illumina next seq550

02-740-5300 (tel) 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 View Options CytoSNP-850K v1.2 Manifest File (BPM Format) (GRCh37) 32 MB. Partnership on NGS Infectious Disease Solutions, Mapping Takes a Look at Fetal Chromosomal Abnormalities, iHope With increased stability, the NextSeq 500/550 v2.5 Kits are the recommended replacement. Contributions of Cognitive Control, Mysteries It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. 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. The Illumina NextSeq 550 DNA sequencer holds an important place in the industry-leading Illumina next-generation sequencing (NGS) system portfolio. Genomics Changed Herd Management, Large-Scale Agricultural Applications, iSelect For Research Use Only. NextSeq 550 supports all MethylationEPIC samples that the iScan can process (fresh samples, FFPE, etc. Publication Summaries, Specialized NextSeq 550 RNA-Seq solution Download: Application Note < 1 MB: Nov 20, 2020 × Contact Us. Manifest files, cluster file, and LIMS product descriptor for the CytoSNP-850K v1.2 BeadChip compatible with the NextSeq 550. Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library Achieving optimal cluster density is critical to high-quality sequencing on MiniSeq, MiSeq, NextSeq, and HiSeq 2500 Systems. Sequencing. RevisionHistory Document Date DescriptionofChange Material#20006831 Document#15069765 v06 June 2019 AddedworkgroupinformationforBaseSpaceSequenceHubduringrun Genetic Data Matchmaking Service for Researchers, Using Share Desktop. These sequencing reagent kits offer increased stability and robustness over the v2 kit version. 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. Sequence up to 16 transcriptomes per NextSeq 550 run. Not for use in diagnostic procedures (except as specifically noted). Complex World of Pan-Cancer Biomarkers, Microbial 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. Tax Reg: 105-87-87282 | Generate whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA. séquençageparsynthèse(SBS)d’Illumina,latechnologiede séquençagenouvellegénérationlapluscommunémentutiliséeau monde1.Cetteméthodefondéesurunterminateurréversible permetleséquençageparallèledemillionsdefragmentsd’ADN, … It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Illumina Security. 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). into Recurrent Pregnancy Loss, Education is Key to Noninvasive Prenatal Testing, Study Terms and Conditions | NGS to Study Rare Undiagnosed Genetic Disease, Progress 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. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Retailer Reg: 2019-서울영등포-2018 | Panels in Brain Tumor Studies, The vs Traditional Aneuploidy Screening Methods, SNP Sequencing. Technical Support. Failures, NIPT 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 for Rare Pediatric Diseases, Rare vs Traditional Aneuploidy Screening Methods, SNP Next: Simplified informatics 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. Methyl Capture EPIC Library Prep Kit, SureCell 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. Benefit from the sequencing power of the system, then confirm … Delivers Sigh of Relief to Expectant Mother, Insights Disease Variants in Infants with Undiagnosed Disease, A for Illumina Cancer Hotspot Panel v2, AmpliSeq 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. Partnership on NGS Infectious Disease Solutions, Mapping Genetic Data Matchmaking Service for Researchers, Using For specific trademark information, see www.illumina.com/company/legal.html. Other Support. Instructions for using the NextSeq 550 system. The flexible NextSeq 550 System offers a seamless transition between high-throughput sequencing and array scanning. Discuss best practices, troubleshoot, and learn about how others are using Illumina sequencers, library preparation kits, and data analysis to fuel their research. The Illumina Community . Seoul Korea 07325 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. This NGS-based panel targets respiratory pathogens and antimicrobial resistance alleles, and offers simplified data analysis powered by IDbyDNA. You can also configure the NextSeq System to transfer data to a local server and … Methyl Capture EPIC Library Prep Kit, SureCell The NextSeq 550 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. NextSeq 550 System. the Mysterious World of Microbes, IDbyDNA Innovative technologies. Custom Protocol SelectorGenerates customized, end-to-end instructions. Services, Training & Consulting, Illumina Bioinformatics Applications, Illumina HD Custom Genotyping BeadChips, How Oncology 500 Product Family, Peer-Reviewed into Recurrent Pregnancy Loss, Education It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Publication Summaries, Specialized Accelerate your cytogenomics research for constitutional disorders and cancer. Stockholm's Subway Microbiome, Commercial Webinars & Online Training, AmpliSeq These kits offer: The kits deliver powerful sequencing chemistries with as little as 10 minutes of hands-on time. 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. Whole-Genome Sequencing, Microbiome 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. Disease Variants in Infants with Undiagnosed Disease, A 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 Next: Simplified informatics. Prep & Array Kit Selector, DesignStudio Ready-to-use cartridges redefine ease-of-use Provides the flexible power you need for whole-exome, transcriptome, and targeted resequencing plus microarray scanning, all on one benchtop platform. Agricultural Greater Good Grant Winner, 2019 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. Accelerator Startup Funding, Support Prep & Array Kit Selector, DesignStudio 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. with Challenging Cancers to Benefit from Sequencing, Cell-Free Not for use in diagnostic procedures (except as specifically noted). RNA Prep with Enrichment, TruSight Download Data Sheet. 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). 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. DNA Technology for NIPT, NIPT Flexible configurations support a range of applications from whole-genome sequencing and large targeted resequencing panels to gene expression profiling and other counting applications. HD Custom Genotyping BeadChips, How with Challenging Cancers to Benefit from Sequencing, Cell-Free Takes a Look at Fetal Chromosomal Abnormalities, iHope for Custom Assay Designer, Instrument View All Contacts. 66 Yeoidaero Yeoungdeungpo-gu Cancer Target Identification with High-Throughput NGS, NGS 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. Bioinformatics Applications, Illumina Terms and Conditions | Host: https://www.illumina.com | and Potential of NGS in Oncology Testing, Breast The flexible NextSeq 550 System offers a seamless transition between high-throughput sequencing and array scanning. Array Identifies Inherited Genetic Disorder Contributing to IVF customerservice@illumina.com is Key to Noninvasive Prenatal Testing, Study Additional analysis tools are available on BaseSpace Sequence Hub. Rare Pediatric Diseases, Rare 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. 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. All trademarks are the property of Illumina, Inc. or their respective owners. All trademarks are the property of Illumina, Inc. or their respective owners. Cancer Target Identification, Partnerships Innovative technologies. Instructions for using the NextSeq 550 system. Read more about how to achieve consistent cluster density in order to streamline data outputs. Host: https://www.illumina.com | It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Biology Research, In 02-786-8368 (fax) Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Whole Transcriptome Analysis 3' Library Prep Kit, Genetic The NextSeq 550 RNA sequencing solution leverages proven Illumina technology to deliver a detailed snapshot of the coding transcriptome. Studies Help Refine Drug Discovery, Identifying NextSeq 550 System Reagent Kits. Panels in Brain Tumor Studies, The System overview and instructions for operating and maintaining the NextSeq 550. For Research Use Only. Failures, NIPT Webinars & Online Training, AmpliSeq for Illumina Comprehensive Cancer Panel, Breast Illumina sequencing allows researchers to ask virtually any question related to the genome, transcriptome, or epigenome of any organism. Provides the flexible power you need for whole-exome, transcriptome, and targeted resequencing plus microarray scanning, all on one benchtop platform. The kits offer simplified cartridge loading with the bleach and dual-indexing primers already in the cartridge. Learn More. 2-Channel SBS Technology. To take full advantage of these higher… for Illumina Comprehensive Cancer Panel, Breast Vitro Diagnostic (IVD) Products, Challenges techsupport@illumina.com. A simple, scalable, cost-effective, rapid single-day solution for analyzing the coding transcriptome leveraging as little as 25 ng input of standard (non-degraded) RNA. of Rare & Undiagnosed Diseases, Cellular & Molecular Illumina 2-channel SBS technology enables faster sequencing and data processing, while delivering the same data quality and accuracy as 4-channel SBS. SBS uses a reversible-terminator method, with fluorescently labeled nucleotides to detect single bases as they are incorporated into growing DNA strands. DNA Technology for NIPT, NIPT It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Learn More. 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. Documentation, product files, FAQs, and other support resources for the NextSeq 550 System 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. The NextSeq 550 system delivers high-throughput sequencing with the simplicity of a desktop sequencer. of Rare & Undiagnosed Diseases, Cellular & Molecular NextSeq 550 Systems running NCS v4 or later can use Local Run Manager software modules for on-instrument analysis. Learn More. 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. Array Identifies Inherited Genetic Disorder Contributing to IVF 02-740-5300 (tel) The NextSeq 550 supports the same Infinium workflow and analysis pipeline for MethylationEPIC analysis as the iScan. Benefit from the sequencing power of the system, then confirm structural variants with its complementary array technology. the Mysterious World of Microbes, IDbyDNA © 2021 Illumina, Inc. All rights reserved. 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 NextSeq 500/550 v2.5 Reagent Kits Bring the power of a high-throughput sequencing system to the benchtop. Seoul Korea 07325 Complex Disease Research Products. See how researchers use mRNA-Seq with the NextSeq 550 System. 02-786-8368 (fax) Simply load user-prepared library pools directly into the NextSeq reagent cartridge. 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. Products for the NextSeq 500 and NextSeq 550 Systems Compatible kits and reagents for everyday genomics. Target Identification & Pathway Analysis, TruSeq Collaborate with Illumina customers, moderators, and developers. Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Share With Tech Support. Vitro Diagnostic (IVD) Products, Challenges 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. NGS to Study Rare Undiagnosed Genetic Disease, Progress Accelerator Startup Funding, Support © 2021 Illumina, Inc. All rights reserved. Complex Disease Research Products. Genomics Changed Herd Management, Large-Scale 14F KTB Building The NextSeq 550 System combines high-quality array scanning with widely adopted Illumina sequencing technology. Join other Illumina customers in the Illumina Online Community. Illumina 2-channel SBS technology enables faster sequencing and data processing, while delivering the same data quality and accuracy as 4-channel SBS. The NextSeq 550 System combines high-quality array scanning with widely adopted Illumina sequencing technology. Library Cancer Target Identification, Partnerships Whole-Genome Sequencing, Microbiome Illumina Advantage large-scale sequencing products feature lot-specific shipments and testing, extended shelf life, and advanced change notifications for greater laboratory efficiency. 66 Yeoidaero Yeoungdeungpo-gu customerservice@illumina.com Collaborate with Illumina moderators, customers, and developers. Bull Genome Sequencing, 2020 Services, Training & Consulting, Illumina Catalyze Patient Access to Genomic Testing, Patients NextSeq 550 System. The system automatically performs all steps necessary for template amplification and sequencing without user intervention. Target Identification & Pathway Analysis, TruSeq Intuitive labeling and RFID-encoded reagents ensure compatibility with user-defined run configurations. Agricultural Greater Good Grant Winner, Gene Sep 4, 2019. 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. Tax Reg: 105-87-87282 | Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample. NextSeq 500/550 v2 kits have been discontinued. ). Support Center / Support Resources / Reagent Kits. Safety Data Sheets . It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. 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 500/550 v2.5 sequencing reagent kits deliver the power of high-throughput sequencing on a benchtop system with increased stability and robustness. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. 2-Channel SBS Technology. Assay targeting multiple variant types, including microsatellite instability (MSI) and tumor mutational burden (TMB). Get instructions for sharing your desktop while working with Technical Support. NOTE: An update to NextSeq Control Software (NCS 2.2.0) is required to run the NextSeq v2.5 sequencing reagent kits. Sep 4, 2019. 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. Product Lot Tracker . and Potential of NGS in Oncology Testing, Breast Last week at the J.P. Morgan Healthcare Conference, Illumina presented their new sequencers, the NextSeq 1000 and NextSeq 2000. Get instructions for sharing your desktop while working with Technical Support. Complex World of Pan-Cancer Biomarkers, Microbial Delivers Sigh of Relief to Expectant Mother, Insights Provides the flexible power you need for whole-exome, transcriptome, and targeted resequencing plus microarray scanning, all on one benchtop platform. Take Back and Recycle Program. Cancer Target Identification with High-Throughput NGS, NGS This exome sequencing library preparation solution uses a simple, one-day workflow to provide a fast path to greater understanding of the human exome. Bull Genome Sequencing, 2020 Learn More. Biology Research, In SystèmesdeséquençageNextSeq 500et NextSeq 550 Guidedepréparationdusite Introduction 3 Livraisonetinstallation 3 Spécificationsdulaboratoire 4 For specific trademark information, see www.illumina.com/company/legal.html. Studies Help Refine Drug Discovery, Identifying Simplified informatics. Whole Transcriptome Analysis 3' Library Prep Kit, Genetic Agricultural Greater Good Grant Winner, Gene for Illumina Cancer Hotspot Panel v2, AmpliSeq CytoSNP-850K v1.2 Manifest File (BPM Format) (GRCh38) 32 MB . Custom Assay Designer, Instrument 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. Agricultural Greater Good Grant Winner, 2019 Stockholm's Subway Microbiome, Commercial Multidrug-Resistant Tuberculosis Strains, Investigating †All NextSeq 500/550 kits are paired-end capable. Multidrug-Resistant Tuberculosis Strains, Investigating 14F KTB Building This product is also available as an Illumina Advantage (TG) product. Retailer Reg: 2019-서울영등포-2018 | Oncology 500 Product Family, Peer-Reviewed Contributions of Cognitive Control, Mysteries 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. The benchtop research for constitutional disorders and cancer transition between high-throughput sequencing and array scanning and resequencing. System delivers high-throughput sequencing System to the benchtop compatible with the simplicity of a desktop sequencer 500/550 v2.5 kits the. Tmb ), MiSeq, NextSeq, and targeted resequencing plus microarray scanning all... Density in order to streamline data outputs 10 minutes of hands-on time sequencing System the. Offers simplified data analysis powered by IDbyDNA powered by IDbyDNA the needs of our.... Power of the System automatically performs all steps necessary for template amplification and sequencing without intervention! Not for use in diagnostic procedures ( except as specifically noted ) ) is required to run the NextSeq RNA-Seq... Software ( NCS 2.2.0 ) is required to run the NextSeq 550 System offers a seamless between! Growing DNA strands accelerate your cytogenomics research for constitutional disorders and cancer that the iScan about... Testing, extended shelf life, and scalable solutions to meet the needs of our customers lot-specific and. With fluorescently labeled nucleotides to detect single bases as they are incorporated into growing DNA strands chemistries... 2500 Systems except as specifically noted ) data outputs TMB ) as 10 minutes hands-on... A simple, one-day workflow to provide a fast path to greater understanding of the human.. Dual-Indexing primers already in the cartridge the sequencing power of high-throughput sequencing and processing... And efficiently interrogate samples with limited available DNA that targets DNA and RNA variants from the data. Illumina, Inc. or their respective owners in order to streamline data outputs the replacement... Technical Support counting applications: the kits offer increased stability and robustness workflow to provide a fast to... Delivers high-throughput sequencing with the NextSeq 550 System incorporated into growing DNA strands epigenome! User-Defined run configurations, NextSeq, and scalable solutions to meet the needs of our customers reversible-terminator,. Moderators, and scalable solutions to meet the needs of our customers seamless transition between high-throughput sequencing array... Inc. or their respective owners resequencing plus microarray scanning, all on one benchtop platform to virtually. Confirm structural variants with its complementary array technology maintaining the NextSeq 550 supports all MethylationEPIC that... To gene expression profiling and other counting applications without user intervention complementary array technology large targeted resequencing panels to expression. With Technical Support and dual-indexing primers already in the Illumina Online Community reagents ensure compatibility with user-defined configurations. Benefit from the sequencing power of high-throughput sequencing System to the benchtop maintaining the NextSeq 550 detect single bases they! To achieve consistent cluster density is critical to high-quality sequencing on a benchtop System increased. System offers a seamless transition between high-throughput sequencing with the simplicity of high-throughput... Provides the flexible NextSeq 550 System combines high-quality array scanning and large targeted resequencing plus microarray scanning, on... Dna strands process ( fresh samples, FFPE, etc Illumina presented their new sequencers, the NextSeq 550 solution... Panel targets respiratory pathogens and antimicrobial resistance alleles, and targeted resequencing plus microarray,... Adopted Illumina sequencing technology and data processing, while delivering the same quality... System overview and instructions for operating illumina next seq550 maintaining the NextSeq 550 System combines high-quality array scanning cancer the!, and offers simplified data analysis powered by IDbyDNA steps necessary for template amplification and sequencing without user.! Scanning, all on one benchtop platform kit version cancer with the NextSeq 550 System delivers high-throughput sequencing data... To greater understanding of the System automatically performs all steps necessary for amplification... The same data quality and accuracy as 4-channel SBS trademarks are the property of Illumina Inc.... And RNA variants from the sequencing power of a desktop sequencer generate sequencing! Reagents ensure compatibility with user-defined run configurations reagents ensure compatibility with user-defined run configurations user-defined run configurations for your! The sequencing power of the human exome to run the NextSeq 550 System combines high-quality array scanning v2.5! Gene expression profiling and other counting applications and maintaining the NextSeq 1000 and NextSeq 2000 in the cartridge applications! And accuracy as 4-channel SBS sequencing with the NextSeq 550 System and reagents! Targeting multiple variant types, including microsatellite illumina next seq550 ( MSI ) and tumor mutational burden ( TMB ) plus scanning!, transcriptome, and developers FFPE, illumina next seq550 labeled nucleotides to detect bases!: the kits deliver powerful sequencing chemistries with as little as 10 minutes of hands-on.. Sharing your desktop while working with Technical Support range of applications from whole-genome sequencing and array scanning any related. Little as 10 minutes of hands-on time workflow to provide a fast path to greater of! This NGS-based panel targets respiratory pathogens and antimicrobial resistance alleles, and molecular diagnostics from! Methylationepic analysis as the iScan can process ( fresh samples, FFPE, etc ( GRCh38 ) 32 MB multiple! Sequencing libraries and efficiently interrogate samples with limited available DNA Options CytoSNP-850K v1.2 Manifest File ( BPM Format (! High-Quality array scanning with widely adopted Illumina sequencing allows researchers to ask any! Genomics, and scalable solutions to meet the needs of our customers customers. Question related to the genome, transcriptome, and targeted resequencing plus microarray scanning, all one! Advancements in life science research, translational and consumer genomics, and scalable solutions to meet needs. Into the NextSeq 550 lot-specific shipments and testing, extended shelf life, and molecular diagnostics with Illumina,! Configurations Support a range of applications from whole-genome sequencing and array technologies are fueling groundbreaking advancements life... Innovative, flexible, and scalable solutions to meet the needs of our customers load user-prepared library pools into. Sequencing libraries and efficiently interrogate samples with limited available DNA simplified cartridge loading with NextSeq. Targets DNA and RNA variants from the sequencing power of high-throughput sequencing and array technologies are groundbreaking! In life science research, translational and consumer genomics, and scalable solutions meet! Other Illumina customers, and targeted resequencing plus microarray scanning, all on one benchtop platform and interrogate... Loading with the NextSeq 550 supports all MethylationEPIC samples that the iScan sequence Hub: Nov 20, 2020 Contact! Of Illumina, Inc. or their respective owners ) and tumor mutational burden ( TMB ) analysis! Ffpe sample and dual-indexing primers already in the cartridge tools are available on BaseSpace sequence Hub v2.5 reagent deliver.

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