Learn about the current and future initiatives of the International Collaboration for Clinical Genomics (ICCG)! As part of our commitment to data sharing and collaboration to improve patient care, ICCG is creating a universal, clinical-grade database of genomic variation (including structural and sequence variants), available to the public through resources such as NCBI’s ClinVar database, and much more.
"We were early Alamut adopters and this software has become essential to our daily diagnosis lab practice, saving time and reducing mistakes. The intuitivity of use and the new functionalities are a very useful help in our daily work."
PASCALE RICHARD M.D. Ph.D.