Single-Cell RNA Sequencing (scRNA-seq) Service
Move beyond the average to decode cellular complexity. While bulk sequencing provides a blended view of a tissue, our Single-Cell RNA Sequencing (scRNA-seq) service delivers the exact functional state of every individual cell. By mapping true cellular heterogeneity, we enable researchers and industrial partners to pinpoint rare cell populations, track lineage trajectories, and identify specific cellular drivers of disease. Enhance your pre-clinical pipeline by uncovering the high-resolution molecular mechanisms that bulk data simply obscures.
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- Platforms
- Workflow
- Deliverables
- Applications
- Why choose
- FAQs
- Sample preparation
Our Technology & Platforms
We utilize industry-leading platforms to ensure high capture efficiency and data sensitivity. Whether you are looking for high-throughput screening or deep sequencing of specific populations, we have the right pipeline:
- 10x Genomics Chromium: The gold standard for high-throughput 3' or 5' gene expression, V(D)J profiling, and Multiome (ATAC + GEX).
- BD Rhapsody: High-efficiency microwell-based capture, excellent for targeted panels and CITE-seq (proteogenomics).
Comprehensive Workflow

Project Deliverables
We provide a comprehensive data package designed for immediate interpretation and publication-ready results. Our goal is to ensure you spend less time processing raw files and more time focused on your biological discoveries.
- Raw & Processed Data Files
- Raw Sequence Data: Standard .fastq.gz files containing your raw reads.
- Alignment & Quantification: Feature-barcode matrices (filtered and unfiltered) in .h5 or .mtx formats.
- Read Mapping Reports: Summary files detailing sequencing saturation, mapping rates, and cell recovery metrics.
- Advanced Bioinformatics Package
- Dimensionality Reduction: High-resolution UMAP and t-SNE coordinates for visualizing cell clusters.
- Differential Expression (DE): Comprehensive lists of marker genes for every identified cell cluster.
- Quality Control Logs: Detailed documentation of cell filtering, doublet detection, and normalization steps.
- Interactive Visualization & Reporting
- Software-Compatible Files: Ready-to-load files for platforms like 10x Genomics Loupe Browser, Seurat, or Scanpy.
- Publication-Quality Figures: High-resolution plots of cluster assignments, heatmaps, and violin plots of your genes of interest.
Applications
- Identify Rare Subpopulations: Detect elusive cell types, such as circulating tumor cells or specific stem cell niches, that are often masked in bulk data.
- Map Dynamic Cell States: Track how individual cells evolve, differentiate, or respond to therapeutic interventions over time.
- Characterize Complex Tissues: Define the diverse cellular composition of healthy and diseased tissues with unparalleled clarity.
- Discover Novel Biomarkers: Locate specific gene expression signatures unique to distinct cell clusters to fuel your next stage of drug discovery or clinical research.
Why Choose Our Service?
- Expert Sample Dissociation: Specialized protocols for fragile or complex tissues (e.g., tumor, brain, lung) to ensure high viability and minimal cell stress.
- Scalable Multi-Omics: Integrated support for CITE-seq (proteomics), V(D)J profiling, and cell hashing to maximize data from every cell.
- Rigorous Quality Control: Multi-stage checkpoints—from suspension to library prep—to guarantee sequencing efficiency and minimize batch effects.
- Actionable Bioinformatics: We deliver publication-ready clusters, differential expression analysis, and interactive visualization tools.
FAQs
How many cells should I target per sample?
For most discovery-based projects, we recommend targeting 5,000 to 10,000 cells per sample. This typically provides sufficient statistical power to identify subpopulations representing at least 1–5% of the total sample.
How do you handle batch effects?
We utilize Cell Hashing (oligo-tagged antibodies) to multiplex samples into a single lane. This significantly reduces technical variability and lowers the per-sample cost of library preparation.
What species are compatible with your service?
Our primary pipelines support Human and Mouse (using established reference genomes). However, we can process any species with a well-annotated reference genome. Please consult with our team for non-model organisms.
Learn about other Q&A.
Sample Submission Guideline
| Category | Requirement | Technical Specification |
|---|---|---|
| Cell Viability | Minimum Threshold | >80% viability (measured via Trypan Blue or AO/PI). |
| Total Cell Count | Minimum Submission | At least 50,000–100,000 cells in suspension to account for loading loss. |
| Suspension Buffer | Recommended Media | PBS (Ca²⁺/Mg²⁺-free) supplemented with 0.04% BSA. |
| Purity | Debris & Clumping | Must be a single-cell suspension; filtered through a 30µm–40µm mesh to remove aggregates. |
| Contaminants | Red Blood Cells (RBCs) | RBC lysis is required for blood or highly vascularized tissue samples. |
| Buffer Exclusions | Prohibited Reagents | No EDTA (>0.1mM), surfactants (SDS/Tween), or high glycerol concentrations. |
| Sample Volume | Minimum Volume | Provide at least 50µL – 100µL of cell suspension per sample. |
NOTE: For detailed submission instructions, please contact our technical team.


