| Autor: |
Kim, Jonggeol J., Makarious, Mary B., Bandres‐Ciga, Sara, Gibbs, Jesse Raphael, Ding, Jinhui, Hernandez, Dena G., Brooks, Janet, Grenn, Francis P., Iwaki, Hirotaka, Singleton, Andrew B., Nalls, Mike A., Blauwendraat, Cornelis |
| Zdroj: |
Movement Disorders; May2021, Vol. 36 Issue 5, p1250-1258, 9p |
| Abstrakt: |
Background: Parkinson's disease (PD) is a genetically complex neurodegenerative disease with ~20 genes known to contain mutations that cause PD or atypical parkinsonism. Large‐scale next‐generation sequencing projects have revolutionized genomics research. Applying these data to PD, many genes have been reported to contain putative disease‐causing mutations. In most instances, however, the results remain quite limited and rather preliminary. Our aim was to assist researchers on their search for PD‐risk genes and variant candidates with an easily accessible and open summary‐level genomic data browser for the PD research community. Methods: Sequencing and imputed genotype data were obtained from multiple sources and harmonized and aggregated. Results: In total we included a total of 102,127 participants, including 28,453 PD cases, 1650 proxy cases, and 72,024 controls. Conclusions: We present here the Parkinson's Disease Sequencing Browser: a Shiny‐based web application that presents comprehensive summary‐level frequency data from multiple large‐scale genotyping and sequencing projects https://pdgenetics.shinyapps.io/VariantBrowser/. Published © 2021 This article is a U.S. Government work and is in the public domain in the USA. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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