Genetic test for detection of specific DNA sequences in plasma (qualitative probe-based assay)
This test checks for the presence of certain DNA fragments in your blood, often used to detect genetic mutations or specific biomarkers for research or diagnostic purposes.
["This test helps identify specific genetic material that may be linked to health conditions or research studies."]
Key facts at a glance
- LOINC
- 103177-2
- Short code
- ETEC DNA Wnd Ql NAA+probe
- Synonyms
- ETEC DNA Wnd Ql NAA+probe
- Category
- chemistry
- Sample
- serum
- Container
- Red-top tube (SST)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- probe-amp-tar
- Specimen volume
- 5 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
- Hemolysis max
- 500
- Lipemia max
- 1000
- Icterus max
- 500
- TAT
- 4–24 hours
- Order
- routine
What This Test Measures
The test analyzes a sample of your plasma to detect the presence of specific DNA sequences. These sequences may be associated with inherited conditions, cancer research, or other genetic studies. The method used involves a specialized probe to identify these sequences qualitatively, meaning it tells you whether the sequences are present or not, but not their exact quantity.
Why It Might Be Ordered
Your healthcare provider may order this test if you have a family history of certain genetic conditions, if you are participating in a clinical trial, or if research suggests your DNA could be relevant to a study. It’s also sometimes used in screening or research contexts to detect rare genetic markers.
Sample Collection and Preparation
A blood sample is drawn from your vein, and the plasma portion is separated for testing. The plasma is then processed and sent to a lab for analysis using the probe-based method. You may need to fast or avoid certain activities for a few hours before the test, depending on the specific instructions from your provider.
What to Expect After the Test
Results are typically qualitative, meaning you will receive a positive or negative result for the presence of the specific DNA sequences. Follow-up discussions with your healthcare provider will help interpret the results in the context of your health or research participation.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
◆Associated findings1
Short name
None
Frequently asked questions
How long will it take to get my results?
What does a positive result mean?
Is this test covered by insurance?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy