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DNA Labs India

Torch DNA Detection Test

DNA Labs India | ISO 9001:2015 Certified

Torch DNA Detection Test

Short Name: TORCH DNA Test

Also known as: TORCH Infection Panel, TORCH DNA PCR, TORCH Detection Test

Torch DNA Detection Test test available at DNA Labs India for ₹10,500. Uses Polymerase Chain Reaction (PCR) on Plasma / CSF / Amniotic fluid samples. Results in Reports are delivered within 8 days of sample receipt. You will receive a notification on your registered mobile number and email.. Free home collection in 300+ cities across India.

PCRFemaleAdult🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the TORCH DNA Detection Test is to directly detect the presence of DNA from Toxoplasma gondii, Rubella virus, Cytomegalovirus, and Herpes simplex virus in clinical samples. This aids in the diagnosis of active or recent infections, especially in pregnant women, to assess the risk of vertical transmission and guide clinical management.

Test Code
3704
Price
₹10,500
Sample Type
Plasma / CSF / Amniotic fluid
Result Time
Reports are delivered within 8 days of sample receipt. You will receive a notification on your registered mobile number and email.
Fasting Required
No
Method
Polymerase Chain Reaction (PCR)
Step 1

Sample Collection

No special preparation is required before the test. Please inform your doctor about any medications or supplements you are taking. For amniotic fluid or CSF collection, the procedure will be explained in detail by your healthcare provider.

Method: Venipuncture / Healthcare provider collection

Step 2

Laboratory Analysis

A blood sample will be collected from a vein in your arm by a trained phlebotomist. If CSF or amniotic fluid is needed, the sample will be collected by a qualified specialist under strict sterile conditions.

Step 3

Report Delivery

After a blood draw, apply gentle pressure at the puncture site and keep it covered for a few minutes. You may resume your normal activities immediately. If you had a CSF or amniotic fluid collection, your healthcare provider will provide specific aftercare instructions.

Timeline: Reports are delivered within 8 days of sample receipt. You will receive a notification on your registered mobile number and email.

Patient Instructions

1
Before the Test:No special preparation is required. You may eat and drink normally. Inform your doctor about any medications or underlying conditions like bleeding disorders.
2
During the Test:For blood collection, a tourniquet is applied and a needle is inserted into a vein in your arm. The procedure takes less than a minute. For CSF/amniotic fluid, a specialist performs the collection using a sterile technique.
3
After the Test:You can leave immediately after the test. If you had a blood draw, keep the bandage on for a few hours. Contact your doctor if you experience unusual pain, swelling, or bleeding at the puncture site.

About This Test

Who Should Get This Test

The purpose of the TORCH DNA Detection Test is to directly detect the presence of DNA from Toxoplasma gondii, Rubella virus, Cytomegalovirus, and Herpes simplex virus in clinical samples. This aids in the diagnosis of active or recent infections, especially in pregnant women, to assess the risk of vertical transmission and guide clinical management.

How to Prepare

  • Wear comfortable clothing with sleeves that can be rolled up
  • Bring your prescription or test requisition form
  • Inform the phlebotomist if you have a bleeding disorder or are on anticoagulant therapy
  • For CSF or amniotic fluid collection, no special preparation is needed
  • The sample must be transported refrigerated and should not be frozen

Doctor's Notes

Reviewed by — MBBS, MD (Microbiology) · Reg. No. 27670

"The TORCH DNA PCR test provides direct evidence of infection, which is crucial for determining the risk of vertical transmission during pregnancy. Early identification enables prompt management and better outcomes for both mother and baby."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypePlasma / CSF / Amniotic fluid
Sample Volume4 mL (2 mL min.) plasma OR 3 mL (2 mL min.) CSF/Amniotic fluid
ContainerLavender top (EDTA) tube OR sterile screw capped container
Collection MethodVenipuncture / Healthcare provider collection

Sample Stability

Room TemperatureNot Acceptable (NA)
Refrigerator (2-8°C)72 hours
Frozen (-20°C or below)Not Acceptable (NA)
Sample Rejection Criteria:
  • Clotted or hemolyzed sample
  • Sample received at wrong temperature (frozen or excessive heat)
  • Improper labeling or missing patient identifiers
  • Sample not transported in sterile container
  • Request form incomplete

Understanding Your Results

The TORCH DNA Detection Test yields qualitative results: 'Detected' or 'Not Detected' for each pathogen. Detection of DNA indicates the presence of the organism in the clinical sample, which may suggest active infection or significant viral/bacterial presence. Correlation with clinical presentation and serological markers is essential for accurate interpretation.
📊

Positive

Indicates active toxoplasmosis or recent infection. In pregnancy, further risk assessment and treatment are required.

📊

Negative

No Toxoplasma DNA detected. If clinical suspicion remains, repeat testing or serology may be considered.

📊

Positive

Suggests rubella virus infection. In pregnancy, this is associated with congenital rubella syndrome; urgent specialist consultation is essential.

📊

Negative

No Rubella virus DNA detected, making active rubella unlikely.

📊

Positive

Indicates CMV infection or reactivation. May be transmitted to fetus in pregnancy; monitoring and antiviral therapy may be considered.

📊

Positive

Suggests active HSV infection, which may pose risk during delivery. Discuss with your doctor regarding delivery planning and antiviral treatment.

⚠️ When to Consult a Doctor:

If you are pregnant and have symptoms such as persistent fever, rash, lymph node swelling, or flu-like illness, or if you have been exposed to a TORCH infection, speak with your obstetrician or infectious disease specialist promptly. Early detection and management can help prevent congenital complications.

Limitations

  • Detects only the four listed pathogens; other infectious causes are not covered
  • A negative result does not entirely rule out infection, especially if sampled during the very early incubation period
  • Results should be correlated with clinical findings and serological tests for comprehensive diagnosis
  • Quantitative viral load is not provided by this qualitative test

Risks & Considerations

  • Bruising or mild pain at the needle site
  • Small risk of infection at the puncture site
  • Dizziness or fainting during blood collection
  • For CSF or amniotic fluid: risk of bleeding, infection, or injury (rare, performed only when clinically indicated)

Interfering Factors

  • Insufficient sample volume
  • Improper sample storage at room temperature for extended periods
  • Hemolysis or clotting of the blood sample
  • Presence of PCR inhibitors in the sample
  • Contamination during sample collection or processing

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Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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