Single Cell Sequencing
Revealing Biology One Cell at a Time
Every cell tells its own story. Traditional bulk sequencing blends signals across thousands or millions of cells, masking the cell-to-cell heterogeneity that drives development, disease, and therapeutic response. Single-cell sequencing unlocks this hidden complexity, providing a high-resolution view of genomes, transcriptomes, and epigenomes at the individual cell level.
At AUGenomics, we specialize in single-cell technologies that go beyond simple profiling. Our workflows integrate gene expression, immune receptor pairing, chromatin accessibility, and epigenetic modifications, giving researchers multi-dimensional insights into cellular states and functions.
Why Single-Cell Sequencing Matters
Single-cell sequencing has transformed life sciences by enabling researchers to:
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Resolve cellular heterogeneity in tissues, tumors, and immune responses.
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Map developmental trajectories and lineage relationships across time.
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Identify rare cell populations that play outsized roles in disease or therapy.
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Uncover regulatory networks linking chromatin state, gene expression, and cell identity.
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Accelerate drug discovery by revealing cell-type–specific responses to treatments.
From oncology to neurobiology, single-cell technologies are driving breakthroughs in precision medicine, basic biology, and therapeutic development.
Key Advantages of AUGenomics Single-Cell Services
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Multi-Omic Integration: Combine transcriptomics, receptor profiling, and epigenomics from the same cells.
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High-Resolution Clonal Tracking: Link immune receptor sequences with gene expression states.
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Flexible Platforms: Support for 10x Genomics, other droplet-based platforms, and nuclei-based workflows.
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Broad Sample Compatibility: Fresh or cryopreserved cells and nuclei from diverse tissues.
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Rare Cell Detection: Sensitive enough to capture low-frequency but biologically important populations.
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Customizable Workflows: Tailored solutions for specialized experimental designs.
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Advanced Bioinformatics: Includes clustering, trajectory analysis, receptor pairing, and integrated pathway analysis.
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Cross-Species Capability: Supports human, mouse, and other model and non-model organisms.
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Expert Support: Collaborative project design and data interpretation for complex studies.
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Rapid Turnaround: Standard delivery in 3–4 weeks, with accelerated options available.
What We Offer
Explore our full range of sequencing services: antifies alternative splicing events in single cells, contributing to the understanding of transcriptomic diversity.
Why Choose AUGenomics?
Scientific Precision – Reliable data with high depth and accuracy
Custom Flexibility – Tailored protocols to match your research goals
Fast Turnaround – Streamlined workflows with rapid results
Human Partnership – A responsive, collaborative team invested in your success
From early-stage discovery to clinical or translational research, we’re here to make your sequencing journey faster, easier, and more impactful.
Your Partner in Genomics
Not sure which method is best for your study? Whether you’re comparing whole exome sequencing vs. whole genome sequencing, exploring environmental DNA analysis, or need help with library preparation, we’re happy to guide you through the options.
We believe the best genomics work comes from real partnership—and we’re always ready to talk through your goals, questions, and challenges.
