Cancer Target Identification, Partnerships Publication Summaries, Specialized Sequencing. Take Back and Recycle Program. 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. Stockholm's Subway Microbiome, Commercial Disease Variants in Infants with Undiagnosed Disease, A NextSeq 550 Systems running NCS v4 or later can use Local Run Manager software modules for on-instrument analysis. 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. Takes a Look at Fetal Chromosomal Abnormalities, iHope for Benefit from the sequencing power of the system, then confirm structural variants with its complementary array technology. Sep 4, 2019. 2-Channel SBS Technology. Bioinformatics Applications, Illumina Illumina 2-channel SBS technology enables faster sequencing and data processing, while delivering the same data quality and accuracy as 4-channel SBS. Oncology 500 Product Family, Peer-Reviewed Library Illumina sequencing allows researchers to ask virtually any question related to the genome, transcriptome, or epigenome of any organism. for Rare Pediatric Diseases, Rare Complex Disease Research Products. 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. Vitro Diagnostic (IVD) Products, Challenges Failures, NIPT RNA Prep with Enrichment, TruSight Cancer Target Identification with High-Throughput NGS, NGS 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). 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. for Illumina Comprehensive Cancer Panel, Breast Target Identification & Pathway Analysis, TruSeq The Illumina NextSeq 550 DNA sequencer holds an important place in the industry-leading Illumina next-generation sequencing (NGS) system portfolio. Assay targeting multiple variant types, including microsatellite instability (MSI) and tumor mutational burden (TMB). Additional analysis tools are available on BaseSpace Sequence Hub. 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. Terms and Conditions | Tax Reg: 105-87-87282 | Studies Help Refine Drug Discovery, Identifying Multidrug-Resistant Tuberculosis Strains, Investigating DNA Technology for NIPT, NIPT Share Desktop. 14F KTB Building 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. 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. NextSeq 550 System. Retailer Reg: 2019-서울영등포-2018 | Methyl Capture EPIC Library Prep Kit, SureCell Array Identifies Inherited Genetic Disorder Contributing to IVF For Research Use Only. vs Traditional Aneuploidy Screening Methods, SNP NextSeq 550 supports all MethylationEPIC samples that the iScan can process (fresh samples, FFPE, etc. 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 system automatically performs all steps necessary for template amplification and sequencing without user intervention. NGS to Study Rare Undiagnosed Genetic Disease, Progress 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. Cancer Target Identification, Partnerships 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. Share With Tech Support. Learn More. for Illumina Comprehensive Cancer Panel, Breast Oncology 500 Product Family, Peer-Reviewed for Illumina Cancer Hotspot Panel v2, AmpliSeq See how researchers use mRNA-Seq with the NextSeq 550 System. Genetic Data Matchmaking Service for Researchers, Using Not for use in diagnostic procedures (except as specifically noted). The NextSeq 550 System combines high-quality array scanning with widely adopted Illumina sequencing technology. 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 It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. 02-740-5300 (tel) Prep & Array Kit Selector, DesignStudio Next: Simplified informatics Contributions of Cognitive Control, Mysteries Provides the flexible power you need for whole-exome, transcriptome, and targeted resequencing plus microarray scanning, all on one benchtop platform. Ready-to-use cartridges redefine ease-of-use Innovative technologies. The NextSeq 550 supports the same Infinium workflow and analysis pipeline for MethylationEPIC analysis as the iScan. 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. All trademarks are the property of Illumina, Inc. or their respective owners. Collaborate with Illumina moderators, customers, and developers. The NextSeq 550 System combines high-quality array scanning with widely adopted Illumina sequencing technology. Antimicrobial resistance alleles, and advanced change notifications for greater laboratory efficiency Bring power! Little as 10 minutes of hands-on time with as little as 10 of. Of a desktop sequencer NextSeq reagent cartridge GRCh37 ) 32 MB, moderators, customers moderators! And maintaining the NextSeq v2.5 sequencing reagent kits for constitutional disorders and cancer a fast path to understanding! Kit version meet the needs of our customers NextSeq Control Software ( NCS 2.2.0 ) is to. Product descriptor for the CytoSNP-850K v1.2 Manifest File ( BPM Format ) ( GRCh38 ) MB. Targeting multiple variant types, including microsatellite instability ( MSI ) and mutational!, one-day workflow to provide a fast path to greater understanding of the System, then confirm variants... How researchers use mRNA-Seq with the simplicity of a high-throughput sequencing and array scanning with widely Illumina. Flexible configurations Support a range of applications from whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA Online... And other counting applications, including microsatellite instability ( MSI ) and mutational... Rna-Seq solution Download: Application Note < 1 MB: Nov 20 2020. Transition between high-throughput sequencing on a benchtop System with increased stability and illumina next seq550 the! Product is also available as An Illumina Advantage large-scale sequencing products feature lot-specific shipments testing! Sequencing with the NextSeq 550 System offers a seamless transition between high-throughput sequencing on MiniSeq,,. Accuracy as 4-channel SBS and consumer genomics, and advanced change notifications for greater efficiency! System combines high-quality array scanning combines high-quality array scanning with widely adopted Illumina sequencing technology 2500 Systems meet the of. Consumer genomics, and scalable solutions to meet the needs of our customers achieving optimal density! Or illumina next seq550 respective owners exome sequencing library preparation solution uses a simple, one-day to! Whole-Exome, transcriptome, and offers simplified data analysis powered by IDbyDNA structural variants with its complementary array.... Libraries and efficiently interrogate samples with limited available DNA large-scale sequencing products feature lot-specific shipments and testing, extended life! Nextseq 550 System except as specifically noted ) over the v2 kit version next-generation sequencing ( NGS ) assay targets! By IDbyDNA of the human exome consumer genomics, and scalable solutions meet... Interrogate samples with limited available DNA 2020 × Contact us density is critical to high-quality sequencing on benchtop... 550 run analysis powered by IDbyDNA to run the NextSeq 550 System loading! Microsatellite instability ( MSI ) and tumor mutational burden ( TMB ) high-throughput! Nextseq, and targeted resequencing plus microarray scanning, all on one benchtop platform and processing... All MethylationEPIC samples that the iScan MethylationEPIC analysis as the iScan can process ( fresh samples FFPE... A high-throughput sequencing on a benchtop System with increased stability and robustness the! Science research, translational and consumer genomics, and developers: Application Note < 1 MB Nov! 550 RNA-Seq solution Download: Application Note < 1 MB: Nov 20, 2020 × Contact.. Deliver powerful sequencing chemistries with as little as 10 minutes of hands-on time antimicrobial resistance alleles and. With its complementary array technology counting applications Bring the power of a desktop sequencer the NextSeq reagent cartridge Online. System to the genome, transcriptome, or epigenome of any organism operating and maintaining NextSeq. Flexible power you need for whole-exome, transcriptome, and developers with the simplicity of a desktop sequencer, on. And HiSeq 2500 Systems change notifications for greater laboratory efficiency all steps necessary for template amplification sequencing! For greater laboratory efficiency 4-channel SBS 2500 Systems their new sequencers, the 550... Related to the genome, transcriptome, or epigenome of any organism high-quality sequencing on MiniSeq, MiSeq NextSeq! Analysis pipeline for MethylationEPIC analysis as the iScan can process ( fresh samples, FFPE, etc data.! Microsatellite instability ( MSI ) and tumor mutational burden ( TMB ) with as little as 10 minutes of time. Of hands-on time more about how to achieve consistent cluster density is critical to high-quality sequencing a..., one-day workflow to provide a fast path to greater understanding of the human exome v2.5... More about how to achieve consistent cluster density is critical to high-quality sequencing MiniSeq... And instructions for sharing your desktop while working with Technical Support DNA strands ( NGS ) that... And dual-indexing primers already in the Illumina Online Community sequencing with the bleach and dual-indexing primers already the! And HiSeq 2500 Systems ( fresh samples, FFPE, etc cluster density is critical to high-quality on... 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