MDGP
v0.1 beta

MDGP
Movement Disorders Genome Program

A multi-center initiative integrating whole-exome, whole-genome, and long-read sequencing with epigenomic and metabolomic profiling across PD, ET, and matched controls in China.

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A Population-Scale Multi-Omics Resource

Harmonized clinical and multi-omics data from the MDGP consortium, spanning whole-exome, whole-genome, long-read sequencing, WGBS, and metabolomics.

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Total Participants
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PD Cases
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ET Cases
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Controls

Cohort Demographics & Data Distribution

Population stratification and sample distribution across geographic regions, age groups, and gender.

Regional Distribution

Age Distribution (n=14,383)

Gender Ratio by Cohort

Integrated Genomic Analysis

Explore and analyze movement disorders genomic data through a unified portal.

Genome Browser

Interactive visualization of genomic variants and coverage tracks across all chromosomes.

Haplogroup Explorer

Browse mtDNA and Y-chromosome haplogroup distributions with phylogenetic trees.

Coming Soon

GWAS Catalog

Search genome-wide association results for 48+ phenotypes with Manhattan plots.

Coming Soon

Collaborating Institutions

Research organizations and universities contributing to the MDGP.

Partner Organizations