CentoIEM NGS Genetic Test
Short Name: CentoIEM
Also known as: CentoIEM NGS, Inherited Metabolic Disorders NGS Panel
CentoIEM NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in Reports are typically available 3 to 4 weeks after the sample is received at the laboratory.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
The purpose of this test is to identify genetic mutations responsible for inherited metabolic disorders (IMDs), allowing accurate diagnosis, management, and genetic counselling.
- Test Code
- 3846
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- Reports are typically available 3 to 4 weeks after the sample is received at the laboratory.
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No special preparation or fasting is required. However, a genetic counselling session is required before the test to obtain family history and draw a pedigree chart.
Method: Venipuncture or FTA card blood spot
Laboratory Analysis
A small blood sample will be collected by a trained phlebotomist. For FTA card, a drop of blood from a fingertip is applied to the card.
Report Delivery
You may resume normal diet and activities. The sample will be transported to the laboratory at ambient temperature.
Timeline: Reports are typically available 3 to 4 weeks after the sample is received at the laboratory.
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this test is to identify genetic mutations responsible for inherited metabolic disorders (IMDs), allowing accurate diagnosis, management, and genetic counselling.
How to Prepare
- Do not put anything on the FTA card except blood
- Label the samples clearly
- Avoid haemolysis
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"For patients with suspected inherited metabolic disorders, genetic testing supports confirmation of diagnosis, genetic counselling, and informed family planning decisions. It is especially relevant in consanguineous families or previous history of unexplained neonatal deaths."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Haemolysed blood sample
- Insufficient DNA quantity
- Mislabeled sample
Understanding Your Results
Pathogenic variant detected
Confirms molecular diagnosis of an inherited metabolic disorder.
No pathogenic variant detected
No disease-causing variant found; clinical correlation is still necessary.
Variant of unknown significance
More research/family testing needed to determine clinical significance.
If you or your child experiences symptoms such as unexplained seizures, developmental regression, poor feeding, or metabolic crises, consult a clinical geneticist or pediatrician regarding the need for this test.
Limitations
- ⚠This test does not detect all types of genetic mutations, including large deletions/duplications or epigenetic changes.
- ⚠Variant of unknown significance may require further familial testing.
- ⚠Negative result does not completely exclude a metabolic disorder.
Risks & Considerations
- ●Discomfort during blood collection
- ●Bruising or bleeding from the venipuncture site
- ●Psychological impact of receiving genetic results
Interfering Factors
- ●Poor DNA quality or quantity
- ●Rare variants in introns or deep regulatory regions may not be detected
- ●Mosaic mutations may cause false negative results
- ●Consanguinity requiring parental confirmation
Compare With Similar Tests
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Frequently Asked Questions
What is the cost of CentoIEM NGS genetic test in India?
What is the CentoIEM NGS genetic test?
What is the sample type required for the CentoIEM test?
Do I need fasting before the test?
How long does it take to get the report?
Is home sample collection available?
What conditions does the CentoIEM test detect?
Is genetic counselling provided with the test?
Are there any risks involved in the test?
Can this test be done on children?
How is the CentoIEM test different from whole exome sequencing?
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Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
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