DNA & Genome Sequencing
Comprehensive Genomic Analysis for All Research Needs
DNA and genome sequencing form the foundation of modern genomics, enabling researchers to decode the complete genetic blueprint of any organism. From whole genome sequencing (WGS) to targeted panels, these technologies reveal genetic variation, structural changes, and evolutionary relationships with unmatched resolution.
At AUGenomics, we provide high-quality, flexible sequencing solutions tailored to your research goals. Our expertise spans human, model organisms, non-model species, microbial genomes, and more. Whether you need deep coverage for variant detection, long-read sequencing for structural analysis, or customized panels for focused targets, AUGenomics delivers data you can trust.
Why DNA & Genome Sequencing Matters
Genomic sequencing is central to breakthroughs in biomedicine, agriculture, ecology, and biotechnology. It allows researchers to:
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Identify genetic variants associated with disease, traits, or therapeutic response.
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Map genomes of non-model species for conservation or evolutionary studies.
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Uncover microbial diversity and functional capabilities in complex ecosystems.
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Support precision medicine through patient-specific genomic insights.
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Advance translational research by integrating genomics with transcriptomics and epigenomics.
With next-generation sequencing (NGS) and long-read technologies, AUGenomics provides a full spectrum of genomic analysis options to power discovery.
Key Advantages of AUGenomics DNA & Genome Sequencing
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Comprehensive Coverage: From small genomes to large, complex genomes across all species.
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Flexible Platforms: Short-read (Illumina) and long-read (PacBio, Oxford Nanopore) sequencing available.
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Customizable Workflows: Supports whole genome, exome, targeted panels, and custom assays.
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High Accuracy: Optimized protocols ensure high base-calling accuracy and uniform coverage.
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Low Input Compatibility: Effective sequencing from challenging or degraded samples.
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Advanced Bioinformatics: Variant calling, structural variant detection, genome assembly, and annotation included.
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Cross-Species Capability: Human, animal, microbial, plant, and environmental genomes supported.
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Multi-Omic Integration: Combine genomic data with transcriptomic or epigenetic layers for deeper insights.
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Expert Collaboration: Consulting support from project design through biological interpretation.
What We Offer
Our DNA and genome sequencing portfolio supports a wide range of research needs—from comprehensive genome-wide analysis to highly targeted applications. We offer flexible, customizable NGS services for human, animal, plant, and microbial projects.
Explore our full range of sequencing services:
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.
