Medical software Congenica Prenatal™

clinicalgynecologyanalysis

Find the underlying genetic cause of fetal anomalies, faster For clinicians and researchers analyzing fetal anomalies , Congenica Prenatal is a pre-configured module available within the Congenica 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 challenges in prenatal diagnosis Prenatal diagnosis can help to inform decisions during pregnancy and after birth. However, 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 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 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 findings.