In the fight against disease, our NGS solutions provide the valuable insights needed to advance non-clinical healthcare research. From sequencing a few genes, to the whole exome, to the whole genome, Rapid Genomics provides total NGS solutions focused on high-quality, cost-effective data.
WGS scans the entire genome for the comprehensive discovery of genetic mutations, structural variants, and copy number variants with a single assay. Rapid Genomics can adjust the sequencing depth to meet research goals and project requirements.
Any sample volume
Tunable sequencing depth
Flexible data reporting
Custom data analysis
Exome sequencing provides efficient, targeted sequencing results to investigate disease, rare disorders, cancer, or population studies. Capture-Seq is more cost-effective than WGS in targeting protein coding regions, without limiting detection range of rare variants.
Any sample volume
Tunable sequencing depth
Multiple exome panels available
Custom data analysis