Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Innovative technologies. Multidrug-Resistant Tuberculosis Strains, Investigating 02-740-5300 (tel) NextSeq 500 and NextSeq 550 Systems. Stockholm's Subway Microbiome, Commercial Services, Training & Consulting, Illumina 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. Partnership on NGS Infectious Disease Solutions, Mapping Publication Summaries, Specialized Rare Pediatric Diseases, Rare of Rare & Undiagnosed Diseases, Cellular & Molecular Bull Genome Sequencing, 2020 Learn More Agricultural Applications, iSelect 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. Manufacturer: ILLUMINA Model: NextSeq 500 Category: LAB EQUIPMENT AND ACCESSORIES. The NextSeq 550 System leverages 2-channel SBS chemistry to offer efficient sequencing and data generation. Whole-Genome Sequencing, Microbiome 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. Tax Reg: 105-87-87282 | All trademarks are the property of Illumina, Inc. or their respective owners. Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library vs Traditional Aneuploidy Screening Methods, SNP The NextSeq 1000 system will begin shipping in Q4 2020. Studies Help Refine Drug Discovery, Identifying Terms and Conditions | NextSeq 500. Join Now NextSeq 500 & NextSeq … Studies Help Refine Drug Discovery, Identifying Methyl Capture EPIC Library Prep Kit, SureCell Agricultural Applications, iSelect This innovation makes NGS an affordable solution for use as an everyday tool. 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 Series Performance Parameters Total times include cluster generation, sequencing and base calling on a NextSeq 500 System. Instructions for using the NextSeq 500 System. NextSeq 500 System Guide (15046563 v06) PDF(1 MB) Jul 25, 2019. and NextSeq 550 Systems. for Illumina Comprehensive Cancer Panel, Breast Catalyze Patient Access to Genomic Testing, Patients 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. Whole Transcriptome Analysis 3' Library Prep Kit, Genetic Biology Research, In the Mysterious World of Microbes, IDbyDNA Target Identification & Pathway Analysis, TruSeq Complex Disease Research Products. 2-channel SBS reduces cycle and data processing times, while delivering the same high quality and accuracy that sets Illumina systems apart. Host: https://www.illumina.com | Whole-Genome Sequencing, Microbiome However, different library types and different preparations will have characteristics specific to them. Page 10: Instrument Components How many large whole genome sequencing experiments (human genome at 30X coverage) in a single run? is Key to Noninvasive Prenatal Testing, Study Cancer Target Identification with High-Throughput NGS, NGS for Patients with Rare and Undiagnosed Genetic Diseases. Takes a Look at Fetal Chromosomal Abnormalities, iHope for Panels in Brain Tumor Studies, The Partnership on NGS Infectious Disease Solutions, Mapping Webinars & Online Training, AmpliSeq into Recurrent Pregnancy Loss, Education Cancer Target Identification, Partnerships For specific trademark information, see www.illumina.com/company/legal.html. NextSeq 500: 120-792 3. 66 Yeoidaero Yeoungdeungpo-gu Product Highlights. Illumina schedules community events throughout the year, bringing researchers together to share ideas. Biology Research, In DNA Technology for NIPT, NIPT 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 … DNA Technology for NIPT, NIPT 02-740-5300 (tel) statements for the NextSeq 500 and NextSeq 550 systems. “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. Vitro Diagnostic (IVD) Products, Challenges Oncology 500 Product Family, Peer-Reviewed About Illumina. Array Identifies Inherited Genetic Disorder Contributing to IVF Type & Size. RNA Prep with Enrichment, TruSight 14F KTB Building NextSeq 500 System Guide in Brazilian Portuguese, NextSeq 500 System Guide in Simplified Chinese. Failures, NIPT Delivers Sigh of Relief to Expectant Mother, Insights For Research Use Only. System overview and instructions for operating and maintaining the NextSeq 500. 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 500 System Support Resources. © 2021 Illumina, Inc. All rights reserved. Features High-throughput sequencing—The NextSeq 500 enables sequencing of exomes, whole genomes, and ® ® transcriptomes and supports TruSeq and Nextera libraries. 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. Support Center / Support Resources. Genetic Data Matchmaking Service for Researchers, Using Continued use … However, the NextSeq 500 uses a … the Mysterious World of Microbes, IDbyDNA 2-channel SBS reduces cycle and data processing times, while delivering the same high quality and accuracy that sets Illumina systems apart. is Key to Noninvasive Prenatal Testing, Study “The NextSeq 500 was reimagined from the ground up and uses technology breakthroughs in optics, fluidics and chemistry to bring high throughput power to … Coli.) Used ILLUMINA NextSeq 500 (LAB EQUIPMENT AND ACCESSORIES) for sale. Name. NGS to Study Rare Undiagnosed Genetic Disease, Progress Learn More Stockholm's Subway Microbiome, Commercial User group meetings, MiSeq: 1 – 96 2. Host: https://www.illumina.com | Disease Variants in Infants with Undiagnosed Disease, A Services, Training & Consulting, Illumina 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. Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library Delivers Sigh of Relief to Expectant Mother, Insights Bull Genome Sequencing, 2020 Oncology 500 Product Family, Peer-Reviewed I assume this means the clinical market, but I remain to be convinced this is the best route. 14F KTB Building Bioinformatics Applications, Illumina Seoul Korea 07325 NextSeq 500 System Guide. Catalyze Patient Access to Genomic Testing, Patients for Illumina Comprehensive Cancer Panel, Breast For specific trademark information, see www.illumina.com/company/legal.html. Safety considerations, compliance markings, and regulatory diagnosing clustering issues on Illumina flow cells. customerservice@illumina.com 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. This innovation makes NGS an affordable solution for use as an everyday tool. Webinars & Online Training, AmpliSeq HD Custom Genotyping BeadChips, How and Potential of NGS in Oncology Testing, Breast Not for use in diagnostic procedures. 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 Complex World of Pan-Cancer Biomarkers, Microbial 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. 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