The sequencing marketplace with expert NGS guidance for every researcher. We advise on the best strategy, match you with the right provider, and manage it end to end, from sample collection to result delivery.
What We Offer
From high-throughput Next-Generation sequencing to classical Sanger and deep bioinformatics, everything under one roof.
High-throughput NGS for any application, Whole Genome, RNA-seq, Amplicon sequencing and more. High capacity with fast Turnaround Time.
Classic Sanger sequencing with high accuracy for clone verification, point mutations, and genotyping. Results within 24–48 hours.
Comprehensive bioinformatics: from mapping and assembly to functional analysis, visualization, and detailed reports.
How It Works
You bring the experiment idea. From consultation, through the quote, to final results, we handle everything else.
You bring the experiment idea, and our NGS experts advise on the best strategy and study design.
We match you with the right provider and send a clear, formal quote within one business day.
We arrange sample collection and manage library prep, sequencing, and quality checks, all for you.
Raw data and/or a full bioinformatics report, delivered via secure portal.
Why QuickSeq
Backed by 20+ years of hands-on experience in sequencing and genomics, from experimental design to publication-ready data.

Rush, standard, or scheduled, choose the TAT that fits your timeline and budget.

Rigorous QC at every step to support publication-quality data.

Two decades of hands-on experience in NGS, Sanger, and bioinformatics, guiding researchers from design to discovery.

Encrypted transfer and secure storage. Full NDA available upon request.

A dedicated NGS scientist guides your project, from experimental design to the final report.

Transparent per-sample prices up front, with volume discounts on larger projects and a formal quote within one business day.
Get Started
Three ways to reach us, choose what works best for you.