Mutant now offers two DNA-based ways to begin:
Both use your DNA together with your questionnaire context to organize patterns into the communities and hubs most relevant to you.
The difference is not whether DNA is included.
The difference is how much of the genome is visible, how complete the biological picture can be, and how much confidence you can place in deeper or narrower pathways.
| Feature | Starter | WGS |
|---|---|---|
| DNA source | 23andMe / AncestryDNA microarray raw data | Whole-genome sequencing |
| Coverage depth | Partial | Broadest and deepest |
| Best for | Fastest entry into Mutant with common consumer DNA files | People who want the most complete genomic view |
| What you get | Hub-based analysis, ranked drivers, and protocol exploration from the portion of the genome your file captures | Deeper driver resolution, broader biology coverage, and stronger visibility into narrower or less-covered pathways |
| Good fit if you are asking... | "Can Mutant help me make sense of this pattern?" | "What is the fullest version of my picture?" |
| Can you upgrade later? | Yes | Already includes the deepest version |
Starter is Mutant's microarray-based entry point.
It works with common raw DNA files from 23andMe and AncestryDNA and is built for people who want to begin now without needing whole-genome sequencing first.
Starter can still help you:
Starter is meant to be useful on its own.
It is not just a placeholder.
But it is also not the fullest genomic view.
Starter uses microarray DNA, which only captures a subset of the genome.
That means some pathways may come through clearly, while others may be only partly visible or not visible enough to resolve with confidence.
This matters most in narrower or deeper areas such as:
So if you use Starter, you may still get a meaningful direction — but not the complete picture.
A good way to think about it is:
Starter can help you begin in the right community and explore relevant protocol tracks. WGS is what you choose when you want broader genomic visibility and fewer blind spots.
WGS is Mutant's full-depth option.
It is the better fit when you want the broadest possible coverage across the pathways Mutant models, especially when your questions depend on biology that consumer microarray files often miss or only partly capture.
WGS is best if you want:
For users focused on oxalates, histamine, sulfur, methylation, supplement sensitivity, or layered reactivity, WGS will often provide the more complete foundation.
Starter is usually the best fit if:
Starter is especially useful as a first pass.
It helps you get oriented, see what is already visible, and decide whether upgrading to WGS is worth it for your case.
WGS is usually the better fit if:
These are not competing products.
They are two ways to enter the same Mutant framework.
Many people begin with the DNA file they already have.
Starter lets you:
If the picture still feels incomplete — or if the biology you care about is only partly covered — you can go deeper later.
That is often the right move when:
Starter uses common consumer DNA files from 23andMe and AncestryDNA. These files can still be useful, but they do not capture the full genome. Some hubs and protocol tracks may come through clearly, while others — especially in areas like oxalates, histamine, sulfur, and methylation — may only be partly visible. Starter is best viewed as a partial genomic map with real value now, not a full-resolution picture.
Yes. Starter uses 23andMe or AncestryDNA raw DNA files.
Yes. Starter is designed to be useful on its own and can help you find the right hub, see supported drivers, and explore protocol directions.
WGS gives broader genomic coverage and a more complete view of pathways that microarray files may miss or only partly capture.
Yes, sometimes. That is the tradeoff. Starter can still be useful, but it gives a partial view of the biology.
Yes. Starter can still help you explore protocol paths and community roadmaps. The difference is that some of those paths may be supported more partially than they would be under WGS.
Yes. You can begin with Starter and upgrade later if you want deeper coverage.
Choose Starter if you already have 23andMe or AncestryDNA and want to begin now with a lower-cost, partial genomic view.
Choose WGS if you want the broadest coverage and the deepest version of your Mutant analysis from the start.
Mutant provides educational, informational analysis and is not a substitute for medical advice, diagnosis, or treatment.