Introducing RhinoSeq™
The Fastest, Simplest Library Prep Kit for Your Illumina Sequencer
Library Prep in 20 Minutes
The Power to Change NGS
KEY BENEFITS
RhinoSeq enzymatically cleaves dsDNA samples for whole genome sequencing with minimal GC bias and high-quality reads.
Fast
3 Step Protocol
Simple
Single Tube
Accurate
Reduces Errors
Automation
Flexible Format
Easy
Less Hands-On
LATEST NEWS AND BLOG POSTS
Understanding NGS Library Complexity: Sources of Sequencing Errors & Limits of Detection
Next-generation sequencing is, by definition, “massively parallel.” While the first 454/Curagen GS20 systems yielded a million reads per run, the latest sequencing platforms from Illumina, (NovaSeq 6000 running their highest-capacity S4 flowcell), yields 10,000X the [...]
Introducing the SeqOnce and Done Blog and the Team Behind the Technology
SeqOnce is a company founded upon the idea that steps involved in Next Generation Sequencing (NGS) need to be both streamlined and simplified. Having developed and launched the first product, RhinoSeq, NGS library preparation time [...]
RhinoSeq ABRF Poster 2019 – A 12-Min, Single Tube, Nanogram Input, Library Prep
Current next Generation Sequencing (NGS) library construction is a bottleneck in the sequencing workflow. The processes of library construction for DNA and RNA sequencing are complex, error prone, costly, and time consuming. Current commercial products [...]