Related to Future of DNA Sequencing Technology

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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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• ssDNA Quantitation
• Promega
• The QuantiFluor™ ssDNA system is designed for highly sensitive quantitation of single-stranded DNA (ssDNA). The QuantiFluor ssDNA dye enables quantitation of small amounts (as little as 200 pg per well) of ssDNA in solution. For low-concentration s
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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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• Genome Mapping System
• BioNano Genomics
• The Irys™ is a genome mapping system that can help genomics researchers with structural variation analysis and sequence assemblies. Irys is an automated platform that uses single-molecule imaging to visualize extremely long nucleic acids and reveal
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• Genetic Analyzer
• Pacific Biosciences
• The PacBio® RS high-resolution genetic analyzer has undergone a software upgrade featuring additional tools for performing DNA base modification analysis and de novo genome assembly. With the release of the SMRT Analysis 1.3.3 software upgrade
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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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• 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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• 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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• Sample Quality Control
• Agilent Technologies
• The Genomic DNA ScreenTape can work with the 2200 TapeStation instrument to determine the quantity, size, and quality of genomic DNA in less than two minutes per sample, using only one microliter of material. This automated sample QC tool can be us
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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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• Bisulfite Conversion System
• Promega
• The MethylEdge™ bisulfite system offers a method for performing bisulfite conversion and DNA clean-up while maintaining DNA integrity to provide intact, converted DNA for a range of sensitive applications. MethylEdge requires small amounts of input
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• Plant and Seed DNA Isolation Kits
• Mo Bio Laboratories
• Two new kits are available with Inhibitor Removal Technology to remove polysaccharides, polyphenolics, and lipids for pure DNA. The PowerPlant Pro-htp 96-Well Kit enables high-throughput isolation of pure DNA from plants and seeds in a 96-well form
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• Genetic Variant Annotation Software
• BIOBASE Biological Databases
• Annovar® is a command-line tool that uses information to functionally annotate genetic variants from high-throughput sequencing data detected from different genomes (including human genome hg18, hg19, as well as mouse, worm, fly, yeast, and ot
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• Stabilized Pepsin
• SciGene
• CytoZyme™ stabilized pepsin is an advanced formulation for pretreating tissue samples in nucleic acid probe-based cytogenetic assays including FISH. CytoZyme is a ready-to-use solution of purified pepsin that can be stored in the refrigerator witho
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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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• 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
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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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• 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