Genomic DNA Identification Profile (Blood)
This test analyzes a sample of your blood to identify specific genetic material (DNA) for research or diagnostic purposes, often used in personalized medicine or disease research studies.
["This test helps identify genetic information from your blood sample for potential medical research or tailored treatment planning."]
Key facts at a glance
- LOINC
- 48010-3
- Short code
- Genechip ID Bld/T
- Synonyms
- Genechip ID Bld/T
- Category
- chemistry
- Sample
- whole-blood
- Container
- Lavender-top (EDTA)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- molgen
- Specimen volume
- 3 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h
- Hemolysis max
- 0
- Lipemia max
- 0
- Icterus max
- 0
- TAT
- 4–24 hours
- Order
- routine
What This Test Measures
The test detects and quantifies specific sequences of DNA present in your blood. It may involve analyzing whole blood or extracted genomic DNA to identify particular genetic markers, mutations, or sequences of interest for research or clinical applications.
How the Test Works
Blood is collected and processed to isolate DNA. Advanced techniques, such as microarray or sequencing methods, are used to identify and measure specific DNA fragments. This process may be part of a broader genomic study or targeted genetic analysis.
Common Uses
This test is often used in research settings to study genetic variations, identify biomarkers for diseases, or support personalized medicine initiatives. It may also be part of larger clinical trials or genetic screening programs.
Preparation
No special preparation is typically required for this test. You may be asked to fast or avoid certain medications depending on the specific study protocol, so it’s important to follow instructions provided by your healthcare provider or the research team.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Genomic DNA identification can provide insights into genetic predispositions, disease mechanisms, or responses to treatments. While this test is often exploratory or research-based, it may help inform future diagnostic or therapeutic approaches based on genetic findings.
Frequently asked questions
Will I need to do anything special before this test?
How long will it take to get my results?
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