Next-generation sequencing (NGS), also known as whole-genome sequencing, high-throughput sequencing and massive parallel sequencing, produces and analyses thousands to millions of nucleotide sequences at once. Sequencing systems operate via varying technologies depending on the manufacturer, including sequencing by synthesis, ligation, pyrosequencing, ion semiconductor and single-molecule real-time sequencing. For NGS, library preparation is paramount to successful sequencing. In this section, explore a range of library preparation kits, from targeted, amplicon-based or hybridization-based kits including epigenomic, transcriptomic and genomic workflows to fragmentation kits. Find the best next-generation sequencing products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.
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…
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
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…
