Newborn genetic screening

Catalog of tests

CEN4GEN offers several innovative testing options for supplemental newborn screens, and these include:

CEN4GEN Rapid supplemental newborn screen: full multi gene sequencing panel

The CEN4GEN Rapid supplemental newborn screen: full multi gene sequencing panel is a cutting edge comprehensive screen which is clinically useful to detect and complement biochemical genetic findings in 100 genes which are associated with common genetic disorders that are treatable when detected early. The average turnaround time for results is as early as 1 to 2 days for full multi gene sequencing panel analysis.

Learn more about the CEN4GEN Rapid supplemental newborn genetic screen: full multi gene sequencing panel analysis

CEN4GEN Rapid supplemental newborn screen: full single gene sequencing analysis

The CEN4GEN Rapid supplemental newborn screen: full single gene sequencing panel is a cutting edge comprehensive screen which is clinically useful to detect and complement biochemical genetic findings in a single gene which is associated with a common genetic disorder that is treatable when detected early. The average turnaround time for results is as early as 1 to 2 days for full single gene sequencing analysis.

Learn more about the CEN4GEN Rapid supplemental newborn genetic screen: full single gene sequencing analysis

CEN4GEN supplemental newborn exome screen

The CEN4GEN supplemental newborn exome screen is a cutting edge comprehensive screen of more than 22000 genes. Especially clinically useful for screening a wide spectrum of genetic disorders which are treatable when detected early, to complement biochemical genetic testing. This test is also recommended and extremely informative for the clinical diagnosis of newborns with other clinical conditions which have a genetic basis, and for those newborns who are clinically symptomatic. Contact CEN4GEN for more information.

CEN4GEN supplemental newborn mitochondrial genome screen

The CEN4GEN supplemental newborn mitochondrial screen is a cutting edge comprehensive screen of the mitochondrial genome to complement biochemical genetic testing. This test is also extremely informative for the clinical diagnosis of newborns with other clinical conditions which have a genetic basis, and for those newborns who are clinically symptomatic. Contact CEN4GEN for more information.

CEN4GEN supplemental newborn whole genome screen

The CEN4GEN supplemental newborn genome screen; a cutting edge comprehensive screen of the whole genome. Especially clinically useful for screening a wide spectrum of genetic disorders which are treatable when detected early, to complement biochemical genetic testing. This test is also recommended and extremely informative for the clinical diagnosis of newborns with other clinical conditions which have a genetic basis, and for those newborns who are clinically symptomatic. Contact CEN4GEN for more information.