Next Generation Sequencing Products & Reviews

The Sciclone™ G3 NGSx workstation is a complete benchtop solution for the automated construction of up to or greater than 96 libraries per day. For Research Use Only. Not for use in diagnostic procedures.

Biomek Liquid Handlers enable you can spend less time on manual process and more time on powerful discoveries. Beckman Coulter Life Sciences is a leader when it comes to providing solutions and support that cover the full spectrum of the NGS sample preparation workflow with reagents and automation. Throughput options allow you to choose the right solution for your laboratory.

The NEBNext® Ultra™ Directional RNA Library Prep Kit for Illumina® contains enzymes and buffers that are ideally suited for cDNA library preparation for next-generation sequencing. NEBNext® reagents are a series of highly pure reagents that facilitate sample preparation of DNA or RNA for downstream applications such as next generation sequencing and expression library construction. The reagents included within these master mi…

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…

Dominating the high-throughput sequencing data analysis challenge We have overcome the challenge to analyze high-throughput sequencing data faster than it is produced by implementing a SIMD-accelerated assembly algorithm in our next generation sequencing solution, CLC Genomics Workbench – a cross-platform desktop application with a graphical user-interface. CLC Genomics Workbench, for analyzing and visualizing next generation…

ACSIA NGSCapture Edition, the solution to automate the steps of library preparation and, more specifically, of target enrichment. ACSIA NGSCapture Edition allows you to perform 48 samples without human intervention or 96 samples with one intervention during the enrichment step. To do so, it operates from just after the hybridization up through the final PCR amplification. It is in this last step at the end of the process that…

SMART-Seq v4 Ultra Low Input RNA Kit for Sequencing—Single-Cell Transcriptome Analysis with Ultimate Sensitivity

The New Standard for Desktop-Based Bioinformatics Tools CLC DNA Workbench provides a software environment which enables users to perform advanced DNA sequence analyses such as assembly of DNA sequence data, graphically and algorithmically advanced primer design, while offering user-friendly molecular cloning tools. CLC DNA Workbench is a bioinformatics software package containing a range of specialized DNA analyses and bioinfo…

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 Eurofins sequencing services provide you with the most flexibility for your samples in tubes and plates. Tube Sequencing Services Mix2Seq TubeSeq Service TubeSeq Lables Ready2Load Plate Sequencing Services PlateSeq Service PlateSeq Kits Ready2Load Plate Get your Mix2Seq Kit to benefit from the smartest sequencing solution for your DNA samples premixed with primer. Available as overnight and Non-overnigh…

Exceptional Gene Silencing Specificity For Reliable Phenotypes

The SureCell ATAC-Seq Library Prep Kit and ATAC-Seq Analysis Toolkit enable reproducible genome-wide profiling of the epigenomic landscape at the single-cell level with a high number of unique reads per cell so you can better understand the mechanisms that drive how genes are regulated. Features and Benefits Greater than 65% and up to 95% cell capture efficiency Adjustable cell throughput range of as few as…

End-to-end transcriptome sequencing services from RNA extraction to sequencing to bioinformatic analyses.

Eton provides the following sequencing services tailored to your specific research.

CD Genomics provides complete plasmid DNA sequencing service, and their improved bioinformatics pipelines are available to perform de novo assembly with no reference required.

VAHTS TM  DNA Clean Beads are based on the SPRI (Solid Phase Reverse Immobilization) principle and are suitable for DNA purification and fragment size sorting in the construction of high-throughput sequencing libraries. VAHTS TM DNA Clean Beads are compatible with various brands of DNA and RNA library building kits and the library building process reported in the literature. 

Get the most complete genomic information of any organism with whole genome sequencing (WGS). Macrogen Europe’s fast, high-quality WGS services provide the most comprehensive tool for detecting genetic abnormalities such as single nucleotide polymorphisms (SNPs), indels, copy number variation (CNV) and structural variants (SVs).

The NEBNext Ultra II FS DNA PCR-free Library Prep Kit for Illumina offers an amplification-free workflow for DNA-seq based on the streamlined and reliable Ultra II FS workflow. Starting with as little as 50 ng of DNA, get the high-quality, high-yield libraries that you need without PCR bias.

Economical 2-component kit ideally suited for high throughput gene-expression studies

mRNA sequencing (mRNA-seq) is a potent method for gene expression exploration, it unveils mRNA dynamics, different gene expression and regulatory mechanisms with precision.

Achieve new levels of automation performance with the Thermo Scientific™ Momentum™ Workflow Scheduling software-  an industry-leading software platform that enables users to define, execute, and monitor scientific processes and workflows in a powerful yet easy-to-use visual environment. Its intuitive scheduling interface, intelligent data-driven decision-making capabilities, superior connectivity and flexible simulation modes…

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…

Kit for determining the nucleotide sequence (in extra-long reads, up to 1kb) of an immobilized and clonally amplified DNA library prepared using the GS FLX+ System methods for the preparation of DNA libraries and amplified by the emPCR amplification process, using the appropriate GS FLX Titanium series kit(s). For use in combination with the GS FLX Titanium PicoTiterPlate Kit 70 × 75 and the GS FLX+ Instrument. Contents The GS…

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…