The UDN utilized CGAP’s customized rare disease variant callers to analyze thousands of whole genome samples and facilitate discovery across the UDN Cohort.
The UDN utilized CGAP’s customized rare disease variant callers to analyze thousands of whole genome samples and facilitate discovery across
the UDN Cohort.
The UDN utilized CGAP’s customized rare disease variant callers to analyze thousands of whole genome samples and facilitate discovery across
the UDN Cohort.
The PROACTIVE pilot project assessed CGAP’s performance and found that CGAP was able to successfully identify all actionable germ-line variants across all examined clinical cancer cases.
The PROACTIVE pilot project assessed CGAP’s performance and found that CGAP was able to successfully identify all actionable germ-line variants across all examined clinical cancer cases.
The PROACTIVE pilot project assessed CGAP’s performance and found that CGAP was able to successfully identify all actionable germ-line variants across all examined clinical cancer cases.