Each frequency is matched against the genome database using sub-harmonic analysis. The results show which organisms have sequences whose nucleotide frequencies are harmonically close to your input.

Organism Summary starts with lowest deviation and the RRM scheme. You can change sort and scheme in that popup. Lift is a database-composition correction, not a clinical probability.

Saving is separate from Analyze — only archive runs you want to keep.

After analysis, use AI Insight to send the results to Google Gemini for interpretation in the context of a condition you specify.