Output Catalog
ASAP is committed to accelerating the pace of discovery and informing a path to a cure for Parkinson’s disease through collaboration, research-enabling resources, and data sharing. We’ve created this catalog to showcase the research outputs and tools developed by ASAP-funded programs.
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ASAP CRN Cloud Release Notes – Version 2.0.0
Version: 2.0.0 Release Date: December 11, 2024 This release notes document provides a concise overview of the updates and enhancements introduced in Version 2.0.0 of the CRN Cloud platform.
ASAP CRN Cloud Release Notes – Version 1.0.0
Version: 1.0.0 Release Date: June 25, 2024 This release notes document provides a concise overview of the updates and enhancements introduced in Version 1.0.0 of the CRN Cloud platform.
ASAP CRN Cloud Release Notes – Version 1.0.0-beta
Version: 1.0.0-beta Release Date: March 6, 2024 This release notes document provides a concise overview of the updates and enhancements introduced in Version 1.0.0-beta of the CRN Cloud platform.
ASAP CRN Cloud Release Notes – Version 0.0.1
Version: 0.0.1 Release Date: November 10, 2023 This release notes document provides a concise overview of Version 0.0.1 of the CRN Cloud platform.
Release Notes – ASAP CRN Cloud
Summary: Release notes for version 3.0.0 of CRN Cloud platform, released on September 30, 2025, detailing latest updates and enhancements.
Time to LiD GWAS dataset
Code to perform the study of LiD genetic determinants under CPH regression models and functional annotation analyses
Genome-wide determinants of mortality and clinical progression in Parkinson’s disease – Summary statistics
Summary statistics from "Genome-wide determinants of mortality and clinical progression in Parkinson’s disease."
QSBB Digital Pathology Resource
This digital pathology resource contains digital whole slide images from Lewy body disorders: Parkinson’s disease, Parkinson’s disease with dementia, dementia with Lewy bodies, and control cases.
Targeted long-read RNA-seq
Targeted long-read RNAseq of SNCA, GBA1, and GBAP1. Three datasets are available: (i) human brain (ii) iPSC-derived astrocytes microglia neurons and (iii) iPSC-derived midbrain dopaminergic neurons.
Dataset: Parkinson’s Families Project: a UK-wide study of early onset and familial Parkinson’s disease
Parkinson’s Families Project, aims to identify genetic variations linked to familial and early-onset Parkinson's disease. SNP array genotyping, MLPA, and WGS were performed to study pathogenic mutations and their association with clinical factors.
SNP Array Genotyping and Phenotypic Data: “Parkinson’s Families Project: a UK-wide study of early onset and familial Parkinson’s disease”
Study on Parkinson's disease families in the UK collected genotypic data from 698 samples using Illumina NeuroChip SNP Array and phenotypic data from 718 samples. The datasets are publicly accessible via EGA.
Cleaned datasets used to perform statistical analyses: “Parkinson’s Families Project: a UK-wide study of early onset and familial Parkinson’s disease”
Study on early onset Parkinson's disease used a pseudo-anonymised dataset for statistical analyses. Clean data was used to analyze polygenic risk scores and principal components in two models.
