Related to Boosting Gene Expression Profiling

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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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• 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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• 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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• 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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• 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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• 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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• 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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• 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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• 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