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.
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
- Whole Genome Sequencing (WGS)
- Whole Exome Sequencing (WES)
- Targeted Gene Panel Sequencing
- RNA Sequencing (RNA-Seq)
- Small RNA Sequencing
- Transcriptome Assembly
- De Novo Genome Assembly
- Resequencing and Variant Discovery
- SNP and Indel Calling
- Structural Variant Analysis
- Copy Number Variation (CNV) Analysis
- DNA Methylation Sequencing
- ChIP-Seq for Protein-DNA Interaction
- ATAC-Seq for Chromatin Accessibility
- Hi-C for 3D Genome Mapping
- Single Cell RNA-Seq
- Metagenomic Sequencing
- Microbiome Profiling
- Pathogen Genome Sequencing
- Viral Genome Surveillance
- Plant and Animal Genome Projects
- Epigenomics and Regulatory Regions
- Gene Fusion Detection
- Oncology Targeted Panels
- Rare Disease Variant Analysis
- Population Genomics Studies
- Publication-Ready NGS Data
- Regulatory-Compliant NGS Reports
- Cross-Lab Collaborative NGS Projects
- Custom NGS Research Projects
Key Research Outsourcing Services Offered
- Sample Preparation and QC
- Library Construction and Indexing
- Sequencing on Illumina/ONT Platforms
- Base Calling and Quality Filtering
- Read Alignment and Mapping
- Variant Calling and Annotation
- Transcriptome Assembly and Quantification
- ChIP-Seq and ATAC-Seq Analysis
- Epigenetic Data Interpretation
- Single Cell Sequencing Pipelines
- Microbiome Taxonomic Profiling
- Metagenomic Pathogen Detection
- Custom Bioinformatics Workflows
- Data Visualization and Reporting
- Publication-Ready Figures and Tables
- Regulatory-Compliant Documentation
- Confidential Data Handling and NDA
- Interim Reports and Project Updates
- Data Sharing on Secure Cloud Platforms
- Stakeholder Presentation Support
- Workshops and Training in NGS Analysis
- Post-Project Technical Consulting
- IP and Patent Filing Support
- Grant Proposal and Manuscript Assistance
- Sample Archiving and Secure Backup
- Compliance with GLP, GCP, ISO Standards
- Cross-Lab Data Validation and Sharing
- Collaboration with Clinical and Academic Labs
- Long-Term NGS Research Partnerships
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
- Medical Genomics and Diagnostics
- Pharmaceutical R&D Divisions
- Agrigenomics and Plant Breeding Companies
- Microbiome and Metagenomics Labs
- Environmental Genomics Agencies
- Academic and Clinical Research Centers
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
- Requirement Gathering: Define sample type, sequencing goals, and depth required.
- Proposal & Quotation: Provide a clear plan, platform selection, timeline, and cost estimate.
- Sequencing & Data Analysis: Perform library prep, sequencing run, and bioinformatics processing.
- Data Reporting: Deliver raw data, processed files, and compliance-ready reports.
- 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
Contact Us