Uncover what remains hidden with short-read sequencing: large structural variants and complex, repetitive regions of the genome. High-accuracy long reads lift whole genome sequencing (WGS), panel sequencing, whole genome methylation sequencing (WGM), and full-length 16S sequencing to the next level.
Our established long-read products, powered by PacBio’s Revio system, deliver high-accuracy data, rapid turnaround, and unmatched cost-efficiency. Sequence up to 40 human genomes per week for under 1,000 € per sample (pricing depends on project size) — ideal for large-scale studies or population genetics.
Need deeper insights? Add methylation profiling or leverage our advanced bioinformatics pipeline to extract maximum value from your sequencing data.
Explore Our Long-Read Sequencing Product Portfolio
Long-Read Sequencing on PacBio’s Revio
With the PacBio Revio system in place, we deliver long-read sequencing at scale. The Revio system combines accuracy, speed, and throughput in one powerful solution.
Revio’s single-molecule real-time (SMRT) technology delivers HiFi reads by sequencing individual DNA molecules multiple times. The result: long reads with exceptional per-base accuracy — ideal for detecting structural variants, resolving repeats, and unlocking for short-read inaccessible regions of the genome.
The Revio system efficiently enables sequencing of up to 40 whole human genomes per week. With low DNA input requirements and integrated data processing, Revio accelerates timelines without compromising quality.
Our products based on the Revio systems give you exactly what your research demands: depth, accuracy, and results you can act on.
Fuel your research with long-read sequencing at its best. Our Revio-powered products deliver exceptional results across HiFi Whole Genome Sequencing, HiFi Whole Genome Methylation, targeted HiFi panels, and Full-Length 16S Sequencing. High accuracy, high throughput — built for your most demanding projects.
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Do you have a question or are you interested in our service? Feel free to contact us. We will take care of your request as soon as possible.
Start Your Project with Us
We are happy to discuss sequencing options and to find a solution specifically tailored to your clinical study or research project.
When getting in contact, please specify sample information including starting material, number of samples, preferred library preparation option, preferred sequencing depth and required bioinformatic analysis level, if possible.
