Introducing Our Custom Sequencing Service: Discovery Mode

You aren't doing "standard" science, so why should you settle for standard sequencing?

We know that every breakthrough begins with a unique question. Whether you're hunting for a rare variant, mapping a non-model organism, or pushing the boundaries of synthetic biology, the data you collect has to be tailored to your project.

That’s why we are beyond excited to officially announce the launch of our custom sequencing service, called Discovery Mode.

Why Long Reads?

The biological truth is often hidden in the parts short-reads can’t reach. By capturing fragments that are tens (or even hundreds) of kilobases long, our service allows you to:

• Resolve Structural Variants: Finally see the inversions, translocations, and large insertions that short-reads routinely miss.
• Phase Haplotypes: Distinguish between alleles with confidence and map maternal vs. paternal contributions accurately.
• Close Genome Gaps: Turn your fragmented assemblies into high-quality, complete genomes by spanning repetitive regions with long reads.
• Build High-Quality Reference Sequences: Generate "gold standard" de novo assemblies for non-model organisms.
• Screen PCR Pools & Complex Amplicons: Sequence through long-range PCR products and complex pools in a single pass to verify orientation and integrity.

Transparent, Modular Pricing

We believe you should only pay for what you actually use. No hidden "processing fees" or bundled packages that include data you don't need. Our pricing is straightforward and scales with your project, whether you need 1 billion bases (1 Gb) or hundreds. Prices are in Canadian Dollars and subject to local tax.

What You Get: Data & Deliverables

We aren't just a data factory; we’re your collaborators. When your run is complete, we don't just send a "good luck" email. Our standard delivery package includes:

1. Raw Data (FASTQ): High-fidelity, base-called reads ready for your pipeline, using the best available basecallers.
2. Comprehensive QC Report: Detailed metrics on read length N50, total yield, and base quality scores so you know exactly what you’re working with.
3. Human review: A real human takes a look at the results to make sure they meet our internal standards.

Need a head start on the science? If your lab's bioinformatic pipeline is already at capacity, we offer Additional Analysis as an add-on service. From alignment (BAM files) and variant calling (VCFs) to full de novo assembly, our team can handle the heavy lifting for you. Contact us for more information.

Ready to build your run?

Log in to easily a quote. Let’s get you the data your project demands, quickly.