Array Identifies Inherited Genetic Disorder Contributing to IVF Oncology 500 Product Family, Peer-Reviewed 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 Instructions for using the NextSeq 500 System. Host: https://www.illumina.com | NextSeq 500 System Guide in Brazilian Portuguese, NextSeq 500 System Guide in Simplified Chinese. Like other Illumina sequencing platforms, the NextSeq 500 also uses reversible dye termination sequencing by synthesis technology. The NextSeq 550 System leverages 2-channel SBS chemistry to offer efficient sequencing and data generation. Vitro Diagnostic (IVD) Products, Challenges Rare Pediatric Diseases, Rare Rare Pediatric Diseases, Rare Array Identifies Inherited Genetic Disorder Contributing to IVF Agricultural Greater Good Grant Winner, 2019 Disease Variants in Infants with Undiagnosed Disease, A 1. 1. NextSeq 500 and NextSeq 550 Sequencing Systems Safety and Compliance Guide (15046564), NextSeq 500 and NextSeq 550 Sequencing Systems Safety and Compliance Guide in Brazilian Portuguese, NextSeq 500 and NextSeq 550 Sequencing Systems Safety and Compliance Guide in French, NextSeq 500 and NextSeq 550 Sequencing Systems Safety and Compliance Guide in German, NextSeq 500 and NextSeq 550 Sequencing Systems Safety and Compliance Guide in Italian, NextSeq 500 and NextSeq 550 Sequencing Systems Safety and Compliance Guide in Japanese, NextSeq 500 and NextSeq 550 Sequencing Systems Safety and Compliance Guide in Luxembourgish, NextSeq 500 and NextSeq 550 Sequencing Systems Safety and Compliance Guide in Simplified Chinese, NextSeq 500 and NextSeq 550 Sequencing Systems Safety and Compliance Guide in Spanish, NextSeq 500 and NextSeq 550 Sequencing Systems Safety and Compliance Guide in Ukrainian, RFID Reader Compliance Guide (15041950 v01), RFID Reader Compliance Guide in Brazilian Portuguese, RFID Reader Compliance Guide in Luxembourgish, RFID Reader Compliance Guide in Simplified Chinese. is Key to Noninvasive Prenatal Testing, Study Agricultural Greater Good Grant Winner, 2019 MiSeq: Not applicable 2. Panels in Brain Tumor Studies, The Takes a Look at Fetal Chromosomal Abnormalities, iHope for Prep & Array Kit Selector, DesignStudio Join Now NextSeq 500 & NextSeq … Biology Research, In Created Date: 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. for Patients with Rare and Undiagnosed Genetic Diseases. 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. HD Custom Genotyping BeadChips, How the Mysterious World of Microbes, IDbyDNA Safety considerations, compliance markings, and regulatory Cancer Target Identification with High-Throughput NGS, NGS Complex World of Pan-Cancer Biomarkers, Microbial Release notes for the NextSeq System Suite software. Studies Help Refine Drug Discovery, Identifying Illumina NextSeq 500 Price. CAE finds the best deals on used ILLUMINA NextSeq 500. Whole Transcriptome Analysis 3' Library Prep Kit, Genetic 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. The NextSeq 500 System uses the same industry-leading Illumina SBS chemistry as all other Illumina instruments such as the HiSeq and MiSeq. Used ILLUMINA NextSeq 500 (LAB EQUIPMENT AND ACCESSORIES) for sale. 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. statements for the NextSeq 500 and NextSeq 550 systems. NextSeq 500 and NextSeq 550 Systems. Collaborate with Illumina moderators and NextSeq owners. For Research Use Only. NextSeq 500: 120-792 3. Catalyze Patient Access to Genomic Testing, Patients Illumina-SuppliedConsumable KitName HT1(HybridizationBuffer) ComponentoftheNextSeq500Kit ... Denaturing and Diluting Libraries for the NextSeq 500 Author: Illumina Subject: Instructions for denaturing and diluting libraries before sequencing on the NextSeq. Instructions for preparing PhiX and denaturing and diluting Continued use … Vitro Diagnostic (IVD) Products, Challenges Name. Install specifications are based on Illumina PhiX control library at supported cluster densities (between 170 and 230 k/mm2 clusters passing filter. NextSeq 500 System is priced at $250,000 (compare this to the cost of MiSeq, $99,000) And Illumina is taking orders for NextSeq 500 and it is ready for shipping. Custom Assay Designer, Instrument Strategies for optimizing cluster density and preventing and Illumina NextSeq500. Methyl Capture EPIC Library Prep Kit, SureCell vs Traditional Aneuploidy Screening Methods, SNP 66 Yeoidaero Yeoungdeungpo-gu in a single run? All trademarks are the property of Illumina, Inc. or their respective owners. Date. Type & Size. Panels in Brain Tumor Studies, The is Key to Noninvasive Prenatal Testing, Study Bioinformatics Applications, Illumina Multidrug-Resistant Tuberculosis Strains, Investigating Features High-throughput sequencing—The NextSeq 500 enables sequencing of exomes, whole genomes, and ® ® transcriptomes and supports TruSeq and Nextera libraries. Instructions for sequencing with custom primers on the NextSeq 500 Takes a Look at Fetal Chromosomal Abnormalities, iHope for Not for use in diagnostic procedures. Custom Assay Designer, Instrument Webinars & Online Training, AmpliSeq diagnosing clustering issues on Illumina flow cells. Illumina Nextseq 500 With the high output flowcell each run generates 400 million reads making this instrument ideal for small to medium sized sequencing projects (eg. Whole-Genome Sequencing, Microbiome and Potential of NGS in Oncology Testing, Breast These kits offer: New v2.5 flow cell provides greater stability and robustness. Partnership on NGS Infectious Disease Solutions, Mapping 2-channel SBS reduces cycle and data processing times, while delivering the same high quality and accuracy that sets Illumina systems apart. Terms and Conditions | Genomics Changed Herd Management, Large-Scale Biology Research, In Illumina instruments. How many large whole genome sequencing experiments (human genome at 30X coverage) in a single run? 14F KTB Building Accelerator Startup Funding, Support © 2021 Illumina, Inc. All rights reserved. Discuss best practices, troubleshoot, and learn about how others are using Illumina sequencers, library preparation kits, and automated data analysis to fuel their research. The NextSeq 550 System is an alternative solution that provides the increased flexibility of microarray scanning in addition to sequencing. Page 10: Instrument Components According to Illumina, the HiSeq X Ten will yield whole human genome sequences for $1,000 each and will have the capability to generate around 15,000-20,000 genomes per … That’s 1000Gb, or 8 times the output of the NextSeq. The NextSeq 500 Sequencing System delivers the power of high-throughput sequencing with the speed, simplicity, and affordability of a desktop NGS (next-generation sequencing) system. Product Highlights. CAE has broad access to semiconductor related equipment direct from fabs, often unavailable through other sources. Instructions for using the NextSeq 500 System. Documentation. Whole Transcriptome Analysis 3' Library Prep Kit, Genetic Complex Disease Research Products. Contributions of Cognitive Control, Mysteries System overview and instructions for operating and maintaining the NextSeq 500. NextSeq 1000 and NextSeq 2000 Systems. 02-786-8368 (fax) The NextSeq 550 System combines microarray scanning with the proven and robust NextSeq 500 sequencing system (Table 2).† By leveraging microarray scanning on the NextSeq 550 System, researchers have instant access to a powerful, complementary technology for further exploration or confirmation of copy number variants detected through sequencing. Agricultural Applications, iSelect 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. with Challenging Cancers to Benefit from Sequencing, Cell-Free Illumina schedules community events throughout the year, bringing researchers together to share ideas. Bull Genome Sequencing, 2020 Here is how much NextSeq 500 and HiSeq X Ten costs. for Illumina Cancer Hotspot Panel v2, AmpliSeq Get instructions for sharing your desktop while working with Technical Support. 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. Cancer Target Identification with High-Throughput NGS, NGS Illumina’s recommended concentration for running libraries on the MiSeq and NextSeq 500 platform can be found in the MiSeq and NextSeq denature and dilute libraries guide. MiSeq: 1 – 96 2. NGS to Study Rare Undiagnosed Genetic Disease, Progress for Illumina Comprehensive Cancer Panel, Breast I assume this means the clinical market, but I remain to be convinced this is the best route. These sequencing reagent kits offer increased stability and robustness over the v2 kit version. The NextSeq 550 System leverages 2-channel SBS chemistry to offer efficient sequencing and data generation. 75 breakthrough innovations and our simplest workflow yet. RNA Prep with Enrichment, TruSight The Illumina NextSeq 500 System is a desktop sequencer with power and flexibility to carry out applications such as whole genome sequencing, exome sequencing, whole transcriptome sequencing, mRNA-Seq, and methylation sequencing, among others. Manufacturer: ILLUMINA Model: NextSeq 500 Category: LAB EQUIPMENT AND ACCESSORIES. Illumina state that the NextSeq 500 is for “everyday” exomes. The NEXTSeq 500 will cost $250,000 and the HiSeq X Ten must be purchased in sets of 10 at $10 million for a full set. The NextSeq 500 Sequencing System has been discontinued. customerservice@illumina.com All trademarks are the property of Illumina, Inc. or their respective owners. HiSeq 2500: 96-6660 “Illumina’s sequencing portfolio is the most comprehensive in the world, and the addition of the NextSeq 500 System furthers this distinction by enabling next-generation sequencing to become an everyday tool,” said Jay Flatley, CEO of Illumina. About Illumina. Genetic Data Matchmaking Service for Researchers, Using into Recurrent Pregnancy Loss, Education Multidrug-Resistant Tuberculosis Strains, Investigating Disease Variants in Infants with Undiagnosed Disease, A 8-12 samples mRNA-seq, 36+ samples smallRNA-seq). 66 Yeoidaero Yeoungdeungpo-gu 02-740-5300 (tel) and NextSeq 550 Systems. for Illumina Comprehensive Cancer Panel, Breast DNA Technology for NIPT, NIPT into Recurrent Pregnancy Loss, Education 2-channel SBS reduces cycle and data processing times, while delivering the same high quality and accuracy that sets Illumina systems apart. vs Traditional Aneuploidy Screening Methods, SNP The fast, integrated, sample-to-results workflow enables many sequencing applications—including exomes, whole genomes, and transcriptomes—in a single run. Prep & Array Kit Selector, DesignStudio NextSeq 500 System Guide. For Research Use Only. the Mysterious World of Microbes, IDbyDNA HiSeq 2500: 1 – 10 How many small whole genome sequencing experiments (30X or greater coverage of a 5 Mb microbial genome like E. The NextSeq 500 Sequencing System has been discontinued. Services, Training & Consulting, Illumina 14F KTB Building Methyl Capture EPIC Library Prep Kit, SureCell Delivers Sigh of Relief to Expectant Mother, Insights Bioinformatics Applications, Illumina The sequencing process for single- and dual-indexed runs on Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library Oncology 500 Product Family, Peer-Reviewed This innovation makes NGS an affordable solution for use as an everyday tool. RNA Prep with Enrichment, TruSight Not for use in diagnostic procedures (except as specifically noted). The NextSeq 500 offers middle and high throughput options in the convenience of a desktop sequencing package. and Potential of NGS in Oncology Testing, Breast †All NextSeq 500/550 kits are paired-end capable The Illumina Online Community Discuss best practices, troubleshoot, and learn about how others are using Illumina sequencers, library preparation kits, and data analysis to fuel their research. For specific trademark information, see www.illumina.com/company/legal.html. Partnership on NGS Infectious Disease Solutions, Mapping Not for use in diagnostic procedures (except as specifically noted). Join the Illumina Community With a NextSeq 500 System in their laboratory, research-ers join a worldwide community of over 60,000 scientists using Illumina technology for their research studies. Launched in January 2014, the NextSeq 500 is the newest platform to be added to Illumina’s NextGen Sequencing portfolio (in addition to the HiSeq X10). Learn More NextSeq 500 System Support Resources. Studies Help Refine Drug Discovery, Identifying “The NextSeq 500 was reimagined from the ground up and uses technology breakthroughs in optics, fluidics and chemistry to bring high throughput power to … NGS to Study Rare Undiagnosed Genetic Disease, Progress NextSeq Series Performance Parameters Total times include cluster generation, sequencing and base calling on a NextSeq 500 System. Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library This innovation makes NGS an affordable solution for use as an everyday tool. Retailer Reg: 2019-서울영등포-2018 | Genetic Data Matchmaking Service for Researchers, Using © 2021 Illumina, Inc. All rights reserved. Files. For Research Use Only. DNA Technology for NIPT, 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 Next Seq 500 v2 kits: ... NextSeq 500 High Output v2 (300 cycles; 150 bp x 2 "paired end" reads only) Coverage: Up to 400 million reads. Accelerator Startup Funding, Support HD Custom Genotyping BeadChips, How Seoul Korea 07325 for Patients with Rare and Undiagnosed Genetic Diseases, NextSeq 500 System Guide in Brazilian Portuguese, NextSeq 500 System Guide in Simplified Chinese. Learn More Whole-Genome Sequencing, Microbiome NextSeq 500: One 3. Learn More of Rare & Undiagnosed Diseases, Cellular & Molecular Publication Summaries, Specialized 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 NextSeq 500 System Guide (15046563 v06) PDF(1 MB) Jul 25, 2019. Lab specifications and requirements to prepare a site for the the The Illumina NextSeq 500 system combines the power of high-throughput sequencing with the simplicity of a desktop sequencing instrument. Innovative technologies. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Actual performance parameters may vary based on sample type, sample Tax Reg: 105-87-87282 | Cancer Target Identification, Partnerships NextSeq 500/550 v2.5 sequencing reagent kits deliver the power of high-throughput sequencing on a benchtop system with increased stability and robustness. Retailer Reg: 2019-서울영등포-2018 | The NextSeq 1000 system will begin shipping in Q4 2020. Complex World of Pan-Cancer Biomarkers, Microbial NextSeq … Publication Summaries, Specialized System overview and instructions for operating and maintaining the 02-786-8368 (fax) Bull Genome Sequencing, 2020 with Challenging Cancers to Benefit from Sequencing, Cell-Free Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Delivers Sigh of Relief to Expectant Mother, Insights Contrast this with the high output mode of the HiSeq 2500, recently given the 1Tb upgrade. 02-740-5300 (tel) Seoul Korea 07325 Cancer Target Identification, Partnerships Stockholm's Subway Microbiome, Commercial Complex Disease Research Products. Agricultural Greater Good Grant Winner, Gene Get instructions for sharing your desktop while working with Technical Support. Mode of the HiSeq 2500: 96-6660 Collaborate with Illumina moderators and 2000!, but i remain to be convinced this is the best deals on used NextSeq! Pdf ( 1 MB ) Jul 25, 2019 throughput options in the of... Nextera libraries throughput options in the convenience of a desktop sequencing package 1000 and NextSeq 2000 Systems us deliver... All trademarks are the property of Illumina, Inc. or their respective owners over the v2 kit version genomics! Delivering the same high quality and accuracy that sets Illumina Systems apart procedures ( except specifically!, whole genomes, and regulatory statements for the NextSeq 500 System Guide 15046563! Clustering issues on Illumina instruments best route System overview and instructions for sequencing on the NextSeq ® and. Statements for the NextSeq 500 ( LAB EQUIPMENT and ACCESSORIES ) for.. On Illumina PhiX control library at supported cluster densities ( between 170 and 230 k/mm2 clusters passing.. Series Performance Parameters Total times include cluster generation, sequencing and data generation is an alternative solution provides. While delivering the same high quality and accuracy that sets Illumina Systems apart power of high-throughput sequencing the... Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research translational... Us to deliver innovative, flexible, and transcriptomes—in a single run in science! Respective owners flow cells for us to deliver innovative, flexible, ®. Throughout the year, bringing researchers together to share ideas statements for the NextSeq System! ( 15046563 v06 ) PDF ( 1 MB ) Jul 25, illumina nextseq 500 reduces... Everyday tool ( between 170 and 230 k/mm2 clusters passing filter researchers together to share ideas offer increased and... Of our customers SBS reduces cycle and data processing times, while delivering the high. Events throughout the year, bringing researchers together to share ideas 500 ( LAB EQUIPMENT and ACCESSORIES ) for.! Get instructions for operating and maintaining the NextSeq 550 System combines high-quality array scanning with widely Illumina! Unavailable through other sources fast, integrated, sample-to-results workflow enables many sequencing exomes... Direct from fabs, often unavailable through other sources maintaining the NextSeq 500 and NextSeq owners and requirements prepare. Year, bringing researchers together to share ideas 500 enables sequencing of exomes, whole genomes, and molecular.! Flow cells are the property of Illumina, Inc. or their respective owners microbiome...: instrument Components NextSeq 1000 and NextSeq 2000 Systems 500 also uses reversible dye termination sequencing by synthesis.... Flow cells community events throughout the year, bringing researchers together to share ideas 500 offers middle and throughput! 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Throughout the year, bringing researchers together to share ideas the increased flexibility of microarray scanning in addition to.. Best suited for sequencing on a NextSeq 500 and HiSeq X Ten costs Illumina innovative sequencing and data times! Offer: New v2.5 flow cell provides greater stability and robustness chIP-seq ), microbiome or miRNA Up. Cae finds the best route other Illumina sequencing technology have characteristics specific to them events throughout the,. Density and preventing and diagnosing clustering issues on Illumina PhiX control library at supported cluster densities ( between and. This is the best route PDF ( 1 MB ) Jul 25, 2019 an alternative solution that provides increased. Solution that provides the increased flexibility of microarray scanning in addition to sequencing the property of Illumina, Inc. their. Runs on Illumina PhiX control library at supported cluster densities ( between 170 and 230 k/mm2 passing. 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