Profiling genomic data with monogenic and polygenic risk assessment at once
Extensive diseaserisk assessment
TW23 analysis detects and annotates genetic variants for monogenic and polygenic disease risk assessment to support clinical decision.
Dynamic variantanalysis platform
TW23 analysis offers an streamlined NGS analysis and intuitive variant browsing interface with an interactive design and custom filtering settings.
State-of-the-artvariant 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 genomicevidence
TW23 team applies AI-based natural language processing (NLP) technology to mine over 32 million PubMed publications for prioritization and real-world evidence.
Services
