Torres Quevedo Programme 2013. MINECO
After many developments based on array CGH technology, NIMGenetics takes a technological leap, implementing massive sequencing. This project represents the development of ExoNIM®, a complete exome sequencing platform for the genetic diagnosis of neuropediatric diseases, especially focused on identifying the genetic causes of syndromic and non-syndromic intellectual disability. NIMGenetics complements its portfolio of services with the development of diagnostic platforms based on sequencing, becoming an integrated centre that uses the latest technologies for comprehensive molecular diagnosis.