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
Deliverables:
- Intuitive results visualization with targeted charts and venn diagrams aligned with objectives
- Annotated variant lists and interpretation
