| Home > Publications Database > The Global Parkinson's Disease Genetics (GP2) Genome Browser. |
| Journal Article | DZNE-2026-01005 |
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2026
Wiley
New York, NY
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Please use a persistent id in citations: doi:10.1002/mds.70309
Abstract: Large-scale sequencing initiatives have generated extensive genomic resources essential for variant interpretation, yet their effective use often requires bioinformatics expertise. To support identification of Parkinson's disease (PD) risk and disease-causing variants, we developed an open-access, summary-level genomic data browser.We performed uniform joint variant calling to harmonize whole-genome sequencing (WGS) data from AMP-PD Release 4, GP2 Data Releases, and additional controls from the Alzheimer's Disease Sequencing Project. Clinical-exome sequencing (CES) data from GP2 Release 8 were also included.The integrated dataset included 31,665 WGS and 9,559 CES samples, spanning 11 ancestries and over 300 million variants.The GP2 Genome Browser is a lightweight, flexible platform providing intuitive gene- and variant-level summaries with ancestry-stratified allele frequencies and functional annotations. It is open source and freely accessible at https://gp2.broadinstitute.org, enabling broad access to PD genomic data and supporting global research efforts. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
Keyword(s): Humans (MeSH) ; Parkinson Disease: genetics (MeSH) ; Whole Genome Sequencing (MeSH) ; Genetic Predisposition to Disease: genetics (MeSH) ; Databases, Genetic (MeSH) ; Genomics (MeSH) ; Web Browser (MeSH) ; Exome Sequencing (MeSH) ; Parkinson's disease ; browser ; genetics ; sequencing
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