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Bioinformatics service

Eukaryotic Transcriptome Sequencing Reference Based Data Analysis- Including lncRNA

Reviewed for accuracy
₹15,000
Per sample
final quote on confirmation
Results are typically available wi...
Turnaround
from sample receipt
Extracted DNA
Sample
input material
Enquiry
How to order
no payment online

Overview

Eukaryotic Transcriptome Sequencing Reference Based Data Analysis is a comprehensive genetic test that examines the complete set of RNA transcripts in a cell or tissue. This advanced technique uses next-generation sequencing (NGS) to quantify gene expression levels, identify alternative splicing events, and detect novel transcripts, including long non-coding RNAs (lncRNAs). lncRNAs are regulatory molecules that play critical roles in gene expression, chromatin remodeling, and cellular differentiation. Dysregulation of lncRNAs has been implicated in various diseases, including cancer, cardiovascular disorders, and neurological conditions. This test provides a reference-based analysis, meaning the sequenced reads are aligned to a reference genome to identify differentially expressed genes and pathways. The inclusion of lncRNA analysis adds a layer of regulatory insight, making this test valuable for research and clinical diagnostics. At DNA Labs India, we offer this test at an affordable cost of INR 15000, with home sample collection available across major cities. The test is performed using stringent quality controls and bioinformatics pipelines to ensure accurate and reproducible results. It is particularly useful for identifying biomarkers, understanding disease mechanisms, and guiding personalized treatment strategies.

To be completed — reclassified from Tests on 2026-11-13.

The purpose of this test is to analyze the transcriptome of eukaryotic cells to identify gene expression patterns associated with diseases. It helps in diagnosing genetic disorders, classifying cancers, predicting prognosis, and identifying potential therapeutic targets. The inclusion of lncRNA analysis provides insights into regulatory mechanisms that may not be evident from protein-coding genes alone.

Sample requirements

What to send us

Sample type: Extracted DNA
Volume: 1-2 µg
Container: Eppendorf tube
Collection: Blood or tissue biopsy

Deliverables & turnaround

What you receive

Turnaround: Results are typically available within 1 week after the sample reaches the lab.

Pricing

Transparent pricing

OptionTurnaroundPrice (INR)Unit
StandardResults are typically available within 1...₹15,000per sample

Limitations & precautions

What this service cannot do

Reference-based analysis may miss novel transcripts not in the reference
Low expression genes may not be detected
Requires high-quality RNA; degraded samples may yield poor results
Interpretation requires expert bioinformatics and clinical correlation

Questions customers ask

Frequently asked questions

What is the cost of the Eukaryotic Transcriptome Sequencing Reference Based Data Analysis including lncRNA?

The cost is INR 15000, which includes all steps from RNA extraction to bioinformatics analysis.

What is lncRNA and why is it important?

lncRNA stands for long non-coding RNA, which are RNA molecules longer than 200 nucleotides that do not code for proteins. They regulate gene expression and are implicated in various diseases.

What sample is required for this test?

The sample type is extracted DNA, but typically RNA is extracted from blood or tissue. Please confirm with the lab for specific requirements.

Is fasting required before the test?

No, fasting is not required for this test.

How long does it take to get the results?

Results are usually available within 1 week after the sample is received.

Can this test diagnose cancer?

This test can help in cancer diagnosis by identifying gene expression changes and biomarkers, but it is not a standalone diagnostic tool. Clinical correlation is essential.

Is home sample collection available?

Yes, we offer free home sample collection for online bookings across many cities in India.

What is the difference between transcriptome sequencing and whole exome sequencing?

Transcriptome sequencing analyzes all RNA transcripts, including non-coding, providing expression data. Whole exome sequencing focuses on protein-coding regions of DNA.

Are there any risks associated with the test?

The test involves a simple blood draw or biopsy, which carries minimal risks like bruising or infection.

How should I prepare for the test?

No special preparation is needed. Inform your doctor about any medications you are taking.

Can this test be used for research purposes?

Yes, it is widely used in research to study gene regulation, disease mechanisms, and biomarker discovery.

What is the turnaround time for reports?

The turnaround time is 1 week, and reports are delivered via online portal, email, or WhatsApp.


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Editorial accountability

Written by: Lookesh Sharma, Medical Content Writer
Reviewed by: Dr Pasupathy Arumugam , Consultant Pathologist
Last updated: 07 Sep 2026

DNA Labs India

Address: 2nd Floor, Prashanthi Arcade, 202, Amberpet Main Rd, Amberpet, Hyderabad - 500013, Telangana, India

Phone:+919395142800

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