Next Generation Sequencing Next Generation Sequencing Systems Products & Reviews

Easy Transition from Manual NGS Library Prep. Compact and efficient, the NGS STARlet is an automated solution for NGS library preparation, combining intuitive software with optimized methods to reduce hands-on time and variability.

The MiSeqDx instrument is the first and only FDA-cleared in vitro diagnostic (IVD) next-generation sequencing (NGS) system. Designed specifically for the clinical laboratory environment, the MiSeqDx instrument offers a small, approximately 4 square feet (0.37 square meters) footprint, an easy-to-follow workflow, and data output tailored to the needs of clinical labs. In addition, the integrated software enables sample trackin…

The next level in diagnostic power for the clinical lab

Scalable throughput and flexibility for virtually any sequencing method, genome, and scale of project.

Fast workflow and robust performance from a few to hundreds of genes, with as little as 1 ng input

The Twist Human Comprehensive Exome Panel offers over 99% coverage of protein-coding genes, providing a solution for exome sequencing with high performance and flexibility.

Fast and affordable next-generation benchtop sequencer

Introducing the next-generation sequencing system for the molecular diagnostic laboratory.   The Ion PGM™ Dx Instrument System* will deliver the speed and simplicity of the Ion Torrent™ platform, combined with key workflow advantages designed specifically for regulated laboratory environments and in vitro diagnostic applications. Used in conjunction with Ion PGM™ Dx library kits, Ion One Touch™ Dx template kits,…

The new Sequel System is based on Pacific Bioscience’s proven Single Molecule, Real-Time (SMRT) technology and delivers about 7X more reads with 1 million zero-mode waveguides (ZMWs) per SMRT Cell. The Sequel System is ideal for projects such as rapidly and cost-effectively generating high-quality whole genome de novo assemblies. This innovative sequencing system features automated reagent and SMRT Cell handling and an inte…

Simple, reproducible automated sequencing  

The Chromium x Series lets you access single cell analysis at any stage. From Chromium ix, offering cost-effective, lower throughput single cell analysis, upgradable to the high-throughput full-range Chromium x, single cell analysis is made a perfect fit.

The PacBio RS II is a Single Molecule, Real-Time (SMRT®) DNA Sequencing System that provides the highest consensus accuracy and longest read lengths of any available sequencing technology. SMRT Sequencing is ideal for de novo assembly, characterization of genetic variation, methylation analysis, microbiology studies, and more.The instrument features high performance optics, automated liquid handling, and an environmental cont…

The Ion S5™ next-generation sequencing system enables a simple targeted sequencing workflow for your lab at an affordable price, without compromising on performance or reliability. The Ion S5 System leverages the speed of semiconductor sequencing with impressive on-board computing power, to enable the production of high quality sequencing data in as little as 2.5 hours and enable you to go from DNA library to data in a…

The power of next-gen sequencing in your hands. The GS Junior System brings the power of 454 Sequencing Systems directly to the laboratory benchtop. Get comprehensive genome coverage with long 400 bp sequencing reads and quickly proceed from DNA to discovery with fast sequencing runs and straightforward data analysis on the attendant computer.GS Junior System Features: Powered by proven technology: Uses GS Junior Titanium…

Now delivering sequencing reads up to 1,000 bp in length! The GS FLX+ System features the unique combination of long reads, exceptional accuracy and high-throughput, making the system well suited for larger genomic projects. The GS FLX System has been at the heart of key breakthrough genomic discoveries and over 1,000 peer-reviewed publications to date.Advancements in sequencing chemistry, instrumentation and software offer t…

The Roche Genome Sequencer FLX System, powered by 454 Sequencing, enables ground-breaking discoveries in de novo sequencing, resequencing of whole genomes and target DNA regions, metagenomics, and RNA analysis. Featuring a unique combination of long reads, exceptional accuracy, and ultra-high throughput, the Genome Sequencer FLX System delivers the most comprehensive result at a low total cost, giving it the best overall value…

The Magnis system provides a complete workflow for NGS library preparation that is fully automated and delivers reproducible results. Built on proven Agilent SureSelect XT HS2 chemistry, start from total RNA with integrated cDNA conversion or unfragmented DNA with onboard enzymatic fragmentation for increased workflow efficiency.

Targeted NGS library preparation, gene expression and genotyping. Increase productivity and efficiency with automated, cost-effective, and easy-to-use workflows for targeted DNA next-generation sequencing (NGS) library preparation, gene expression analysis and genotyping by allele-specific PCR.

Automated platform for single-cell omics and multi-omic research using solid-state microfluidics. C1 with integrated fluidic circuits (IFCs) enables the preparation of single-cell templates for total RNA sequencing and multi-omic applications such as preparing mRNA and DNA and mRNA and protein from the same isolated and imaged single cell.

SimpliFY Your Clean Ups. Microlab PuriFY offers a compact, standalone solution for automated nucleic acid bead-based clean-up for NGS library preparation and PCR, enabling scientists to spend less time of tedious, repetitive tasks and more time concentrating on their vital research.

Space-Saving, On-Deck Fluorescence Measurements. The Fluoreye mobile fluorescence reader is operated by a 1000 µL pipetting channel, moving to and measuring samples in 96-well flat-bottom plates.

Stop gambling on cycle numbers. The icon96 uses iconPCR™ technology with AutoNorm™ software to provide real-time fluorescence feedback in each of 96 independent wells, preventing under-amplification dropouts and over-amplification artifacts—delivering balanced, sequencing-ready libraries without manual quantification or normalization.

The new standard in benchtop sequencing speed and simplicity

Fast and Easy Library Workflows

Twist's RNA Sequencing Solutions provide comprehensive next-generation sequencing (NGS) workflows, offering both targeted and whole transcriptome approaches to generate uniform, high-quality RNA sequencing libraries from diverse sample types.