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NGS Research Outsourcing Services

Outsource your NGS research to NTHRYS for whole genome sequencing, targeted sequencing, RNA-Seq, metagenomics, epigenomics, variant calling, and audit-ready NGS reports.

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NGS Research Outsourcing Services

Our Next Generation Sequencing (NGS) research outsourcing services provide high-throughput, accurate sequencing and bioinformatics support for diverse genomics projects in medicine, agriculture, and environmental sciences.

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Our NGS Research Capabilities

Our genomic scientists and bioinformaticians utilize cutting-edge sequencers, robust QC pipelines, and advanced data analytics to deliver comprehensive NGS results efficiently and securely.

Types of NGS Research We Handle

Key Research Outsourcing Services Offered

Why Choose Us for NGS Research Outsourcing?

Our team ensures high-quality sequencing, fast turnaround, robust data analysis, and full regulatory compliance for any NGS project across research and clinical domains.

Industries & Sectors We Serve

Customized NGS Solutions

We tailor sequencing depth, coverage, and analytical pipelines to match your specific project goals and regulatory needs for publication and submission.

Quality Assurance & Regulatory Compliance

Our workflows comply with GLP, GCP, ISO, and human genomic data protection standards, ensuring validated, reproducible, and audit-ready sequencing results.

Case Studies & Client Success Stories

See how our outsourcing has supported rare disease gene discovery, advanced oncology panels, and environmental microbiome surveillance. References available on request.

How It Works: Our Research Outsourcing Process

  1. Requirement Gathering: Define sample type, sequencing goals, and depth required.
  2. Proposal & Quotation: Provide a clear plan, platform selection, timeline, and cost estimate.
  3. Sequencing & Data Analysis: Perform library prep, sequencing run, and bioinformatics processing.
  4. Data Reporting: Deliver raw data, processed files, and compliance-ready reports.
  5. Post-Project Support: Offer re-analysis, publication help, and long-term data management.

Frequently Asked Questions (FAQs)

Q: What sequencing platforms do you use?
A: We use Illumina (short read) and ONT/PacBio (long read) for different project needs.

Q: Can you handle clinical-grade variant reporting?
A: Absolutely — we generate reports aligned with regulatory and clinical diagnostic guidelines.

Q: How is my sequencing data secured?
A: We follow strict NDAs, encrypted storage, and secure cloud sharing to protect your genomic data.

Get Started / Request a Quote

Contact us today to discuss your NGS project and receive a tailored plan, timeline, and cost estimate aligned with your research or clinical goals.

Contact Us

Email: research-outsourcing@nthrys.com
Phone: +91-8977624748

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