May 29, 2026
Introducing a new option: CentoScreen Exome
Designed for low-risk couples with no known family history of genetic disorders, CentoScreen Exome provides physicians and couples with a simple and comprehensive genetic screening solution.
Providing couples and physicians with a simple screening genetic test designed for unaffected couples with no known family history of genetic disorders.
Deep Dive in CentoScreen Portfolio:
NEW: CentoScreen Exome
Offering 3 variant based analysis:
- CentoScreen Exome Focused with More than 13,900 variants in 141 genes(Solo/Duo)
- CentoScreen Exome Focused Plus with More than 36,000 variants in 539 genes(Solo/Duo)
- CentoScreen Exome with More than 55,000 variants in 1907 genes (Solo/Duo)
- Designed for Low Risk Couples
CentoScreen Genome
- Accurate Variant Screening (more than 60,000 variants** in 1921 genes)
- Fast TAT (15 business days)
- Designed for Low Risk Couples
CentoScreen Genome Comprehensive
- Expanded Carrier Screening (covering more than 2,000 genes associated with autosomal recessive and x-linked early-onset disorders)
- Complex variant detection using specific pipelines for AR, CYP21A2, GBA1, HBA, FMR1, FXN, CSTB, SMN1
- Improved Diagnostic Yield
- Designed for High Risk Couples
Our reproductive genetic carrier screening panels assess the risk of passing genetic variants to offspring, supporting informed family planning and peace of mind for couples.
The Earliest Step to Responsible Family Planning
