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.
"Alamut is the best tool I have used for the annotation of DNA variants. It has a great user interface, combines data from multiple sources and allows for ease of variant interpretation by clinical geneticists."
JORDAN LERNER-ELLIS, Ph.D.
Mt. Sinai Hospital, Toronto