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Related to Solving the Next-Gen Sequencing Data Crunch

    • Scientific PDF Viewer
    • Utopia Documents
    • Utopia Documents v2.0 is a free PDF reader that connects scientific articles to online content. It allows link-outs to the web directly from highlighted text in a PDF to a range of data sources, scientific information, and semantic search tools. Us
    • NMR Software Tool
    • Bruker
    • CMC-assist™ is a software tool that provides routine NMR users with support in their daily workflow of spectral interpretation. CMC-assist can assign NMR signals to structural characteristics, conduct a structural consistency assessment, and provid
    • 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
    • Informatics Platform
    • PerkinElmer
    • The Ensemble® for Biology™ platform is an integrated informatics suite of applications for creating a collaborative and integrated biology workflow from research and development to quality assurance and control. This platform can help with dat
    • Liquid-Handling Software
    • Hamilton Company
    • Instinct is redesigned control software for the Microlab Nimbus automated liquid-handling workstation. Instinct supports a range of daily lab work with new tools that can simplify and streamline programming. A built-in labware library displays an i
    • 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
    • Genotyping Processor
    • SoftGenetics
    • GeneMarker MTP processes up to six varying chemistries or size standards in a single analysis run. Following the genotyping of the six projects, users have access to the applications found in GeneMarker software including MLPA®, MS-MLPA, Triso
    • Bioprocessing Software
    • Sartorius Stedim Biotech
    • BioPAT® MFCS/win functions as a true SCADA system for reusable and single-use bioprocess applications. The software package also makes it possible to trigger different actions automatically based on events (e.g., initialization of substrate fe
    • MS Data Analysis System
    • Genedata
    • Expressionist MSX® analyzes proteomics and metabolomics data for a variety of applications directly from the instrument. It can be downloaded in a Windows-executable file and can be set up in minutes. The algorithms in Expressionist MSX can re
    • Informatics Software
    • PerkinElmer
    • ChemBioOffice® informatics suite version 13.0 features improvements to the ChemBioDraw® and ChemBio3D® modules and provides cloud storage for data sharing. The ChemBioOffice suite can help chemists and biologists track their work and
    • 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
    • QA/QC Informatics Platform
    • PerkinElmer
    • The Ensemble® for QA/QC is an integrated informatics platform tailored to decrease procedural errors, and accelerate data review and results delivery of QA/QC laboratories. The platform utilizes a scalable architecture to support all levels of
    • Nitrocellulose Membranes
    • GE Healthcare Life Sciences
    • The Whatman™ FF High Performance (HP) membrane is a diagnostic membrane that enables line separation and reproducible results for the detection of target molecules in liquids such as water, urine, blood, and saliva. The target molecules may include
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GEN Poll

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Genome Sequencing and Patient Autonomy

Do you think ACMG’s recent recommendations for reporting incidental clinical sequencing results undermine patient autonomy?

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