Find the underlying genetic cause of fetal anomalies, faster
For healthcare professionals analyzing fetal anomalies, Congenica Prenatal is a pre-configured application available within Congenica’s clinical decision support platform, with expertly curated and annotated gene panels, enabling you to identify the genetic causes of ultrasound-detected fetal anomalies faster than ever before.
Overcoming the challenge of prenatal diagnosis
Prenatal genetic diagnosis is a critical but complex clinical challenge to inform decisions during pregnancy and after birth. Knowledge of fetal phenotypes is limited with most gene phenotype data from postnatal cases. Around two-thirds of single gene causes of anomalies arise de novo.
Congenica Prenatal has been expertly curated to provide clinical teams with the evidence and expertise to overcome these challenges and analyze cases faster, with confidence to provide a rapid response.
Perform complete prenatal analysis in a single solution
Congenica Prenatal provides flexibility and optimization across your clinical workflow. Upload whole genome, exome or gene panel data, annotate and interpret variants, and generate your report all in one place. Then present your findings using report templates specifically designed to support prenatal genomic medicine.
Fast, accurate and evidence-based
Congenica Prenatal enables fast, accurate and evidence-based interpretation of variants in the prenatal setting to decrease the time from sample to review and provide a rapid response. The application includes hundreds of genes and variant lists curated and prioritized for pathogenicity from ClinGen, ClinVar, Genomics England PanelApp, literature review, and other trusted sources to support analysis and molecular diagnosis of fetal anomalies.
Our team of experts has curated and annotated preconfigured gene panels with PubMed identifiers signposting you to prenatal phenotype relevant literature for over 190 genes, simplifying clinical workflows.
Time-saving and life-changing
In prenatal diagnosis every minute matters. Our literature annotations and instantly generated prenatal reports will help you save a further 45-minutes in the interpretation and reporting of fetal anomalies per case in addition to the hours that the Congenica platform already saves in post-natal cases.
Identifying the precise molecular cause of a fetal abnormality using exome sequencing is a major step forward. In addition to allowing parents to make informed decisions about pregnancy and birth, it is an essential step in developing early interventions using the treatments now available both in utero and in early postnatal life.
See how Congenica Prenatal can increase your diagnostic yield, confidence and efficiency