Our Key Focus Areas
Somatic Variant Analysis (Cancer Genomics)
Detect mutations, CNVs, and structural variants in tumor samples. Differentiate driver vs passenger mutations. Support tumor-only and tumor–normal matched workflows.
Germline Variant Analysis
Identify inherited mutations linked to rare diseases, Mendelian disorders, and familial syndromes. Includes SNPs, indels, CNVs. Prioritization via clinical databases (ClinVar, OMIM, HGMD).
Pharmacogenomics (PGx) Analysis
Interpret variants affecting drug metabolism, efficacy, and toxicity. Generate actionable recommendations for personalized treatment.
Tumor Evolution & Clonality Analysis
Subclonal mutation detection to track tumor progression, relapse, or resistance. Support for liquid biopsy (ctDNA) and longitudinal monitoring.
Pathogen & Infectious Disease Genomics
Pathogen genome sequencing for outbreak tracking, resistance profiling. Metagenomic sequencing to detect unknown or mixed infections.
Multi-Omics Clinical Integration
Integrating genomic with transcriptomic or epigenomic data for deeper insights in cancer and rare diseases.