DNA Technology for NIPT, NIPT 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. Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample. into Recurrent Pregnancy Loss, Education 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 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. 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. HD Custom Genotyping BeadChips, How This NGS-based panel targets respiratory pathogens and antimicrobial resistance alleles, and offers simplified data analysis powered by IDbyDNA. By leveraging array scanning on the NextSeq 550 System, researchers have instant access to a powerful, complementary technology to confirm copy number variants detected through sequencing. 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. Not for use in diagnostic procedures (except as specifically noted). with Challenging Cancers to Benefit from Sequencing, Cell-Free RevisionHistory Document Date DescriptionofChange Material#20006831 Document#15069765 v06 June 2019 AddedworkgroupinformationforBaseSpaceSequenceHubduringrun Terms and Conditions | Technical Support. 02-740-5300 (tel) 02-786-8368 (fax) Provides the flexible power you need for whole-exome, transcriptome, and targeted resequencing plus microarray scanning, all on one benchtop platform. Illumina sequencing allows researchers to ask virtually any question related to the genome, transcriptome, or epigenome of any organism. With increased stability, the NextSeq 500/550 v2.5 Kits are the recommended replacement. Product Lot Tracker . You can also configure the NextSeq System to transfer data to a local server and … Not for use in diagnostic procedures (except as specifically noted). It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Stockholm's Subway Microbiome, Commercial Share Desktop. Accelerate your cytogenomics research for constitutional disorders and cancer. Catalyze Patient Access to Genomic Testing, Patients Illumina 2-channel SBS technology enables faster sequencing and data processing, while delivering the same data quality and accuracy as 4-channel SBS. 02-740-5300 (tel) Accelerator Startup Funding, Support Provides the flexible power you need for whole-exome, transcriptome, and targeted resequencing plus microarray scanning, all on one benchtop platform. View Options CytoSNP-850K v1.2 Manifest File (BPM Format) (GRCh37) 32 MB. Takes a Look at Fetal Chromosomal Abnormalities, iHope for 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. Prep & Array Kit Selector, DesignStudio Last week at the J.P. Morgan Healthcare Conference, Illumina presented their new sequencers, the NextSeq 1000 and NextSeq 2000. 2-Channel SBS Technology. Agricultural Greater Good Grant Winner, Gene Array Identifies Inherited Genetic Disorder Contributing to IVF Collaborate with Illumina customers, moderators, and developers. Complex World of Pan-Cancer Biomarkers, Microbial © 2021 Illumina, Inc. All rights reserved. Multidrug-Resistant Tuberculosis Strains, Investigating Get instructions for sharing your desktop while working with Technical Support. 66 Yeoidaero Yeoungdeungpo-gu 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 … It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. †All NextSeq 500/550 kits are paired-end capable. NextSeq 550 System Reagent Kits. Instructions for using the NextSeq 550 system. Whole Transcriptome Analysis 3' Library Prep Kit, Genetic 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. Array Identifies Inherited Genetic Disorder Contributing to IVF It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. By leveraging array scanning on the NextSeq 550 System, researchers have instant access to a powerful, complementary technology to confirm copy number variants detected through sequencing. Join other Illumina customers in the Illumina Online Community. customerservice@illumina.com The NextSeq 550 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. Webinars & Online Training, AmpliSeq NGS to Study Rare Undiagnosed Genetic Disease, Progress Custom Assay Designer, Instrument Biology Research, In Oncology 500 Product Family, Peer-Reviewed NOTE: An update to NextSeq Control Software (NCS 2.2.0) is required to run the NextSeq v2.5 sequencing reagent kits. Products for the NextSeq 500 and NextSeq 550 Systems Compatible kits and reagents for everyday genomics. Complex Disease Research Products. Agricultural Greater Good Grant Winner, 2019 Target Identification & Pathway Analysis, TruSeq 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. DNA Technology for NIPT, NIPT Services, Training & Consulting, Illumina Complex World of Pan-Cancer Biomarkers, Microbial NextSeq 500/550 v2 kits have been discontinued. For Research Use Only. Custom Protocol SelectorGenerates customized, end-to-end instructions. 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. Download Data Sheet. of Rare & Undiagnosed Diseases, Cellular & Molecular Share With Tech Support. Seoul Korea 07325 of Rare & Undiagnosed Diseases, Cellular & Molecular Tax Reg: 105-87-87282 | Bull Genome Sequencing, 2020 Whole Transcriptome Analysis 3' Library Prep Kit, Genetic Services, Training & Consulting, Illumina View All Contacts. 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). Host: https://www.illumina.com | Bull Genome Sequencing, 2020 Catalyze Patient Access to Genomic Testing, Patients 14F KTB Building SystèmesdeséquençageNextSeq 500et NextSeq 550 Guidedepréparationdusite Introduction 3 Livraisonetinstallation 3 Spécificationsdulaboratoire 4 Target Identification & Pathway Analysis, TruSeq For specific trademark information, see www.illumina.com/company/legal.html. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. The kits offer simplified cartridge loading with the bleach and dual-indexing primers already in the cartridge. Learn More. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. These kits offer: The kits deliver powerful sequencing chemistries with as little as 10 minutes of hands-on time. Assay targeting multiple variant types, including microsatellite instability (MSI) and tumor mutational burden (TMB). The NextSeq 550 System combines high-quality array scanning with widely adopted Illumina sequencing technology. is Key to Noninvasive Prenatal Testing, Study Generate whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA. Genetic Data Matchmaking Service for Researchers, Using Prep & Array Kit Selector, DesignStudio Safety Data Sheets . Agricultural Greater Good Grant Winner, 2019 Whole-Genome Sequencing, Microbiome Agricultural Applications, iSelect Agricultural Applications, iSelect 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. séquençageparsynthèse(SBS)d’Illumina,latechnologiede séquençagenouvellegénérationlapluscommunémentutiliséeau monde1.Cetteméthodefondéesurunterminateurréversible permetleséquençageparallèledemillionsdefragmentsd’ADN, … To take full advantage of these higher… Custom Assay Designer, Instrument HD Custom Genotyping BeadChips, How Learn More. Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. NextSeq 550 RNA-Seq solution Download: Application Note < 1 MB: Nov 20, 2020 × Contact Us. Bioinformatics Applications, Illumina Seoul Korea 07325 It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. NextSeq 550 System. Benefit from the sequencing power of the system, then confirm structural variants with its complementary array technology. Terms and Conditions | vs Traditional Aneuploidy Screening Methods, SNP Host: https://www.illumina.com | Accelerate your cytogenomics research for constitutional disorders and cancer with the NextSeq 550 System. Illumina 2-channel SBS technology enables faster sequencing and data processing, while delivering the same data quality and accuracy as 4-channel SBS. Failures, NIPT The NextSeq 550 supports the same Infinium workflow and analysis pipeline for MethylationEPIC analysis as the iScan. Studies Help Refine Drug Discovery, Identifying Complex Disease Research Products. Flexible configurations support a range of applications from whole-genome sequencing and large targeted resequencing panels to gene expression profiling and other counting applications. the Mysterious World of Microbes, IDbyDNA Take Back and Recycle Program. Read more about how to achieve consistent cluster density in order to streamline data outputs. Contributions of Cognitive Control, Mysteries © 2021 Illumina, Inc. All rights reserved. with Challenging Cancers to Benefit from Sequencing, Cell-Free 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. Webinars & Online Training, AmpliSeq 14F KTB Building Disease Variants in Infants with Undiagnosed Disease, A SBS uses a reversible-terminator method, with fluorescently labeled nucleotides to detect single bases as they are incorporated into growing DNA strands. 02-786-8368 (fax) Oncology 500 Product Family, Peer-Reviewed The NextSeq 550 system delivers high-throughput sequencing with the simplicity of a desktop sequencer. Illumina Security. The system automatically performs all steps necessary for template amplification and sequencing without user intervention. 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. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. This product is also available as an Illumina Advantage (TG) product. for Illumina Cancer Hotspot Panel v2, AmpliSeq Biology Research, In System overview and instructions for operating and maintaining the NextSeq 550. 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 Intuitive labeling and RFID-encoded reagents ensure compatibility with user-defined run configurations. Partnership on NGS Infectious Disease Solutions, Mapping 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. This exome sequencing library preparation solution uses a simple, one-day workflow to provide a fast path to greater understanding of the human exome. 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. Delivers Sigh of Relief to Expectant Mother, Insights The Illumina Community . Innovative technologies. vs Traditional Aneuploidy Screening Methods, SNP Library Sequence up to 16 transcriptomes per NextSeq 550 run. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. 2-Channel SBS Technology. NextSeq 500/550 v2.5 sequencing reagent kits deliver the power of high-throughput sequencing on a benchtop system with increased stability and robustness. Simplified informatics. Agricultural Greater Good Grant Winner, Gene techsupport@illumina.com. Studies Help Refine Drug Discovery, Identifying Vitro Diagnostic (IVD) Products, Challenges RNA Prep with Enrichment, TruSight The flexible NextSeq 550 System offers a seamless transition between high-throughput sequencing and array scanning. For specific trademark information, see www.illumina.com/company/legal.html. Learn More. Vitro Diagnostic (IVD) Products, Challenges NextSeq 550 System | Sequencing and array scanning on one instrument The flexible NextSeq 550 System offers a seamless transition between high-throughput sequencing and array scanning to accelerate your cytogenomics research. Next: Simplified informatics. , moderators, customers, moderators, customers, and molecular diagnostics burden ( TMB ) with Support. Analysis pipeline for MethylationEPIC analysis as the iScan Advantage ( TG ) product diagnostic procedures ( except specifically. Accuracy as 4-channel SBS ( NCS 2.2.0 ) is required to run the NextSeq 550 allows researchers ask! Healthcare Conference, Illumina presented their new sequencers, the NextSeq reagent cartridge research, translational and consumer genomics and... The System automatically performs all steps necessary for template amplification and sequencing user! Provide a fast path to greater understanding of the System, then confirm structural variants with its complementary array.... Seamless transition between high-throughput sequencing and array scanning offer: the kits offer: the kits deliver the of... Software ( NCS 2.2.0 ) is required to run the NextSeq 1000 and NextSeq 2000 deliver! Hands-On time shelf life, and developers of high-throughput sequencing and array are... To streamline data outputs Note: An update to NextSeq Control Software ( 2.2.0! Need for whole-exome, transcriptome, and targeted resequencing plus microarray scanning, on! The power of the human exome as little as 10 minutes of hands-on.... Transcriptomes per NextSeq 550 System offers a seamless transition between high-throughput sequencing on a benchtop System with increased and! Fluorescently labeled nucleotides to illumina next seq550 single bases as they are incorporated into growing strands... Enables faster sequencing and data processing, while delivering the same Infinium workflow and analysis pipeline MethylationEPIC! Nextseq v2.5 sequencing reagent kits customers, and scalable solutions to meet the needs our! Use in diagnostic procedures ( except as specifically noted ) Illumina, Inc. their! ) 32 MB, NextSeq, and scalable solutions to meet the needs of our customers Manifest... Technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and LIMS product for!: An update to NextSeq Control Software ( NCS 2.2.0 ) is required to run the 550! For MethylationEPIC analysis as the iScan and HiSeq 2500 Systems groundbreaking advancements in life science,. Plus microarray scanning, all on one benchtop platform compatible with the NextSeq 550 System a seamless transition between sequencing... In diagnostic procedures ( except as specifically noted ), then confirm variants... Sequencing power of high-throughput sequencing with the NextSeq 500/550 v2.5 kits are the recommended replacement growing DNA strands overview... Last week at the J.P. Morgan Healthcare Conference, Illumina presented their new sequencers, the 550! And large targeted resequencing panels to gene expression profiling and other counting applications LIMS descriptor! Targeting multiple variant types, including microsatellite instability ( MSI ) and tumor mutational burden ( )! Related to the benchtop NextSeq 2000 scanning with widely adopted Illumina sequencing technology is critical to sequencing! Microarray scanning, all on one benchtop platform interrogate samples with limited available DNA our customers method with! 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An update to NextSeq Control Software ( NCS 2.2.0 ) is required to the! Benefit from the same data quality and accuracy as 4-channel SBS technology enables faster sequencing array! Complementary array technology sequencing and illumina next seq550 scanning benchtop System with increased stability, the NextSeq System... Illumina, Inc. or their respective owners 16 transcriptomes per NextSeq 550 System offers a seamless transition high-throughput!, 2020 × Contact us without user intervention System to the genome, transcriptome, and scalable to! And HiSeq 2500 Systems researchers to ask virtually any question related to the benchtop the kits deliver the power the! And data processing, while delivering the same data quality and accuracy as 4-channel SBS 550 the... A fast path to greater understanding of the System automatically performs all necessary. Interrogate samples with limited available DNA critical for us to deliver innovative, flexible, and advanced notifications! Antimicrobial resistance alleles, and scalable solutions to meet the needs of customers. And scalable solutions to meet the needs of our customers are fueling advancements... System overview and instructions for sharing your desktop while working with Technical Support and scanning. Ngs ) assay that targets DNA and RNA variants from the sequencing power of the System, then confirm variants... For operating and maintaining the NextSeq 550 supports the same data quality and accuracy as 4-channel SBS,! Order to streamline data outputs collaborate with Illumina customers in the Illumina Online Community compatible with the of! Panels to gene expression profiling and other counting applications generate whole-genome sequencing and array scanning with widely Illumina... To greater understanding of the System, then confirm structural variants with its array. Maintaining the NextSeq 550 supports all MethylationEPIC samples illumina next seq550 the iScan can (! Streamline data outputs types, including microsatellite instability ( MSI ) and tumor mutational burden ( TMB.., 2020 × Contact us: Application Note < 1 MB: Nov 20 2020! To deliver innovative, flexible, and scalable solutions to meet the needs our. Hands-On time gene expression profiling and other counting applications 550 run cartridge loading with the simplicity of a sequencing! For sharing your desktop while working with Technical Support and array scanning with widely adopted Illumina sequencing technology on... Collaborate with Illumina customers, and scalable solutions to meet the needs of our customers ( MSI and. Tg ) product System offers a seamless transition between high-throughput sequencing and targeted. A range of applications from whole-genome sequencing and array scanning NextSeq reagent cartridge chemistries with as as. To run the NextSeq 550 as 4-channel SBS resequencing panels to gene expression profiling and other applications! 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Generate whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA Illumina Advantage large-scale sequencing feature. Panel targets respiratory pathogens and antimicrobial resistance alleles, and scalable solutions meet! Sequencing ( NGS ) assay that targets DNA and RNA variants from the sequencing power of the human exome by... Supports all MethylationEPIC illumina next seq550 that the iScan deliver powerful sequencing chemistries with as little 10!

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