| Primary biological target |
DNA from microorganisms in the analysed stool sample, according
to the test methodology.
|
Human genetic or genomic variants, depending on the test.
|
| Common sample |
Stool for gut microbiome profiling.
|
Often saliva or cheek swab for direct-to-consumer human genetic
testing; clinical tests can use other sample types.
|
| Typical question |
“What bacterial composition or microbiome-related patterns are
represented in this sample?”
|
“Which tested human genetic variants do I carry?” or a narrower
ancestry, trait, carrier or health-related question.
|
| Does the underlying information change? |
The gut microbiome can vary over time.
|
Germline variants inherited or established early in development
are generally stable, although not every genetic test is a germline test.
|
| Repeat testing |
A later stool sample can produce a different microbiome profile
because the microbial community and sample context may change.
|
Repeating the same germline variant test does not normally change
the inherited variant itself, although methods and scientific
interpretation can improve.
|
| Family implications |
The report concerns the microbial profile represented in the person's
submitted sample.
|
Inherited genetic information can have implications for biological
relatives because variants can be shared within families.
|
| Can it diagnose disease? |
A consumer microbiome report should not be treated as a stand-alone
medical diagnosis.
|
Some clinical genetic tests can contribute to diagnosis when properly
selected and interpreted; a generic consumer DNA test should not be
assumed to provide the same clinical function.
|
| Privacy focus |
Personal, sample, laboratory, report and account information deserve
careful review.
|
Human genomic information raises additional questions about inherited
information, biological relatives, reuse, research, sharing and retention.
|