Have questions? reach out
Have questions? reach out
WBL’s technology leverages the power of Nanopore long reads. Now equipped with clinically-viable sequencing accuracy and yield, long-read technologies are positioned to advance research and clinical diagnostics.
Long read PCR amplicon sequencing is particularly advantageous when investigating genomic regions that are challenging to sequence with short-read approaches. These include highly repetitive regions, structural variations, and other complexities.
Short Reads
ONT Long-Reads
DNA Sequence
Small Nucleotide Variants
Structural Variants
(Deletions, Insertions, Duplications, Inversions, Translocations)
Repetitive Regions
GC-Rich Regons
*WBL currently only accepts DNA and RNA that are extracted from samples that are not classified as infectious. This policy ensures the safety of our laboratory personnel and compliance with regulatory standards. Please ensure that all samples are appropriately treated and certified as non-infectious before submission. If you have any questions about sample preparation or our safety standards, please contact our support team at: support@wasatchbiolabs.com.
Accelerate your research with comprehensive nanopore data. With native precision and long reads, Wasatch BioLabs' Nanopore services deliver actionable insights with confidence in every read.
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Leverage Oxford Nanopore Technologies-certified services, supported by rigorous quality assurance and control metrics, to achieve reliable data for your research.
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Enhance your nanopore data with custom bioinformatics solutions, using tailored workflows and advanced analysis to generate impactful, publication-ready insights.
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Work directly with sequencing and bioinformatics experts who provide personalized, end-to-end support, guiding you from project planning to data interpretation.
PCR amplicon sequencing is a method that focuses on specific genomic regions by amplifying them using PCR and then sequencing the resulting amplicons. Wasatch BioLabs utilizes long-read nanopore sequencing to generate full-length reads of these regions, making it ideal for analyzing structural variants, SNPs, and complex or repetitive regions in targeted sequencing projects.
DNA samples extracted from humans, animals, plants, bacteria, and viruses are suitable for PCR amplicon sequencing, provided they are non-infectious. PCR amplicon sequencing is particularly well-suited for targets that are structurally complex, rich in GC content, or located within repetitive genomic regions where short-read sequencing struggles.
Yes, Wasatch BioLabs can design customized PCR amplicon sequencing workflows to meet unique research objectives. Whether targeting gene panels, rare mutations, or specific structural variants, our long-read sequencing approach ensures comprehensive and accurate coverage tailored to your study.
Our amplicon sequencing service includes robust bioinformatics support. Wasatch BioLabs delivers detailed data reports with variant calls, structural variant insights, and coverage metrics.
Our works closely with clients to ensure the sequencing results are not only accurate but also ready for interpretation and publication.
