Do not miss variants that matter in your NGS data.
The application of Whole Genome Sequencing within Human Genetics is steadily moving from research to clinic. The change to a clinical context demands consistent and predictable results whilst adhering to service levels and budget constraints in an operational environment with different urgency levels.
42Genetics ensures predictable service levels of 20 minutes per full genome processing to 1 hour for full genome trio analysis. Besides, our solutions allow highly sensitive variant calling for any number of custom selected essential clinical variants, assuring that no important variant will be missed.