Our advanced genomic analysis platform enables comprehensive DNA sequencing, variant calling, and interpretation to identify genetic factors in diseases and treatment responses. Using cutting-edge bioinformatics tools and algorithms, we provide in-depth analysis of genomic data to support research, clinical diagnostics, and personalized medicine.
Comprehensive analysis of the complete genome to identify all genetic variations, including single nucleotide polymorphisms (SNPs), insertions, deletions, and structural variants.
Targeted analysis of protein-coding regions of the genome, providing a cost-effective approach to identify pathogenic variants in genetic disorders.
Advanced algorithms for variant classification, annotation, and pathogenicity prediction, incorporating multiple databases and computational approaches.
Our genomic analysis platform leverages state-of-the-art sequencing technologies and proprietary computational algorithms to provide accurate and comprehensive genomic insights:
Our genomic analysis solutions are designed to support a wide range of applications in research and clinical settings:
Identify genetic factors associated with increased risk for various diseases, enabling early intervention and preventive strategies.
Analyze genetic variants that affect drug metabolism and efficacy to guide personalized treatment decisions and reduce adverse effects.
Identify causal genetic variants in rare disorders, providing definitive diagnoses for patients with previously unexplained conditions.
Characterize somatic mutations in tumors to guide targeted therapies and monitor treatment response through liquid biopsies.
Contact our team to discuss how our genomic analysis platform can accelerate your research or clinical applications.
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