Related to NGS & RNA-Seq Form Dynamic Duo

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• 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
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• 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
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• Gene-Editing Services
• Cellectis bioresearch
• Custom TALEN™ services can help researchers with gene-editing projects including gene knockout, gene tagging, promoter swapping, and nucleotide substitution. Project support managers can provide users with expertise to achieve customized cells and
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• RNA-Seq Library Prep
• Epicentre Biotechnologies
• ScriptSeq™ Complete Kits combine Ribo-Zero™ technology and ScriptSeq v2 method for end-to-end preparation of directional RNA-Seq libraries in one day. The ScriptSeq Complete Kits use 1–5 μg of total RNA, and the ScriptSeq Complete Kits—Low Input us
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• 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
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• Tumor Marker Control
• Randox Laboratories
• The Acusera multianalyte liquid tumor marker control covers a total of 15 commonly tested and esoteric cancer antigens and tumor markers. Assayed target values can help laboratories monitor both accuracy and precision. The liquid stable nature redu
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• Gene-Expression Microarray
• Agilent Technologies
• The SurePrint G3 Human Gene-Expression v2 microarray is available with an array of probes designed using the Broad Institute’s human reference catalog of large intergenic noncoding RNAs. The microarray is part of a microarray platform with a range
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• BRAF Mutation Detection
• Swift Biosciences
• myT BRAF-Ultra, an ultrasensitive version of myT BRAF, provides 0.01% sensitivity down to single-copy detection of BRAF mutations. myT BRAF-Ultra can detect less than 10 copies of mutant BRAF V600E/K with low breakthrough amplification from a backg
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• Single-Cell Gene Expression Assay
• NanoString Technologies
• A single-cell gene expression application is now available that can provide researchers with a flexible and sensitive approach to discovering differences in cell-to-cell gene expression profiles. The nCounter® Single-Cell Gene Expression assay
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• 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
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• Cell-Line Customization Service
• Cellectis bioresearch
• Gene customization experts can modify cell lines at any gene, at any position. Services available include gene modification, knock-out, and targeted transgene integration. Thirteen years of genome customization expertise, TALEN™ technology, and IP
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• 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
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• 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
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• 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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• mRNA Sequencing
• Fluidigm
• The C 1 Single-Cell Auto Prep system now features an mRNA sequencing application that can give researchers an end-to-end workflow for transcriptome analysis of 96 single cells. mRNA Seq kits and integrated fluidic circuits enable the parallel proce
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• 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
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• Knockout Cell Lines for Cancer Research
• Cellectis bioresearch
• The cells in CanCELL™ cell lines represent comprehensive knockouts of major disease-relevant oncogenes and tumor suppressor genes. CanCELL cell lines are generated using TALEN™ technology and offer opportunities to study signaling pathways and gene
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• Transfection Reagent
• Mirus Bio
• TransIT®-BrCa transfection reagent is a dedicated breast cancer cell-line specific reagent that can help researchers achieve high expression levels in breast cancer cell types including MCF-7, MDA-MB-231, MDA-MB-453, MDA-MB-468, and T47D. It c
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• DNA Reference Standard
• Horizon Discovery
• The Quantitative Multiplex DNA reference standard is intended for researchers assessing multiple biomarkers in a single assay using platforms such as next-generation sequencing. It can enable researchers to quantify a range of detection thresholds
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• 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