Related to mRNA Kit for Next-Generation Sequencing

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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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• 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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• DNA Polymerase
• New England BioLabs
• The Q5™ high-fidelity DNA polymerase can provide high- fidelity amplification while also offering amplification across a range of amplicons, including those that are GC- and AT-rich. This polymerase is fused to the processivity-enhancing Sso7d DNA
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• 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
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• 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
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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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• 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
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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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• Sequence Analysis Software
• DNASTAR
• Lasergene 10 is a Sanger and next-generation sequence analysis and assembly software upgrade with new features to its desktop software suite for molecular biologists. Among other changes, Lasergene 10 introduces SeqNinja, a tool for manipulating an
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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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• 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