Advanced analysis and visual analytics for Whole Genome Sequencing:

- Rapid analysis of raw DNA-seq reads to identify single nucleotide variants (SNVs), small indels and structural variants
Analysis available for single genome, trios, cohorts, or tumor-normal pairs
Industry standard tools published in peer-reviewed journals
Collaborate and share results across any extended research team



  • Intuitive results visualization with targeted charts and venn diagrams aligned with objectives
  • Annotated variant lists and interpretation