Fast and Accurate NGS Analysis at an Affordable Price with SEQ by Genomize 


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Thank you !

Thank you very much to our 307 users from 230 different hospitals/labs in 14 countries for processing 150,000+ samples.

Genotype Phenotype Database
You can build your real-time genotype / phenotype database


Extended Annotation by Genomize
Do not miss any pathogenic variant by checking all available transcripts with ACMG standards

Clinical Diagnosis Report
The customizable clinical diagnosis report feature saves lots of time


Clinical Somatic Analysis
Classify variants as drug sensitive, resistant, prognostic, and diagnostic, overlay with clinical trials

Accurate Pipelines
Small variation and CNV detection with gold standard bioinformatics algorithms

Filter variants 80% more effectively
Use SEQ to build an allele frequency pool and filter regional polymorphisms out