Multiomics Services

Your Discovery Partner in All Things Genomics

We’re not just a service provider—we’re your research partner. With deep roots in genomics and over two decades of bioinformatics innovation, we help you crack the code on even the most complex multi-omics questions. From rare variant detection to integrated views of gene expression, protein dynamics, and epigenetic changes—We help your data speak in ways that drive discovery.
Total unique variants detected
0 M+
RNA samples sequenced
0 K+
Capabilities Research

Strand Research Advantage: Making Your Data Talk

Our Strength
Why It Matters
Automated Workflows
Seamless, high-throughput lab operations that scale with your needs
Comprehensive Reporting
Fast, reliable, and clinically validated results at your fingertips
Multi-Omics Expertise
Genomics, transcriptomics, proteomics, epigenomics—you name it, we integrate it
Curated Datasets
25+ years of refined, annotated data libraries to power your analysis
AI-Powered Analytics
From raw sequencing data to deep, research-grade insights—fast and accurate
Custom Study Design
End-to-end multiomics workflows built around your research goals—from sample to insight.

Multiomics Services

DNA Sequencing
  • Whole Genome Sequencing
  • Whole Exome Sequencing
  • Amplicon Sequencing
  • ChIP Sequencing
DNA Sequencing
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RNA Sequencing
  • Total RNA-Sequencing
  • mRNA Sequencing
  • Small RNA Sequencing
  • Spatial Transcriptomics
RNA Sequencing
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Microbial Sequencing
  • WGM (Shotgun metagenomics)
  • 16S rRNA
Microbial Sequencing
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Microarray Sequencing
  • Infinium Genotyping
  • Genome Wide Association Studies (GWAS)
  • Methylation Assays
  • Agrigenomics Consortium Arrays
Microarray Sequencing
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Epigenomics
  • Methylation sequencing
  • Targeted Methylation
  • Methylation Array
Epigenomics
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Integrated Multiomics
  • RNA-seq + DNA Methylation (WGBS / RRBS)
  • RNA-seq + ChIP-seq
  • RNA-seq + Whole Genome/Exome Sequencing
  • ATAC-seq + DNA Methylation
Integrated Multiomics
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Proprietary platform for unparalleled Variant Interpretation & Reporting

Strand NGS is a comprehensive platform designed for the analysis of NGS data

Who do we serve

Academic Research
We empower university researchers, grant-funded projects, research institutions, and PhD students with advanced bioinformatics tools and solutions for genomics studies.
Industrial Research
Industrial Research

We are partner with biotech companies and life science industries to optimize research and development with custom data analysis pipelines that accelerate innovation.

Seed Industry
Seed Industry

We enable breeding programs, support crop improvement research, and provide tools for trait and marker development, advancing Agri genomics research.

Pharma Industry
Pharma Industry

We drive precision medicine, support clinical trial analysis, and facilitate biomarker and drug development to improve therapies by understanding disease mechanisms.

Our Associated Partners

Insights

Latest articles, case studies, publications & posters based on trending info on the right.
Exome-Plus in the Detection of Early Onset Bone Marrow Failure
Characterization of Signaling Pathways in Solid Tumors Using Comprehensive Genomic Profiling
Evidence-Driven Reclassification of VUS: Impact on Genetic Counseling and Surveillance
Patient Awareness Resources
An analysis of likely germline events by tumor tissue testing on large somatic panels.
A minimal comprehensive somatic panel to aid clinical decision making in a low cost setting.
How Millets Talk to Fungi: A Transcriptomic Perspective
Evaluating Methylation Signatures: Principles, Techniques, Targeted Methylome Panels, and Methylation Arrays
Unlocking CAR T-Cell Innovation: How CITE-seq is Revolutionizing Immunotherapy Research
Key Insights from 1200+ Strand HRD Reports
Strand Life Sciences: Unlocking Millet-Fungi Symbiosis
Rare Neurometabolic Disorder: Investigating Leigh Syndrome with SURF1 Gene Mutations
The Importance of HRD Testing Over BRCA1/2 for PARP Inhibitor Therapy (Intl)
Navigating BRCA1 VUS in High-Grade Serous Peritoneal and Endometrial Carcinomas
Revealing Hidden Microbial Diversity Through NGS Technology
Building methylation workflows for the clinic: A Strand Life Science Perspective
Comprehensive RNA-seq Analysis in Strand NGS
Harnessing RNA Seq for Functional Insights
Lynch syndrome: An unusual case of familial cancer unearthed
Charcot-Marie-Tooth disease type 2S: identical novel missense mutation of IGHMBP2 gene in two unrelated families

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