Analyze Variant Enrichment
in Real-time
in Real-time
1
SELECT cohort data from your machine, the cloud, or our project-hosting platform Mosaic 
2
ENTER a gene of interest 
3
IDENTIFY enriched genomic variants within the selected cohort 
4
HIGHLIGHT common variants in both the cohort and individual patient samples5
CLICK on a variant to view the most up-to-date annotations from ClinVar, VEP, gnomAD 
6
FILTER variants by enrichment, impact, and frequency
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VEP
Samtools
Tabix
vt
GNomAD
1000 Genomes
Phenolyzer
RefSeq
Gencode
HPO