Overview
Leverage industry-leading long-read technology
Our laboratory is equipped with the PacBio® Vega™ system, providing up to 60Gbp per flow cell, HiFi data generation with 99.9% accuracy per read, and methylation calling without bisulfite treatment.
Deploy the tools to fit your data goals
Whether working with a single sample or scaling to hundreds, we work with a range of project sizes and specifications to return exactly the right data for your research—enough data to answer your questions without extraneous reads clogging downstream analysis.
Benefit from expert execution and review
With decades of combined experience in genomic sample processing across diverse research areas, our experts provide results you can trust to move your research forward with confidence.
Rest easy with secure data delivery
Data generated during your project is stored securely and available on our online portal—you control who has access and how long it remains available. Directly download FASTQ and BAM files with demultiplexed CCS HiFi reads and QC reports that include median read length, quality score, and duplication results.
Benefits
Find your perfect fit
Our service model is designed around your project, not the other way around. We work with you to generate precisely the data your study requires—no more, no less—at a budget aligned with your goals. Guided by a commitment to true partnership, we build collaborative, responsive relationships that keep your success at the center of everything we do.
Customize and optimize your sequencing pipeline
We operate as an extension of your laboratory, providing seamless integration into your research workflow. Our myReads NGS service packages offer a modular, flexible approach to project execution, designed to adapt efficiently and reliably to your project’s unique needs. Once your goals are set and the project has been appropriately scoped, we apply rigorous protocol adherence and thorough documentation practices to maintain consistency, reproducibility, and confidence in every result we deliver.
Working on a timeline? We work with you.
From clear project planning and transparent workflow overviews to reliable turnaround times—with options to expedite when needed—we keep your project moving forward. You’ll receive proactive, frequent communication on status and milestones (including sample arrival and condition, QC report, data delivery), along with high-touch support during critical moments.
High molecular weight extractions
Generating sufficiently pure, abundant high molecular weight (HMW) DNA is a critical initial step in any long-read project. We offer HMW DNA extraction services to set your project up for success from square one.
Contact us to inquire about high molecular weight DNA extractions.
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Applications
Daicel Arbor Biosciences has extensive experience in long-read sequencing pipelines, enabling a wide range of applications including:
- Detection of structural variants
- Improved genome assembly
- Improved resolution for repetitive regions
- Haplotype phasing
- Characterizing/mapping complex regions
- Epigenetics
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