Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2022
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
_version_ 1784691682894151680
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
work_keys_str_mv AT kuksapavelp alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT liuchialun alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT fuwei alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT quliming alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT zhaoyi alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT kataniczivadin alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT clarkkaylyn alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT kuzmaamandab alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT hopeichuan alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT tzengkaiteh alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT valladaresotto alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT choushinyi alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT najadamc alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT schellenberggerardd alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT wanglisan alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease
AT leungyukyee alzheimersdiseasevariantportalacatalogofgeneticfindingsforalzheimersdisease