The software hub developed by the Laboratory of Human Genetics of Infectious Diseases (HGID),
designed to facilitate and advance human genetics research from multiple dimensions.

Deep intronic variants
affecting recursive splicing

5'-UTR variants
impacting on translation

Intronic branchpoints variants
disrupting splicing

Intronic AG-gain variants
in between BP and acceptor site

Network-based heterogeneity clustering

Human gene connectome

Gene damage index

Mutation significance cutoff

Visualizing population genetics
and mutation deleteriousness

Extracting DNA / protein sequences for genetic variants

Genotyping CRISPR-Cas9-edited sequencing data

Integrating multi-batch cytometry datasets