From individual gene panels to population-scale whole genome sequencing — choose the right solution for your research or clinical needs.
Complete 30x coverage of the human genome using Illumina NovaSeq 6000. Detect SNVs, indels, CNVs, and structural variants in a single assay.
Pre-designed and custom panels for oncology, cardiology, neurology, pharmacogenomics, and rare disease with >500x depth.
Bulk and single-cell RNA-seq for gene expression profiling, alternative splicing analysis, and novel transcript discovery.
Cloud-native analysis platform with AI variant interpretation, interactive genome browser, and automated clinical reporting.
CPIC-guided drug response profiling covering 100+ genes. Actionable reports for precision prescribing decisions.
AI-optimized gRNA design tool with off-target prediction, on-target scoring, and delivery format recommendations.
Every step of our pipeline is optimized for speed, accuracy, and clinical relevance.
Request a Demo48 hours from sample receipt to variant call for WGS. Industry-leading speed without compromising quality.
99.9% sensitivity and specificity for SNVs >5% allele frequency. Validated against GIAB reference standards.
Our ParaSeq™ AI classifies variants with 97% concordance to expert manual review, reducing interpretation time by 70%.
HIPAA-compliant infrastructure with end-to-end encryption. SOC 2 Type II certified. Your data stays yours.
Contact us for custom quotes on high-volume projects.
For academic and non-profit labs
For hospitals and diagnostic labs
For large-scale programs