Have confidence in large NGS panel research workflows

Streamline your research workflow with comprehensive patient-like controls with large NGS panels the Mimix™ reference standards range.

Benefit from:

  • Hundreds of variants covering hundreds of key cancer genes
  • Batch-specific VCF file to support your research aims
  • Cell line-derived controls, commutable to real patient samples

Available with multiple variant types, including structural and fusions blends, allowing you to:

  • Analyze genomic content as well as structural context
  • Access structural variants including Copy Number Variants (CNVs), translocations and large inserts/deletions (indels)
  • Use RNA fusions available in FFPE format

View the OncoSpan™ range for one of the world’s largest oncology reference standards.

For research use only. Not for use in diagnostic procedures.