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DNA Labs India

Aptamer Sequencing and Analysis Test

DNA Labs India | ISO 9001:2015 Certified

Aptamer Sequencing and Analysis Test

Short Name: Aptamer Seq

Also known as: Aptamer NGS, Aptamer Sequencing

Aptamer Sequencing and Analysis Test test available at DNA Labs India for ₹30,000. Uses Next-Generation Sequencing (NGS), Bioinformatics Analysis on Extracted DNA samples. Results in Reports are delivered within 8 weeks from sample receipt.. Free home collection in 300+ cities across India.

Sequencing🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of aptamer sequencing and analysis is to determine the nucleotide sequences of aptamers within a library, identify those with high binding affinity to a specific target, and provide quantitative data on their enrichment. This information is crucial for selecting lead aptamer candidates for further development in diagnostics, therapeutics, and biosensing applications.

Test Code
6358
CPT Code
0000A
ICD Code
Z00.00
Price
₹30,000
Sample Type
Extracted DNA
Result Time
Reports are delivered within 8 weeks from sample receipt.
Fasting Required
No
Method
Next-Generation Sequencing (NGS), Bioinformatics Analysis
Step 1

Sample Collection

No special preparation is required. Ensure the extracted DNA sample is of high quality and free from contaminants.

Method: Blood or extracted DNA

Step 2

Laboratory Analysis

Sample collection is performed by trained phlebotomists. For extracted DNA, provide the sample in a sterile, labeled tube.

Step 3

Report Delivery

The sample should be transported to the laboratory at the earliest, preferably on ice or at 4°C. No specific aftercare is needed.

Timeline: Reports are delivered within 8 weeks from sample receipt.

Patient Instructions

1
Before the Test:No special preparation is required. Ensure you have a valid prescription or research protocol.
2
During the Test:The sample is processed in the laboratory. No action is needed from the patient.
3
After the Test:You will receive the report via email/portal. Discuss results with your healthcare provider or research team.

About This Test

Who Should Get This Test

The purpose of aptamer sequencing and analysis is to determine the nucleotide sequences of aptamers within a library, identify those with high binding affinity to a specific target, and provide quantitative data on their enrichment. This information is crucial for selecting lead aptamer candidates for further development in diagnostics, therapeutics, and biosensing applications.

How to Prepare

  • For blood collection, use EDTA or citrate tubes.
  • For extracted DNA, ensure concentration is at least 50 ng/µL.
  • Label the sample with patient ID and date.
  • Maintain cold chain during transport.

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"Aptamer sequencing is a powerful tool for identifying high-affinity binders. Our analysis pipeline ensures accurate sequence identification and quality control, supporting research and diagnostic applications."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeExtracted DNA
Sample Volume1-2 µg
ContainerEppendorf tube
Collection MethodBlood or extracted DNA

Sample Stability

Extracted DNA: stable at -20°C for 6 months
Blood: stable at 4°C for 24 hours
Avoid repeated freeze-thaw cycles
Sample Rejection Criteria:
  • Hemolyzed blood samples
  • Insufficient DNA quantity (<1 µg)
  • Degraded DNA (low molecular weight)
  • Improper labeling

Understanding Your Results

The results of aptamer sequencing and analysis provide a comprehensive profile of the aptamer library. Enriched sequences with high read counts and significant fold changes are considered potential candidates for further validation. The report includes sequence data, quality metrics, and enrichment analysis to guide your selection process.
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Sequences with fold change >2 are considered significantly enriched and may represent high-affinity aptamers.

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A high diversity indicates a complex library, while low diversity may suggest over-amplification or loss of variants.

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Optimal GC content (40-60%) ensures stable secondary structures and efficient amplification.

⚠️ When to Consult a Doctor:

If you are developing aptamer-based diagnostics or therapeutics, consult with a molecular biologist or geneticist to interpret the sequencing results and plan next steps. For clinical applications, discuss with a qualified medical professional.

Limitations

  • Requires high-quality extracted DNA
  • Bioinformatics analysis may not predict binding affinity accurately
  • Results depend on library complexity and SELEX enrichment
  • Not a diagnostic test for any specific disease

Risks & Considerations

  • No significant risks associated with blood draw
  • Possible bruising at venipuncture site
  • Rare infection if proper hygiene is not maintained

Interfering Factors

  • Contamination with genomic DNA
  • Degraded RNA/DNA samples
  • PCR amplification bias
  • Incomplete adapter ligation
  • Low sample concentration

Compare With Similar Tests

TestAptamer Sequencing and Analysis
ComparisonAptamer Sequencing and Analysis

Frequently Asked Questions

What is aptamer sequencing?
Aptamer sequencing is a process that determines the nucleotide sequence of aptamers in a library, typically using high-throughput NGS, to identify high-affinity binders.
What is the cost of aptamer sequencing at DNA Labs India?
The cost is INR 30,000 per sample, which includes sequencing, bioinformatics analysis, and a detailed report.
What sample type is required?
Extracted DNA is required. The sample should be of high quality with a concentration of at least 50 ng/µL.
How long does it take to get results?
The turnaround time is approximately 8 weeks from sample receipt.
Is fasting required before sample collection?
No, fasting is not required for this test.
Can I get a home sample collection?
Yes, we offer free home sample collection for online bookings across major cities in India.
What is the difference between NGS and Sanger sequencing for aptamers?
NGS provides high-throughput sequencing of millions of aptamer molecules simultaneously, while Sanger sequencing is limited to single sequences. NGS is preferred for aptamer libraries.
What kind of analysis is included?
Our analysis includes quality control, adapter trimming, sequence alignment, enrichment analysis, and diversity metrics.
Can this test be used for clinical diagnosis?
This test is primarily for research and development. It is not intended for direct clinical diagnosis of any disease.
What are the applications of aptamer sequencing?
Applications include developing diagnostic assays, therapeutic aptamers, biosensors, and biomarker discovery.
How should I store my extracted DNA sample?
Store at -20°C or below. Avoid repeated freeze-thaw cycles.
Do you provide a report with the results?
Yes, a comprehensive report with sequence data, enrichment analysis, and quality metrics is provided.
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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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.

LIMS Integration

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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