DNA Sequencing Products & Reviews

The ABI PRISM® 310 Genetic Analyzer is an automated single-capillary genetic analyzer designed for a wide range of sequencing and fragment analysis applications. Perform comparative sequencing, linkage analysis, STR analysis, SNP detection, discovery and validation, mutation detection, and many other applications. Eliminate gel preparation. Set up runs in minutes. Automate your workflow to minimize hands-on time and costs. Det…

With the Applied Biosystems 3130 Genetic Analyzer, you get the sophisticated automation and superior performance of the 3130 system, at acquisition and operating costs tailored to a growing research lab. Run a wide variety of sequencing and fragment analysis applications including microsatellite analysis, AFLP, LOH, SNP validation, and SNP screening. Reduce maintenance time by eliminating manual syringe washing and filling wit…

Offering 16-capillary throughput and advanced automation capabilities, the Applied Biosystems 3130xl Genetic Analyzer is ideal for medium-throughput laboratories that need streamlined set-up and 24-hour unattended operation. Run a wide variety of sequencing and fragment analysis applications including microsatellite analysis, AFLP, LOH, SNP validation, and SNP screening. Reduce maintenance time by eliminating manual syringe wa…

The 96-capillary 3730xl DNA Analyzer is the Gold Standard for high throughput genetic analysis. Use this for DNA fragment analysis applications such as microsatellites, AFLP, SNP analysis, mutation detection and traditional DNA sequencing. Get the highest quality data at a low cost per sample. Higher optical sensitivity and advanced polymers enable you to obtain higher-quality sequencing data for less. Multiple automation feat…

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 Agencourt CleanSEQ system is a rapid, high performance dye-terminator removal process based on Solid Phase Reversible Immobilization (SPRI) technology.

Next-generation sequencing (NGS) technologies have dramatically reduced sequencing costs and led to novel approaches in many fields of biology.

The GS FLX Titanium emPCR Breaking Kit LV 12pc is used to break the emulsions and collect the beads from a single cup or up to a full day's worth of Large Volume Emulsion (LVE) Cups, providing they contain the same library. The kit contains components for 12 LV emulsion-breaking setups. Contents 12 pieces, each with one 8-channel transfer pipette, two 50 ml tube caps with tubing fittings, and tubing (approximately 1 meter in l…

OGT can help you get straight to the variant of interest with whole exome or custom targeted sequencing services. Genefficiency™ targeted sequencing services are designed to be different, leading you all the way from project conception to high-quality results. Our expert and comprehensive project design and analysis solutions — incorporating Agilent SureSelect, Illumina HiSeq 2000 and OGT-developed software platforms — are ta…

A high-quality RNA sequencing service designed to deliver cost-effective and rapid access to meaningful transcriptomics results. The Genefficiency™ RNA-Seq Service from OGT provides a new level of assay customisation to ensure each experiment is fully optimised to suit your specific study objectives. At OGT we understand the time and effort it takes to generate good quality RNA and how precious your samples are. Whether you a…

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…

Deliver sequencing data and results seamlessly without the need for local compute infrastructure. DNAnexus facilitates your management, analysis, and delivery of genomic data through a secure cloud platform that supports unlimited storage and computational resources. The sequence data your facility produces is sent to the DNAnexus platform with our automated uploader tool, integrated with your LIMS. A single high-bandwidth co…

The SageELF is an automated, whole-sample fractionation system for NGS sample prep. SageELF, a whole-sample fractionation tool, is now shipping from Sage Science, developer of the Pippin automated DNA size selection system. The SageELF (short for Electrophoretic Lateral Fractionator) generates 12 contiguous fractions from a whole DNA sample, allowing scientists to generate libraries with multiple insert sizes from the same sa…

If you meet these needs: PCR and sequencing clean-up gDNA from various matrixes Plasmid preparation General liquid handling tasks Forensics Sequencing setup Sample preparation for LC-MS/MS analysis PrimaDiag offers ACSIA CleanUp Edition. With the aim to increase your productivity, avoid contamination and improve work efficiency, PrimaDiag designed ACSIA CleanUp Edition. It is a compact and robust automated pipe…

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…

ACSIA NGSLibPrep Edition, the solution to automate the libraries preparation for next-generation sequencing. In view of increasing your productivity, avoiding contamination and improving your work efficiency, PrimaDiag created ACSIA NGSLibPrep Edition. It uses our software PrimaControlleur®II and has been designed to allow you to effectively perform your libraries preparation.ACSIA NGSLibPrep Edition allows you to perform 96…

Discover the diversity of microbial communities

SUPREMERUN is optimised for Sanger sequencing of your individual research samples in tubes or 96 well plates. 

LIGHTRUN is our most convenient Sanger sequencing solution for your premixed samples.

Highlights: Fastest exome sequencing, starting from one sample Applicable for genomic DNA from various sources (tissue, cells, blood and FFPE sample) Special protocol for low-input samples (≥ 10ng) Available under diagnostics standard (ISO17025) INVIEW™ stands for streamlined high-quality next generation sequencing (NGS) solutions for specific applications. Exome enrichment with the latest Agilent SureSele…

An unprecedented view into transcriptional heterogeneity

New insights from beyond the sequence

Revolutionary, cost-effective genome assembly

Source BioScience are one of Europe’s leading providers of commercial sequencing offering services on the most prominent next generation sequencing platforms including the Illumina MiSeq and HiSeq. Source BioScience's next generation sequencing service is Illumina CSPro accredited and operates through a robust quality management system. Customers benefit from both excellent service and rapid turnaround times. Source BioScienc…

Protein Analysis Software - the Next GenerationCLC Protein Workbench creates a software environment enabling users to make a large number of advanced protein sequence analyses, combined with smooth data management, and excellent graphical viewing and output options. Protein Workbench sets new standards for bioinformatics software with its overall graphical display, usability driven and user-friendly interface, while featuring…