Your platform. Now expanded.
Discover next-generation genomics.
A decade of rare disease excellence, now expanding into oncology and infectious disease with clinical-grade precision.
Pinpoint clinically relevant variants in seconds. Filter, prioritize, and act with confidence.
See exactly where your sequencing hits and where it doesn't, so nothing gets missed.
Visualize patient data in full genomic context, right alongside your annotations and tracks.
Surface the research that matters most, automatically matched to your variants and genes.
GermVar Pipeline
One pipeline for Panels, WES & WGS. Multi-caller architecture with haplotype-based calling, CNV & SV detection, mitochondrial analysis, mosaic detection, and built-in STR expansion.
GenomeAlert Re-Analysis
Never miss a diagnosis. Automatically re-analyse unsolved cases against updated databases each month and alerts you when new evidence could change a patient's outcome.
Flexible Filtering
Comprehensive filter engine for SNV/Indels and CNV/SVs. Combine presets with Preset Combos, mark favorites, and share configurations across your entity or keep them private.
DiagAI Autofill
Generate clinical-scientist-level variant comments with a single click. Near report-ready narratives in seconds, drastically cutting manual writing time.
ACMG Automation
Best-in-class ACMG criterion automation with ClinGen guidelines and gene-specific VCEP recommendations. Classifications follow the latest expert-curated rules out of the box.
DiagAI Prioritization
Identify disease-causing variants with full transparency. UP² score breakdown via waterfall plots, phenotypic matching, and clear explanations of every ranking — so you understand every recommendation.
Identify acquired mutations in cancers.
Pinpoint germline variants.
Detect microbial pathogens.
Your data stays yours—never shared, never sold. Our patented double-encryption system secures each patient file with a unique key for maximum data protection. You stay safe, compliant, and in control.
SeqOne Platform is a Class C, CE-IVDR certified in vitro diagnostic medical device, manufactured by SeqOne SAS (France). In the United Kingdom, SeqOne Platform is distributed under the Congenica brand by Congenica Ltd, a UK affiliate of SeqOne SAS. Congenica Ltd acts as the UK Responsible Person in accordance with UK MDR 2002.The company is certified under ISO 13485 for medical device manufacturer, and under ISO 27001 for information security and health data hosting.
With 92% specificity, SmartPick instantly suggests the most likely disease-causing variants
*Study on singleton with HPOs
Achieve diagnosis in record time with 90% of causal variants ranked in the top 3.
Validate Congenica with your own data, expert support, and zero commitment.
Pay-per-analysis with no hidden fees or volume constraints.
Access field specialists, multi-lingual assistance and hands-on guidance.
