Unlock the full potential of the human genome with DrSeq, powered by Nucleome Informatics. Our advanced next-generation sequencing and expert bioinformatics deliver actionable insights for research, clinical discovery, and personalized medicine.
Our Services
Whole Genome Sequencing (WGS): Comprehensive analysis of coding and non-coding regions.
Exome Sequencing: High-resolution sequencing of protein-coding regions.
Pharmacogenomics & Precision Medicine: Arrays like PMD and PharmacoFocus guide therapy and rare disease insights.
Rare Disease & Reproductive Genomics: Identify causative variants in complex inherited conditions.
Eye Disorder Genomics: Specialized panels for inherited retinal disease genetics.
Genomic Testing Focus Areas
Oncology: Early detection, therapy selection, and monitoring using comprehensive genomic profiling.
Rare Diseases: Advanced panels to identify pathogenic variants in inherited disorders like DrSeq Inherited Retinal Disorders Panel.
Reproductive Health: Carrier screening, preconception, and prenatal genomic testing for informed reproductive decisions.
Neurological Disorders: Genetic testing to identify inherited and complex conditions, including depression, anxiety, and movement disorders. Panels include ataxias (Spinocerebellar, Friedrich’s, CANVAS), Huntington’s, Fragile-X, Myotonic Dystrophy, ALS/FTD, Kennedy’s disease, Oculopharyngeal muscular dystrophy, and Fuchs endothelial corneal dystrophy.
Cardiovascular Disorders: Precision testing for inherited and multifactorial conditions, including a Sudden Cardiac Death Genetic Panel to assess risk factors.
Why Choose DrSeq?
Cutting-edge Lab: Equipped with the latest sequencing technologies.
Expert Team: Scientists and bioinformaticians delivering reliable results.
Easy Access: Web-based test ordering and sample tracking.
Global Collaboration: Supporting research with high-quality genomic data.
Discover the future of genomics with DrSeq—where accuracy meets innovation.