MatchEngine V2
The MatchEngine is designed to match cancer patients to genomically driven, precision medicine clinical trials. While this version is a complete re-write from the ground up, it maintains feature parity and most default behaviors from the V1 MatchEngine, as well as integration with the MatchminerAPI (>=V1.0), and MatchminerUI (>=V1.0).
For documentation please see https://matchminer.gitbook.io/matchminer/
CHANGELOG:
- Add command line flag for matching to individual, or batches of trials
- Add command line flag for matching based on single sample IDs, or multiple IDs
- Add command line flag to output digraph visualizations of matching algorithm
- Adds support by default for new patient genomic criteria including tumor mutational burden, structural variations, and POLE, tobacco, temozolomide, and APOBEC signature statuses
- Allow for single or batch importing of JSON documents for all data types
- Introduce asynchronous query behavior
- Introduce plugin architecture for easy trial configuration/extensibility
- Trial matching criteria moved to extensible configuration files
- Fix bug related to reporting trial match reasons
- Fix sorting bug related to variant level match exclusions
- Fix bug related to matching on protein wildcard curations
- Add run_log to track additions, updates, and deletions to individual trials
- Expand documentation to include tutorials on getting started, trial curation, and engine configuration
- Add clinical reason(s) to trial match output documents