Next Generation Sequencing Systems Products & Reviews

Exome sequencing has become a widely used practice in clinics and diagnostics. The superior performance of the Twist Human Core Exome provides the optimal solution for sequencing of protein coding genes, while focusing on the most accurate curated subset— CCDS database.

Illumina's MiSeq is the only fully integrated personal sequencer, delivering a streamlined solution that takes you from rapid sample prep through automated data analysis and storage in the BaseSpace cloud. Sequencing doesn’t get any easier than this. As the only personal sequencer capable of producing paired-end reads, Illumina's MiSeq system puts the largest portfolio of sequencing applications at your fingertips. Optimized…

Fast and affordable next-generation benchtop sequencer

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…

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 next level in diagnostic power for the clinical lab

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

Your new lab partner

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

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.

Power and efficiency for large-scale genomics. The HiSeq 2500 System features two run modes, rapid run and high output run mode, and the ability to process one or two flow cells simultaneously. This provides a flexible and scalable platform that supports the broadest range of applications and study sizes. No other system lets you perform so many applications so quickly and easily. Choose between rapid run and high output mode…

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…

Scale up your RNA extraction for SARS-CoV-2 research and detection

The NGSBIO Library Quant Kit contains all the components required for accurate and sensitive quantification of libraries prepared for for Illumina NGS systems.

The NGSBIO Library Quant Kit Blue contains all the components required for accurate and sensitive quantification of libraries prepared for Illumina NGS systems. The kit uses an easy-to-see blue qPCR mix to specifically quantify adapter-ligated DNA molecules, ensuring optimal cluster densities for improved sequencing efficiency and quality of data.

LiquidPlex panel is an advanced and user-friendly research assay for targeted next generation sequencing of circulating cell-free tumor DNA (ccfDNA/cfDNA/ctDNA) from 28 genes commonly associated with solid tumor type cancers.

FusionPlex Lung v2 is a research assay for targeted next generation sequencing of RNA for characterization of variants, indels, and fusions, including novel fusions, from 17 genes associated with NSCLC.

FusionPlex Core Solid Tumor is a research assay for targeted next generation sequencing of RNA for characterization of variants, indels, and fusions, including novel fusions, from 57 genes associated with various solid tumor malignancies.

FusionPlex Core Solid Tumor is a research assay for targeted next generation sequencing of RNA for characterization of variants, indels, and fusions, including novel fusions, from 57 genes associated with various solid tumor malignancies.