 2021) catalogs 6,990 associations related to disease-risk, expression quantitative traits, endophenotypes, or neuropathology. This extensive harmonization effort led to a catalog containing >900 loci, >1,800 variants, >80 cohorts, and 8 populations. Besides, ADVP provides investigators with a seamless integration of genomic and publicly available functional annotations across multiple databases per harmonized variant and gene records, thus facilitating further understanding and analyses of these genetics findings. CONCLUSION: ADVP is a valuable resource for investigators to quickly and systematically explore high-confidence AD genetic findings and provides insights into population-specific AD genetic architecture. ADVP is continually maintained and enhanced by NIAGADS and is freely accessible at https://advp.niagads.org. IOS Press 2022-03-08 /pmc/articles/PMC9028687/ /pubmed/35068457 http://dx.doi.org/10.3233/JAD-215055 Text en © 2022 – The authors. Published by IOS 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 (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kuksa, Pavel P. Liu, Chia-Lun Fu, Wei Qu, Liming Zhao, Yi Katanic, Zivadin Clark, Kaylyn Kuzma, Amanda B. Ho, Pei-Chuan Tzeng, Kai-Teh Valladares, Otto Chou, Shin-Yi Naj, Adam C. Schellenberg, Gerard D. Wang, Li-San Leung, Yuk Yee Alzheimer’s Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer’s Disease |
title | Alzheimer’s Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer’s Disease |
title_full | Alzheimer’s Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer’s Disease |
title_fullStr | Alzheimer’s Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer’s Disease |
title_full_unstemmed | Alzheimer’s Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer’s Disease |
title_short | Alzheimer’s Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer’s Disease |
title_sort | alzheimer’s disease variant portal: a catalog of genetic findings for alzheimer’s disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9028687/ https://www.ncbi.nlm.nih.gov/pubmed/35068457 http://dx.doi.org/10.3233/JAD-215055 |
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