Overview
ATAC Sequencing (Assay for Transposase-Accessible Chromatin sequencing) is a powerful technique used to assess genome-wide chromatin accessibility. It identifies regions of open chromatin, which are indicative of active regulatory elements such as promoters, enhancers, and insulators. By mapping these accessible regions, researchers can gain insights into gene regulation, epigenetic modifications, and disease mechanisms. DNA Labs India offers comprehensive ATAC-seq data analysis services, providing researchers and clinicians with accurate and actionable results. Our bioinformatics pipeline includes quality control, alignment to the reference genome, peak calling, annotation, differential accessibility analysis, and functional pathway enrichment. We also generate visualizations to facilitate interpretation. This service is ideal for studies in oncology, immunology, neurology, cardiovascular research, and metabolic disorders. With a cost of INR 18000, our service is competitively priced and includes a detailed report. We ensure high-quality analysis using state-of-the-art computational tools and experienced bioinformaticians. Whether you are exploring basic biology or translational research, our ATAC-seq analysis can help you uncover the regulatory landscape of the genome.
To be completed — reclassified from Tests on 2026-11-13.
The purpose of ATAC sequencing data analysis is to identify regions of open chromatin that are accessible to transcription factors and other regulatory proteins. This information helps in understanding gene regulatory networks, identifying potential biomarkers, and discovering therapeutic targets. It is widely used in cancer research to study tumor heterogeneity and epigenetic changes, in immunology to map immune cell differentiation, and in neurobiology to explore brain development and disorders. By providing a genome-wide view of chromatin accessibility, ATAC-seq analysis enables researchers to correlate epigenetic states with gene expression and phenotypic outcomes.
Sample requirements
What to send us
Deliverables & turnaround
What you receive
Turnaround: Reports are typically delivered within 4 weeks from the receipt of the sample and data.
Pricing
Transparent pricing
| Option | Turnaround | Price (INR) | Unit |
|---|---|---|---|
| Standard | Reports are typically delivered within 4... | ₹18,000 | per sample |
Limitations & precautions
What this service cannot do
Questions customers ask
Frequently asked questions
What is ATAC sequencing data analysis?
ATAC sequencing data analysis involves processing raw sequencing data from ATAC-seq experiments to identify open chromatin regions, perform peak calling, and interpret regulatory elements.
What is the cost of ATAC sequencing data analysis at DNA Labs India?
The cost is INR 18000, which includes comprehensive bioinformatics analysis and a detailed report.
What sample type is required for ATAC-seq analysis?
Extracted DNA of high quality is required. The DNA should be intact and free from contaminants.
How long does it take to get the results?
The turnaround time is 4 weeks from the receipt of the sample and data.
Is home sample collection available?
Yes, we offer free home sample collection for online bookings across major cities in India.
What does the analysis include?
The analysis includes alignment to reference genome, peak calling, annotation, differential accessibility, functional pathway analysis, and visualization.
Can ATAC-seq analysis be used for cancer research?
Yes, ATAC-seq is widely used in cancer research to identify regulatory elements involved in tumorigenesis and metastasis.
What is the difference between ATAC-seq and ChIP-seq?
ATAC-seq identifies open chromatin regions, while ChIP-seq identifies binding sites of specific proteins or histone modifications. ATAC-seq requires less input material and is faster.
Do I need to fast before providing a sample?
No, fasting is not required for ATAC-seq data analysis as it is a bioinformatics service.
Will I receive a report with interpretation?
Yes, the report includes detailed results, peak annotations, and pathway analysis, along with an interpretation guide.
Can I use my own sequencing data for analysis?
Yes, you can submit your raw sequencing data (FASTQ files) for analysis. Please contact us for data transfer instructions.
Is this test covered by insurance?
This service is typically not covered by insurance. However, you may check with your insurance provider for possible reimbursement.
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