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

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