BioCode

The Intelligent Platform for Clinical Genomics

From patient intake to final report, BioCode provides a single, organized hub for all your data, ensuring clarity and traceability at every step.

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5

Clinical Assessment Modules

20+

Advanced Variant Filters

AI

Powered Interpretation

From Genome to Diagnosis, Faster

Manage

Centralize patient records, track analyses, and maintain complete audit trails.

  • ✓ Multi-tenant data isolation
  • ✓ Role-based access control
  • ✓ GDPR-compliant storage

Analyze

Accelerate your time to insight with powerful automated analysis tools.

  • ✓ 5 clinical assessment modules
  • ✓ 20+ variant filters
  • ✓ WES & WGS support

Report

Generate professional clinical reports with AI-powered summaries.

  • ✓ AI variant interpretation
  • ✓ Multi-language support
  • ✓ Secondary findings options

Specialized Clinical Assessments

Purpose-built diagnostic modules that automate complex clinical workflows and surface actionable findings.

Diagnosis

Phenotype-driven variant prioritization with categorized findings: Main, CNV, STR, Mitochondrial, and VUS.

Carrier Screening

Gene-based carrier status identification for recessive conditions with automated pathogenicity filtering.

BOC Assessment

Breast and ovarian cancer variant analysis with BRCA1/2 focus and hereditary risk evaluation.

Cancer Predisposition

Comprehensive hereditary cancer gene panel analysis for proactive risk management.

Explore all assessments →
AI-Powered

Intelligent Variant Interpretation

Generate clinical interpretations in seconds, not hours. Our AI analyzes prediction scores, population frequencies, OMIM annotations, and patient phenotypes to synthesize actionable insights.

  • ACMG criteria auto-applied with evidence trails
  • Multi-language report generation (English & Greek)
  • OMIM-based clinical summaries

AI Interpretation Engine

Cross-references ClinVar, OMIM, and patient phenotypes

WGS Premium

Advanced Whole Genome Sequencing Analysis

✓ CNV Analysis with IGV Browser
✓ HLA Typing
✓ SMN Gene (SMA Carrier)
✓ GBA Gene (Gaucher Risk)
Learn More About WGS Features

Introducing DONORmatch™

Our groundbreaking feature for intelligent donor selection. Optimize your IVF journey by ensuring the highest level of genetic compatibility.

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Secure & Compliant

GDPR Ready

Ready to Streamline Your Genomic Analysis Workflow?

See for yourself how BioCode can streamline your genomic analysis workflow.

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