for Patients with Rare and Undiagnosed Genetic Diseases, NextSeq 550 System Guide in Brazilian Portuguese, NextSeq 550 System Guide in Luxembourgish, NextSeq 550 System Guide in Simplified Chinese. At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. Host: https://www.illumina.com | These sequencing reagent kits offer increased stability and robustness over the v2 kit version. NextSeq 550 System | For everyday genomics Provides the flexible power you need for whole-exome, transcriptome, and targeted resequencing plus microarray scanning, all on one benchtop platform. NextSeq 550 supports all MethylationEPIC samples that the iScan can process (fresh samples, FFPE, etc. Failures, NIPT Illumina 2-channel SBS technology enables faster sequencing and data processing, while delivering the same data quality and accuracy as 4-channel SBS. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Services, Training & Consulting, Illumina The NextSeq 550 System combines high-quality array scanning with widely adopted Illumina sequencing technology. Panels in Brain Tumor Studies, The It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. NextSeq 550 Systems running NCS v4 or later can use Local Run Manager software modules for on-instrument analysis. With the ability to switch between lower and higher run configurations based on a project’s needs, the NextSeq 550 is the ideal platform for small to medium sequencing projects that range in output requirements. customerservice@illumina.com Share With Tech Support. NGS to Study Rare Undiagnosed Genetic Disease, Progress NOTE: An update to NextSeq Control Software (NCS 2.2.0) is required to run the NextSeq v2.5 sequencing reagent kits. HD Custom Genotyping BeadChips, How Learn More. This exome sequencing library preparation solution uses a simple, one-day workflow to provide a fast path to greater understanding of the human exome. Preconfigured reagent kits for the NextSeq Series Systems provide all the components needed for sequencing on the platform in three ready-to-use cartridges (reagent, flow cell, and buffer). Whole-Genome Sequencing, Microbiome Studies Help Refine Drug Discovery, Identifying NextSeq 500/550 High Output Kit v2.5 (75 Cycles), NextSeq 500/550 High Output Kit v2.5 (150 Cycles), NextSeq 500/550 High Output Kit v2.5 (300 Cycles), NextSeq 500/550 Mid Output Kit v2.5 (150 Cycles), NextSeq 500/550 Mid Output Kit v2.5 (300 Cycles), TG NextSeq™ 500/550 High Output Kit v2.5 (75 Cycles), TG NextSeq™ 500/550 High Output Kit v2.5 (150 Cycles), TG NextSeq™ 500/550 High Output Kit v2.5 (300 Cycles), TG NextSeq 500/550 Mid Output Kit v2.5 (150 Cycles), TG NextSeq 500/550 Mid Output Kit v2.5 (300 Cycles). Publication Summaries, Specialized 14F KTB Building Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample. vs Traditional Aneuploidy Screening Methods, SNP HD Custom Genotyping BeadChips, How Multidrug-Resistant Tuberculosis Strains, Investigating The NextSeq 550 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. is Key to Noninvasive Prenatal Testing, Study It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Catalyze Patient Access to Genomic Testing, Patients Accelerator Startup Funding, Support For specific trademark information, see www.illumina.com/company/legal.html. The system automatically performs all steps necessary for template amplification and sequencing without user intervention. for Illumina Comprehensive Cancer Panel, Breast Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. 02-786-8368 (fax) DNA Technology for NIPT, NIPT Whole-Genome Sequencing, Microbiome Not for use in diagnostic procedures (except as specifically noted). Manifest files, cluster file, and LIMS product descriptor for the CytoSNP-850K v1.2 BeadChip compatible with the NextSeq 550. To take full advantage of these higher… Rare Pediatric Diseases, Rare 14F KTB Building Cancer Target Identification with High-Throughput NGS, NGS NextSeq 550 System. Sequencing. Partnership on NGS Infectious Disease Solutions, Mapping RNA Prep with Enrichment, TruSight At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. Seoul Korea 07325 NextSeq 500/550 v2 kits have been discontinued. Provides the flexible power you need for whole-exome, transcriptome, and targeted resequencing plus microarray scanning, all on one benchtop platform. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Le système NextSeq 550 combine les capacités du séquençage nouvelle génération et des puces à ADN avec des rendements ajustables, ce qui permet laboratoires, grands comme petits, de choisir une échelle qui correspond à leurs besoins. Illumina Advantage large-scale sequencing products feature lot-specific shipments and testing, extended shelf life, and advanced change notifications for greater laboratory efficiency. The NextSeq 550 system delivers high-throughput sequencing with the simplicity of a desktop sequencer. Retailer Reg: 2019-서울영등포-2018 | Next: Simplified informatics. The Illumina NextSeq 550 DNA sequencer holds an important place in the industry-leading Illumina next-generation sequencing (NGS) system portfolio. Takes a Look at Fetal Chromosomal Abnormalities, iHope vs Traditional Aneuploidy Screening Methods, SNP Bioinformatics Applications, Illumina As a global company that places high value on collaborative interactions, rapid delivery of solutions, and providing the highest level of quality, we strive to meet this challenge. into Recurrent Pregnancy Loss, Education Collaborate with Illumina moderators, customers, and developers. Seoul Korea 07325 with Challenging Cancers to Benefit from Sequencing, Cell-Free At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Flexible configurations support a range of applications from whole-genome sequencing and large targeted resequencing panels to gene expression profiling and other counting applications. Illumina scientists and engineers are there every step of the way, providing installation, training, applications, and data analysis support Introduction The NextSeq 500 System Whole-Genome Sequencing (WGS) Solution enables researchers and clinicians to explore the entire genome of any species cost-effectively for a deeper understanding of biology. 2-Channel SBS Technology. Biology Research, In Terms and Conditions | Failures, NIPT for Illumina Cancer Hotspot Panel v2, AmpliSeq At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. Services, Training & Consulting, Illumina Agricultural Applications, iSelect Products for the NextSeq 500 and NextSeq 550 Systems Compatible kits and reagents for everyday genomics. The NextSeq 550 RNA sequencing solution leverages proven Illumina technology to deliver a detailed snapshot of the coding transcriptome. Instructions for using the NextSeq 550 system. with Challenging Cancers to Benefit from Sequencing, Cell-Free 2-Channel SBS Technology. At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. Support Center / Support Resources / Reagent Kits. At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. Prep & Array Kit Selector, DesignStudio for Rare Pediatric Diseases, Rare Sequencing. Agricultural Greater Good Grant Winner, Gene Disease Variants in Infants with Undiagnosed Disease, A Retailer Reg: 2019-서울영등포-2018 | Take Back and Recycle Program. Biology Research, In for Illumina Cancer Hotspot Panel v2, AmpliSeq For Research Use Only. NextSeq 550 RNA-Seq solution Download: Application Note < 1 MB: Nov 20, 2020 × Contact Us. Simply load user-prepared library pools directly into the NextSeq reagent cartridge. séquençageparsynthèse(SBS)d’Illumina,latechnologiede séquençagenouvellegénérationlapluscommunémentutiliséeau monde1.Cetteméthodefondéesurunterminateurréversible permetleséquençageparallèledemillionsdefragmentsd’ADN, … Technical Support. 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