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Congenica Prenatal

Time is of the essence

Rapidly identifying genetic causes of fetal anomalies is crucial to provide timely personalised treatments for both, mother and baby, before and after birth. However, not only is the knowledge of fetal genotype/phenotype correlation limited, but around two-thirds of single gene disorders resulting in an abnormal ultrasound arise de novo.

Prenatal Analysis with Congenica

Prenatal Analysis with Congenica Prenatal Exome Congenica

 

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Prenatal Analysis with Genomic Medicine

Prenatal Analysis with Congenica Prenatal Exome Congenica (1)

 

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Overcoming the challenges in prenatal analysis

We have developed Congenica Prenatal, a pre-configured and expertly curated analysis module within the Congenica Platform, that allows you to rapidly identify genetic causes in fetuses with abnormal ultrasound to ensure life-changing interventions can be considered effectively.
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Rapid turnaround time

Expertly curated and annotated preconfigured virtual gene panels with prenatal phenotype-specific PubMed identifiers, coupled with instant preconfigured reporting to accelerate analysis and interpretation

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High flexibility

Highly flexible platform with customisable reporting for whole genome, exome or gene panel analysis and variant interpretation

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Evidence-based

Accurate variant interpretation based on highly curated variant lists specific for prenatal analysis and prioritised for pathogenicity (ClinGen, ClinVar, Genomics England PanelApp, literature review, and other trusted sources)

Congenica Prenatal enables fast, accurate and evidence-based interpretation of prenatal variants to reduce the critical time from sample to report

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Deciphering Developmental Disorders

Copy of Deciphering Developmental Disorders (4)

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See what our customers say about Congenica

READ OUR CUSTOMER TESTIMONIALS