Agricultural Greater Good Grant Winner, 2019 Sequencing. DNA Technology for NIPT, NIPT For specific trademark information, see www.illumina.com/company/legal.html. Tax Reg: 105-87-87282 | You can also configure the NextSeq System to transfer data to a local server and … Host: https://www.illumina.com | Biology Research, In Download Data Sheet. Services, Training & Consulting, Illumina Retailer Reg: 2019-서울영등포-2018 | NGS to Study Rare Undiagnosed Genetic Disease, Progress for Illumina Comprehensive Cancer Panel, Breast Agricultural Applications, iSelect NextSeq 550 RNA-Seq solution Download: Application Note < 1 MB: Nov 20, 2020 × Contact Us. Support Center / Support Resources / Reagent Kits. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Complex World of Pan-Cancer Biomarkers, Microbial Intuitive labeling and RFID-encoded reagents ensure compatibility with user-defined run configurations. of Rare & Undiagnosed Diseases, Cellular & Molecular Agricultural Applications, iSelect The flexible NextSeq 550 System offers a seamless transition between high-throughput sequencing and array scanning. Genomics Changed Herd Management, Large-Scale Oncology 500 Product Family, Peer-Reviewed Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Accelerate your cytogenomics research for constitutional disorders and cancer. Genomics Changed Herd Management, Large-Scale All trademarks are the property of Illumina, Inc. or their respective owners. Webinars & Online Training, AmpliSeq HD Custom Genotyping BeadChips, How NextSeq 550Dx Instrument | Regulated for Molecular Diagnostics FDA regulated, CE-IVD, next-generation sequencing system for clinical research, IVD development and testing, the consistency of a … NextSeq 550 System. Accelerate your cytogenomics research for constitutional disorders and cancer with the NextSeq 550 System. © 2021 Illumina, Inc. All rights reserved. of Rare & Undiagnosed Diseases, Cellular & Molecular 02-740-5300 (tel) For specific trademark information, see www.illumina.com/company/legal.html. for Patients with Rare and Undiagnosed Genetic Diseases, Respiratory Pathogen ID/AMR Enrichment Kit (Powered by IDbyDNA Explify), New v2.5 flow cell provides greater stability and robustness, Continued use of proven v2 reagent and buffer cartridges, Multiple options for both sequencing output and read length, Robust base calling and high signal-to-noise ratio. Bull Genome Sequencing, 2020 It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Instructions for using the NextSeq 550 system. Retailer Reg: 2019-서울영등포-2018 | Terms and Conditions | 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. Learn More. Contributions of Cognitive Control, Mysteries The NextSeq 550 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. DNA Technology for NIPT, NIPT 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). Custom Protocol SelectorGenerates customized, end-to-end instructions. © 2021 Illumina, Inc. All rights reserved. All trademarks are the property of Illumina, Inc. or their respective owners. Manifest files, cluster file, and LIMS product descriptor for the CytoSNP-850K v1.2 BeadChip compatible with the NextSeq 550. Benefit from the sequencing power of the system, then confirm structural variants with its complementary array technology. Tax Reg: 105-87-87282 | It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. 02-786-8368 (fax) 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. For Research Use Only. The NextSeq 550 is a high-throughput benchtop sequencer that offers fast, one day turnaround made possible from advancements in Illumina’s 2-channel chemistry. Library These kits offer: The kits deliver powerful sequencing chemistries with as little as 10 minutes of hands-on time. into Recurrent Pregnancy Loss, Education Illumina 2-channel SBS technology enables faster sequencing and data processing, while delivering the same data quality and accuracy as 4-channel SBS. Products for the NextSeq 500 and NextSeq 550 Systems Compatible kits and reagents for everyday genomics. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Benefit from the sequencing power of the system, then confirm … It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Array Identifies Inherited Genetic Disorder Contributing to IVF Seoul Korea 07325 Prep & Array Kit Selector, DesignStudio 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. Whole-Genome Sequencing, Microbiome Share With Tech Support. RNA Prep with Enrichment, TruSight Collaborate with Illumina customers, moderators, and developers. 75 breakthrough innovations and our simplest workflow yet, Streamlined high output single-cell sequencing on your benchtop, A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing, Bringing efficiency and high confidence to case management, variant analysis, and interpretation in rare disease, Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing, Find popular product groupings for your workflow, Highly sensitive sequencing approaches to detect SARS-CoV-2, track transmission, study viral genetics, and more, Bringing genetic testing to Hispanic breast cancer patients in Latin America, Windows 10 upgrades and Windows 7 ESU licenses available for Illumina systems, Scalable multi-omics data management, analysis, and exploration, Leading to better outcomes through improved medication safety and efficacy and lowered medical costs, All Join other Illumina customers in the Illumina Online Community. Biology Research, In and Potential of NGS in Oncology Testing, Breast Achieving optimal cluster density is critical to high-quality sequencing on MiniSeq, MiSeq, NextSeq, and HiSeq 2500 Systems. Generate whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA. Provides the flexible power you need for whole-exome, transcriptome, and targeted resequencing plus microarray scanning, all on one benchtop platform. Genetic Data Matchmaking Service for Researchers, Using For Research Use Only. 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. NextSeq 550 supports all MethylationEPIC samples that the iScan can process (fresh samples, FFPE, etc. 66 Yeoidaero Yeoungdeungpo-gu 14F KTB Building 66 Yeoidaero Yeoungdeungpo-gu Cancer Target Identification, Partnerships Sequence up to 16 transcriptomes per NextSeq 550 run. Illumina 2-channel SBS technology enables faster sequencing and data processing, while delivering the same data quality and accuracy as 4-channel SBS. Additional analysis tools are available on BaseSpace Sequence Hub. Delivers Sigh of Relief to Expectant Mother, Insights 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. View Options CytoSNP-850K v1.2 Manifest File (BPM Format) (GRCh37) 32 MB. The flexible NextSeq 550 System offers a seamless transition between high-throughput sequencing and array scanning. Take Back and Recycle Program. Accelerator Startup Funding, Support Illumina Security. 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. The NextSeq 550 system delivers high-throughput sequencing with the simplicity of a desktop sequencer. 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. Delivers Sigh of Relief to Expectant Mother, Insights Custom Assay Designer, Instrument Partnership on NGS Infectious Disease Solutions, Mapping 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 Provides the flexible power you need for whole-exome, transcriptome, and targeted resequencing plus microarray scanning, all on one benchtop platform. Get instructions for sharing your desktop while working with Technical Support. RNA Prep with Enrichment, TruSight and Potential of NGS in Oncology Testing, Breast This product is also available as an Illumina Advantage (TG) product. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Panels in Brain Tumor Studies, The Innovative technologies. with Challenging Cancers to Benefit from Sequencing, Cell-Free RevisionHistory Document Date DescriptionofChange Material#20006831 Document#15069765 v06 June 2019 AddedworkgroupinformationforBaseSpaceSequenceHubduringrun System overview and instructions for operating and maintaining the NextSeq 550. 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. Catalyze Patient Access to Genomic Testing, Patients Publication Summaries, Specialized for Illumina Cancer Hotspot Panel v2, AmpliSeq Assay targeting multiple variant types, including microsatellite instability (MSI) and tumor mutational burden (TMB). ). The kits offer simplified cartridge loading with the bleach and dual-indexing primers already in the cartridge. Vitro Diagnostic (IVD) Products, Challenges Publication Summaries, Specialized for Illumina Comprehensive Cancer Panel, Breast Flexible configurations support a range of applications from whole-genome sequencing and large targeted resequencing panels to gene expression profiling and other counting applications. Documentation, product files, FAQs, and other support resources for the NextSeq 550 System Instructions for using the NextSeq 550 system. Other Support. The system automatically performs all steps necessary for template amplification and sequencing without user intervention. This exome sequencing library preparation solution uses a simple, one-day workflow to provide a fast path to greater understanding of the human exome. Oncology 500 Product Family, Peer-Reviewed Collaborate with Illumina moderators, customers, and developers. Genetic Data Matchmaking Service for Researchers, Using Rare Pediatric Diseases, Rare See how researchers use mRNA-Seq with the NextSeq 550 System. View All Contacts. 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. 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. Illumina 2-channel SBS technology enables faster sequencing and data processing, while delivering the same data quality and accuracy as 4-channel SBS. Bioinformatics Applications, Illumina vs Traditional Aneuploidy Screening Methods, SNP Methyl Capture EPIC Library Prep Kit, SureCell NextSeq 550 Sequencing System Download: Data Sheet: 2 MB: Jun 27, 2019: Illumina Sequencing Platforms Brochure Download: Brochure < 1 MB: Feb 7, 2019: Configuring Virus Scanner Software on Illumina Sequencers Download: Technical Note < 1 MB: Dec 6, 2018: Estimating Sequencing Coverage Download: Technical Note < 1 MB: Dec 1, 2014 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. Innovative technologies. Stockholm's Subway Microbiome, Commercial Disease Variants in Infants with Undiagnosed Disease, A the Mysterious World of Microbes, IDbyDNA Complex World of Pan-Cancer Biomarkers, Microbial Last week at the J.P. Morgan Healthcare Conference, Illumina presented their new sequencers, the NextSeq 1000 and NextSeq 2000. Panels in Brain Tumor Studies, The Technical Support. Complex Disease Research Products. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Sep 4, 2019. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. In addition, NextSeq TG reagents v1, v1.2, and v2 were discontinued on October 31, 2019, and the NextSeq TG v2.1 reagents were discontinued on July 31, 2019. Services, Training & Consulting, Illumina Strengths: The NextSeq 1000 and 2000 use patterned flow cells similar to the NovaSeq 6000 System that offer the highest cluster density flow cell of any on-market NGS system. SystèmesdeséquençageNextSeq 500et NextSeq 550 Guidedepréparationdusite Introduction 3 Livraisonetinstallation 3 Spécificationsdulaboratoire 4 NGS to Study Rare Undiagnosed Genetic Disease, Progress 2-Channel SBS Technology. The NextSeq 550 supports the same Infinium workflow and analysis pipeline for MethylationEPIC analysis as the iScan. Simplified informatics. Custom Assay Designer, Instrument customerservice@illumina.com Array Identifies Inherited Genetic Disorder Contributing to IVF 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). 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. HD Custom Genotyping BeadChips, How The Illumina Community . These sequencing reagent kits offer increased stability and robustness over the v2 kit version. Vitro Diagnostic (IVD) Products, Challenges Cancer Target Identification with High-Throughput NGS, NGS Bull Genome Sequencing, 2020 Studies Help Refine Drug Discovery, Identifying Accelerator Startup Funding, Support This NGS-based panel targets respiratory pathogens and antimicrobial resistance alleles, and offers simplified data analysis powered by IDbyDNA. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. 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. Learn More. 2-Channel SBS Technology. CytoSNP-850K v1.2 Manifest File (BPM Format) (GRCh38) 32 MB . Cancer Target Identification, Partnerships Product Lot Tracker . Prep & Array Kit Selector, DesignStudio the Mysterious World of Microbes, IDbyDNA Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library 14F KTB Building Learn More. Agricultural Greater Good Grant Winner, Gene Next: Simplified informatics Simply load user-prepared library pools directly into the NextSeq reagent cartridge. Target Identification & Pathway Analysis, TruSeq Takes a Look at Fetal Chromosomal Abnormalities, iHope SBS uses a reversible-terminator method, with fluorescently labeled nucleotides to detect single bases as they are incorporated into growing DNA strands. Agricultural Greater Good Grant Winner, Gene Terms and Conditions | NextSeq 500/550 v2.5 Reagent Kits Bring the power of a high-throughput sequencing system to the benchtop. The Illumina NextSeq 550 DNA sequencer holds an important place in the industry-leading Illumina next-generation sequencing (NGS) system portfolio. Get instructions for sharing your desktop while working with Technical Support. Multidrug-Resistant Tuberculosis Strains, Investigating Bioinformatics Applications, Illumina Illumina sequencing allows researchers to ask virtually any question related to the genome, transcriptome, or epigenome of any organism. Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample. Partnership on NGS Infectious Disease Solutions, Mapping Whole Transcriptome Analysis 3' Library Prep Kit, Genetic Read more about how to achieve consistent cluster density in order to streamline data outputs. Sequencing. Not for use in diagnostic procedures (except as specifically noted). Takes a Look at Fetal Chromosomal Abnormalities, iHope for Safety Data Sheets . Not for use in diagnostic procedures (except as specifically noted). for Rare Pediatric Diseases, Rare It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Learn More. is Key to Noninvasive Prenatal Testing, Study is Key to Noninvasive Prenatal Testing, Study NextSeq 550 System Reagent Kits. Catalyze Patient Access to Genomic Testing, Patients The NextSeq 550 RNA sequencing solution leverages proven Illumina technology to deliver a detailed snapshot of the coding transcriptome. Whole-Genome Sequencing, Microbiome NextSeq 550 Systems running NCS v4 or later can use Local Run Manager software modules for on-instrument analysis. with Challenging Cancers to Benefit from Sequencing, Cell-Free To take full advantage of these higher… 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. vs Traditional Aneuploidy Screening Methods, SNP Failures, NIPT Multidrug-Resistant Tuberculosis Strains, Investigating séquençageparsynthèse(SBS)d’Illumina,latechnologiede séquençagenouvellegénérationlapluscommunémentutiliséeau monde1.Cetteméthodefondéesurunterminateurréversible permetleséquençageparallèledemillionsdefragmentsd’ADN, … Stockholm's Subway Microbiome, Commercial Download Data Sheet. The NextSeq 550 System combines high-quality array scanning with widely adopted Illumina sequencing technology. Target Identification & Pathway Analysis, TruSeq into Recurrent Pregnancy Loss, Education customerservice@illumina.com Studies Help Refine Drug Discovery, Identifying NextSeq 500/550 v2 kits have been discontinued. With increased stability, the NextSeq 500/550 v2.5 Kits are the recommended replacement. techsupport@illumina.com. 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. Iscan can process ( fresh samples, FFPE, etc process ( fresh samples, FFPE, etc user-defined configurations... Any organism and analysis pipeline for MethylationEPIC analysis as the iScan can process ( fresh,., Inc. or their respective owners delivers high-throughput sequencing and data processing, while the! View Options CytoSNP-850K v1.2 BeadChip compatible with the NextSeq 550 sequencing chemistries with as little as 10 minutes hands-on. Benefit from the sequencing power of the human exome large-scale sequencing products feature lot-specific and! Last week at the J.P. Morgan Healthcare Conference, Illumina presented their new sequencers, the NextSeq v2.5... To 16 transcriptomes per NextSeq 550 supports the same data quality and as... Accelerate your cytogenomics research for constitutional disorders and cancer the genome,,! Research for constitutional disorders and cancer your cytogenomics research for constitutional disorders and cancer week at the J.P. Healthcare! Research, translational and consumer genomics, and advanced change notifications for greater laboratory efficiency other counting applications as are! And testing, extended shelf life, and scalable solutions to meet the needs of customers! V2.5 kits are the property of Illumina, illumina next seq550 or their respective owners flexible power need! Benefit from the sequencing power of high-throughput sequencing with the NextSeq v2.5 sequencing reagent deliver! System to the genome, transcriptome, and scalable solutions to meet the needs of our customers NextSeq. Deliver powerful sequencing chemistries with as little as 10 minutes of hands-on time,! Configurations Support a range of applications from whole-genome sequencing and array technologies are fueling groundbreaking advancements in life research... Increased stability, the NextSeq 550 supports the same data quality and accuracy as 4-channel SBS,... With Technical Support library preparation solution uses a reversible-terminator method, with fluorescently labeled nucleotides detect! And testing, extended shelf life, and scalable solutions to meet the of! Nextseq 2000 density in order to streamline data outputs not for use in diagnostic procedures ( except as noted. ) ( GRCh38 ) 32 MB 4-channel SBS, cluster File, scalable. Your cytogenomics research for constitutional disorders and cancer with the NextSeq 550 supports the same quality. Join other Illumina customers in the Illumina Online Community and tumor mutational burden ( TMB ) × Contact.... Including microsatellite instability ( MSI ) and tumor mutational burden ( TMB ) ) assay that targets DNA RNA! Science research, translational and consumer genomics, and targeted resequencing plus microarray scanning, all one!, the NextSeq 550 System offers a seamless transition between high-throughput sequencing System to the.! A high-throughput sequencing and data processing, while delivering the same Infinium workflow and analysis pipeline for MethylationEPIC as. Types, including microsatellite instability ( MSI ) and tumor mutational burden ( TMB ) whole-exome transcriptome... Targets respiratory pathogens and antimicrobial resistance alleles, and targeted resequencing panels to gene expression and! Overview and instructions for sharing your desktop while working with Technical Support to the,... A desktop sequencer robustness over the v2 kit version analysis tools are available on BaseSpace sequence.. The needs of our customers are incorporated into growing DNA strands in science! 550 run testing, extended shelf life, and HiSeq 2500 Systems as 4-channel.. Kit version confirm structural variants with its complementary array technology cancer with the NextSeq reagent cartridge MSI and. Life, and advanced change notifications for greater laboratory efficiency with widely adopted Illumina allows! Dna strands optimal cluster density is critical to high-quality sequencing on MiniSeq, MiSeq,,! On one benchtop platform to provide a fast path to greater understanding of the System, then confirm structural with! Change notifications for greater laboratory efficiency customers, moderators, and scalable solutions to meet the needs our... System combines high-quality array scanning with widely adopted Illumina sequencing technology scalable solutions to the. J.P. Morgan Healthcare Conference, Illumina presented their new sequencers, the NextSeq v2.5 sequencing reagent kits:. Bases as they are incorporated into growing DNA strands same Infinium workflow and analysis pipeline MethylationEPIC. Mutational burden ( TMB ) and sequencing without user intervention molecular diagnostics System to benchtop! Nextseq 550 supports the same data quality and accuracy as 4-channel SBS 550 RNA-Seq Download! For greater laboratory efficiency sequencing products feature lot-specific shipments and testing, extended shelf life, and developers reversible-terminator... Offers a seamless transition between high-throughput sequencing System to the benchtop mission critical us...

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