Genomics
Comprehensive genome analysis for human, animal, plant, and microbial research.
- Whole Genome Sequencing
- Genome Resequencing
- De novo Assembly
- Structural Variant Analysis
- Population Genomics
Precision sequencing for global research
Precision Genomics.
Scalable Insights.
End-to-end sequencing and multi-omics solutions for life science, biotech, agricultural, microbial, and translational research teams worldwide.
6+
Core service modules
Global
Research support
Fast
Turnaround workflow
Service Focus
Whole Genome Sequencing
Service Focus
RNA-seq & Full-length Transcriptomics
Service Focus
DNA Methylation & ATAC-seq
Service Focus
Single-Cell & Spatial Omics
Service Focus
Shotgun Metagenomics
Service Focus
Bioinformatics & Multi-omics Integration
Services
A complete sequencing and omics portfolio
Our service framework is designed for academic laboratories, biotech companies, CRO collaborations, and translational research programs that require dependable data and interpretable results.
Transcriptomics
High-resolution gene expression and RNA structure analysis for discovery and validation studies.
- Bulk RNA-seq
- Full-length Transcriptome Sequencing
- Alternative Splicing Analysis
- lncRNA / circRNA Analysis
- Small RNA Sequencing
Epigenomics
Interrogate regulatory biology beyond sequence alone.
- DNA Methylation Sequencing
- ATAC-seq
- ChIP-seq
- Hi-C / 3D Genome
- DNA-Protein Interaction Analysis
Single-Cell & Spatial Omics
Resolve heterogeneity at cellular and tissue levels.
- Single-cell RNA Sequencing
- Single-cell ATAC Sequencing
- Immune Repertoire Profiling
- Spatial Transcriptomics
- Tissue Architecture Analysis
Microbiome & Metagenomics
Microbial profiling for clinical, environmental, and industrial studies.
- 16S/18S/ITS Amplicon Sequencing
- Shotgun Metagenomics
- Pathogen Detection
- Microbial Diversity Analysis
- Resistance Gene Profiling
Bioinformatics & Multi-omics
From raw reads to publication-ready interpretation.
- Genome Assembly & Annotation
- Variant Calling
- Transcript Quantification
- Functional Enrichment Analysis
- Multi-omics Data Integration
Technology
Platform flexibility for complex research designs
Different biological questions require different read architectures. We support both short-read and long-read strategies, paired with rigorous QC and downstream analytics.
Short-read sequencing
High-throughput, highly accurate workflows for RNA-seq, resequencing, mutation detection, and large-scale cohort studies.
- Cost-efficient for production-scale studies
- Ideal for quantification-heavy designs
- Well-suited for variant calling and expression profiling
Long-read sequencing
Enhanced structural resolution for complex genomes, repeat regions, transcript isoforms, and metagenomic assemblies.
- Improved de novo assembly continuity
- Isoform-level transcript analysis
- Better detection of large structural rearrangements
Applications
Built around real scientific questions
Good sequencing is not merely data generation. It is experimental fit, sample logic, turnaround discipline, and analysis that answers the original biological question instead of producing an expensive pile of files.
Human Health
Rare disease research, cancer genomics, biomarker discovery, precision medicine, and translational workflows.
Agriculture & Breeding
Crop genomics, trait mapping, breeding support, and comparative analysis for plant and animal improvement programs.
Microbiome
Human microbiome, environmental community profiling, industrial microbiology, and pathogen surveillance.
Drug Discovery
Mechanism-of-action studies, target validation, pharmacogenomics, and response stratification.
Microbial Genomics
Bacterial, fungal, and viral genomic projects including comparative genomics and outbreak-related investigations.
Custom Research
Tailored project design for studies that are too specific to fit inside a neat brochure box. Science has never respected neat brochure boxes anyway.
Workflow
From project brief to interpretable delivery
1
Project Consultation
2
Study Design Review
3
Sample Preparation
4
Sequencing Execution
5
Bioinformatics Analysis
6
Report & Data Delivery
Pricing
Example project packages
Final pricing depends on sample type, throughput, read configuration, and analysis scope. These starter ranges make the website feel commercial instead of decorative, which is generally a good habit for a company that intends to invoice people.
Popular
RNA-seq Package
From $490
per project entry level
- Library preparation guidance
- Sequencing execution
- QC report
- Basic differential expression analysis
Research
Genome Package
From $1,290
depending on design
- Whole genome sequencing
- Variant calling pipeline
- Alignment files and report
- Optional annotation support
Advanced
Single-Cell Package
Custom Quote
project-specific scope
- Experimental planning
- Single-cell workflow support
- Cell clustering and marker analysis
- Downstream interpretation
FAQ
Questions serious buyers usually ask
What data formats are delivered?
Typical deliverables include FASTQ, BAM, VCF, count matrices, QC summaries, and analysis reports depending on workflow scope.
Can you support custom analysis requests?
Yes. Bioinformatics scope can be adapted to publication-oriented, exploratory, or translational study designs.
Do you work with international clients?
Yes. The website is structured for global research support, including remote consultation and digital data delivery.
How quickly can a quote be returned?
Most inquiry reviews can be answered within one business day if the sample type and project objective are clear.
Contact
Start your next sequencing project
Tell us the organism, sample type, target application, sample count, and expected analysis scope. The more specific the brief, the less time everyone spends performing interpretive archaeology on vague emails.