GenDiseak
Empowering genomic data for interpretation and reporting
Profiling genomic data with monogenic and polygenic risk assessment at once
Extensive disease
risk assessment
TW23 analysis detects and annotates genetic variants for monogenic and polygenic disease risk assessment to support clinical decision.
Dynamic variant
analysis platform
TW23 analysis offers an streamlined NGS analysis and intuitive variant browsing interface with an interactive design and custom filtering settings.
State-of-the-art
variant classification
Our workflows classify variants according to the American College of Medical Genetics and Genomics (ACMG) guidelines and integrate over 80 public genomic databases.
AI-based genomic
evidence
TW23 team applies AI-based natural language processing (NLP) technology to mine over 32 million PubMed publications for prioritization and real-world evidence.
Services
