End-to-End Interpretation Platform
Full Suite of AI-Powered Tools
For Use in Both Clinical and Research Applications
Features:
| - Comprehensive Analysis for both FastQ and VCF Files | - Complete Annotation for Every Variant |
| - Automated Variant Classification | - RNA Transcriptome Analysis |
| - Real-time Literature Search | - 1-click Report Generation |
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To learn more about ENLITER and to schedule a live demonstration,
email info@BTGenomics
