Daicel Arbor Biosciences launches myReads® Long-Read Whole Genome Sequencing

Ann Arbor, MI, March 31, 2026 – Daicel Arbor Biosciences is introducing a new myReads^® long-read whole genome sequencing (WGS) service, delivering high-accuracy sequencing with the flexibility, expertise, and support researchers need to move their projects forward. Powered by PacBio HiFi long-read technology, myReads long-read WGS enables deeper insight into complex genomes, resolving structural variation, repetitive regions, and other challenges that often fall beyond the reach of short-read sequencing. Whether it’s a single sample or a larger study, the goal is simple: deliver the right data for the question at hand.

“Our new myReads long-read whole genome sequencing service is designed to make long-read sequencing more accessible and practical for researchers,” said Jennifer Klunk, Ph.D., Senior Product Manager – Genomics Services, at Daicel Arbor Biosciences. “By combining advanced technology with our expert support and flexible workflows, we’re helping researchers generate high-quality data that will help them move forward with more confidence than ever before.”

myReads long-read WGS offers a modular, end-to-end service model. This includes high molecular weight (HMW) DNA extraction, SMRTbell library preparation, sequencing on the PacBio Vega system, and optional bioinformatics analysis. Researchers also benefit from accurate HiFi reads (99.9%), methylation detection without bisulfite treatment, and support for challenging sample types.

Data is then delivered through a secure online portal, with access to FASTQ and BAM files, demultiplexed CCS HiFi reads, and detailed QC reports.

From genome assembly and structural variant detection to epigenetics and haplotype phasing, myReads long-read WGS empowers researchers to tackle complex genomic questions—without the complexity.

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