Next-Generation Genomic Interpretation
Chimera is a tertiary analysis system fully integrated with Phoenix and Empyrica.
Using Chimera, one can quickly identify variants of interest, mark them for clinical reporting and/or research purpose, generate reports and export data for further research.
For diagnosis of Mendelian disorders, Chimera can discover relevant pathogenic variants quickly using its proprietary machine learning-based ranking algo to prioritize candidate genes using phenotypes as input.
Feature highlight
- Fast Annotation (WES samples takes only seconds to complete)
- Broad set of reference databases, periodically updated
- Algo guided filtering / Phenotype-driven candidate gene prioritization
- Integrated alignments (BAM) viewing
- Presets for optimized workflow
- Reporting and report templates
- Curatable, searchable results for clinical review and research (marking, scoring, commenting)
