RNA-seq classification and reporting for hematologic malignancies.
Fusion detection, molecular subtype classification, lineage prediction, variant review, and automated clinical-style reporting.
Sample input
Sequencing files, metadata, panels, and reference assets for reproducible pipeline execution.
Analysis
Fusion, variant, expression, quantification, QC, and review workflows for hematologic malignancy cohorts.
Prediction
Lineage and subtype classifiers applied to expression-derived and variant-supported evidence.
Reporting
Structured outputs for interpretation, review, and clinical-style documentation.