Eureka Genomics' unique computational tools allows us to efficiently calculate the number of base changes necessary to "convert" each subsequence in the target (pathogen) genome to the closest subsequence present in the host/background genome(s). Thus, all the subsequences in the target (pathogen) genome that are present or close to the selected host/background genome(s) (e.g., human) are excluded from consideration and a small set of ultra-specific signatures is generated.

Genomics USA