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Related to Novel Systems Zero In on the $100 Genome

    • Next-Gen Sequencing Software
    • Interactive Biosoftware
    • Alamut HT is a human genomic variation annotation and interpretation solution. As a high-throughput annotation engine for next-generation sequencing (NGS), it is designed for intensive variant analysis workflows. This software enriches raw NGS vari
    • Sequencing Assays
    • Roche
    • GS GType TET2/CBL/KRAS and the GS GType RUNX1 primer sets are designed for comprehensive genetic variation detection in four key human genes using the 454 GS Junior and GS FLX Systems. The sequence-based assays offer a solution for cancer researche
    • DNA Fragment Analysis
    • Advanced Analytical
    • The new Fragment Analyzer™ can provide a high-throughput alternative to lab-on-a-chip methods for qualifying DNA fragments prior to next-gen sequencing runs. The Fragment Analyzer can help labs under pressure from increasing sample workloads. No fl
    • Capture Oligonucleotides
    • Integrated DNA Technologies (IDT)
    • xGen™ Lockdown™ probes are individually synthesized 60–120 nucleotide 5’-biotinylated capture oligonucleotides designed to enable high-depth sequencing and analysis of specific regions of the genome. xGen Lockdown probes work well for target enrich
    • DNA Library Prep
    • New England BioLabs
    • The NEBNext® Ultra DNA Library Prep Kit for Illumina® contains enzymes and buffers that can convert a small amount of DNA input into indexed libraries for next-generation sequencing on the Illumina platform. The workflow of NEBNext Ultra
    • Sequencing System
    • Roche
    • The GS FLX+ system performs applications including de novo sequencing, resequencing of whole genomes and target DNA regions, metagenomics, RNA analysis, and ultra-deep amplicon sequencing. This system can deliver one million reads with an accuracy
    • Target-Enrichment Reagent Kits
    • Roche
    • SeqCap EZ reagent kits are used for application in single or multiplex target-enrichment experiments prior to DNA sequencing. Designed to streamline the DNA preparation workflow, the kits can provide customers with a reagent solution for use in tar
    • NGS Sample Prep Library Kit
    • Swift Biosciences
    • The Accel-NGS™ DNA library kit is the first product in a new line of kits for next-generation sequencing sample preparation. Users can produce PCR-free libraries with 5 Ng of input DNA. The two-step adaptation process also reduces adapter dimer for
    • Sequencing System
    • Pacific Biosciences
    • The PacBio RS II allows scientists to generate finished genome assemblies, reveal and understand epigenomes, and characterize genomic variation. Based on the SMRT sequencing technology, the RS II can generate average read lengths of 5,000 base pair
    • Library Quantification Kit
    • Bio-Rad
    • Used with the QX100™ Droplet Digital™ PCR system, the ddPCR™ library quantification kit lets researchers directly measure amplifiable library concentrations. The TruSeq sample preparation method is the technique behind Illumina’s MiSeq and HiSeq ne
    • LIMS for NGS
    • GenoLogics Life Sciences Software
    • Specifically designed for sequencing, Clarity LIMS is a lab management system that combines information management essentials for CLIA-certified and regulated labs with an easy-to-navigate interface. Clarity LIMS can offer support for clinical lab
    • mRNA Kit for Next-Generation Sequencing
    • IntegenX
    • A directional messenger RNA (mRNA) kit is now available for automated NGS library preparation on the Apollo 324T System. Co-developed with New England Biolabs and requiring just 500 picograms of mRNA starting material, the PrepX RNA-Seq library pre
    • Exome Sample Prep
    • Agilent Technologies
    • SureSelect Human All-Exon V5 and V5 + UTRs for next-generation sequencing produce exome samples ready for sequencing the next day. They also provide good sequencing efficiencies as well as coverage of current genomics databases including RefSeq, CC
    • NGS Fragment Library Prep
    • Beckman Coulter
    • SPRIselect utilizes SPRI (Solid Phase Reversible Immobilization)-based chemistry to simplify genomic DNA size selection for next-generation sequencing fragment library preparation. Following shearing, the library construction process requires size
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