NAVIFY® Mutation Caller

Secondary Analysis Solution

NAVIFY Mutation Caller screen



  • Accurately and efficiently detect variants
  • DeepVariant for germline SNV/Indel calling
  • Somatic SNV/Indel and CNV calling as well as RNA fusion calling for KAPA HyperPETE
  • Turnkey solution that reduces turnaround time
  • Validated pipelines for KAPA reagents

NAVIFY Mutation Caller is for Research Use Only.
Not for use in diagnostic procedures.

NAVIFY Mutation Profiler is CE-IVD.