Unlock knowledge at the molecular level

MH Guide makes interpreting and reporting of clinical variants faster, easier and more accurate. It contextualizes patient-specific molecular data against global biomolecular knowledge and does it faster than you would imagine. In fact, clinical annotation and molecular data processing that used to take days now takes minutes. MH Guide 2.3 contains:

• Interpretation of combination biomarkers

• The option of reporting wildtype Clinical Variant Interpretations (CVIs)

• A new CVI-centric view

• Summary statistics on mutational load

• Encryption of PHI data

• The option of including an electronic signature in a signed report

• Filtering based on the maximum population frequency across all ethnicities