Long and short read compatible variant calling files for comprehensive variant insights based on ACMG and AMP guidelines.

Somatic variant AMP tiering, with oncogenicity and pharmacogenomic insights.

Identify de novo mutations and perform carrier screening with high accuracy.

Complete tumor profiling with somatic mutation burden, mutation signature, and clonal complexity analysis

The platform provides pharmacogenomic insights for germline and somatic variants, derived from FDA-approved drugs and the latest research. It also includes an active clinical trials database to help identify various patient treatment options.

AI-powered agent to connect phenotype data with genomic variants, and prompt based pathogenic variant insights.

The platform integrates gene-level expression with single-cell (SC) transcriptomics and proteomics. It provides a comprehensive collection of single-cell atlases and supports the upload of patient-derived SC datasets

Generate automated clinical-grade reports with customizable templates.

Over 20x speedup compared to traditional tertiary analysis pipeline, including multi-omics integration.