Project feedback
Request a Feature
Suggest a new DNA provider, trait, ancestry comparison, report improvement or technical capability.
The request backend is not connected yet, so this development page does not submit requests.
Request
Describe the feature
Useful requests explain what the user wants to learn or do, not only the implementation they imagine.
Useful requests
Examples
Requests can be scientific, technical or purely about making the report easier to understand.
MyHeritage, 23andMe, VCF, gVCF or whole-genome sequencing support.
Specific non-clinical traits with credible, genotype-specific evidence.
Historically interesting reference comparisons or better ways to explain population affinity.
Evidence sources, coverage checks or clearer handling of confirmation and uncertainty.
Navigation, accessibility, explanation modes or presentation improvements.
Criteria
How requests should be judged
Not every interesting idea belongs in a genetics report.
Scientific supportCan the claim be supported by credible evidence?+
New interpretations should have appropriate scientific provenance and enough information to produce genotype-specific wording rather than generic speculation.
CoverageCan the supported DNA inputs actually answer the question?+
A good feature may still need to wait for whole-genome or another input type if the current SNP array does not provide sufficient coverage.
Safety and interpretationCan it be presented without implying more certainty than the evidence supports?+
Clinical, pharmacogenomic and ancestry-related features need particularly careful wording and evidence gates.