540 Mb15 Gb output range . No. NovaSeq 6000 System; All Agrigenomics Products. With Nextera technology, DNA is simultaneously fragmented and tagged with sequencing adapters in a single step, using standard lab equipment. Transcriptome Analysis (samples per run, dual flow cell): S1: 128, S2: 256, S4: 768. Analyze circulating tumor DNA from plasma with the TruSight Oncology 500 ctDNA assay. For whole-genome sequencing. This kit uses a fast, user-friendly workflow. The HiSeq X Ten empowers scientists, institutions, and nations to create a comprehensive catalog of human and species variation, forge population-based references, drive far-reaching discoveries, and advance the study of cancer and complex diseases at a record pace. Select and sequence polyadenylated transcripts for gene expression profiling studies. How Genomics Will Support Gorilla Conservation. 2022 Illumina, Inc. All rights reserved. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Orleans county fair 2022 vermont The fair kicks off with Scotty McCreery, Friday, August 26 th, Nelly, Saturday, August 27 th and a Monster Truck Show Sunday, August 28 th. Share With Tech Support. & Pipeline Setup, Sequencing Data Samples prepared with Nextera kits are compatible with all Illumina sequencers. 20041797). Featured Products. This results in economical, high-throughput RNA sequencing studies achieved with a user-friendly workflow. Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information. Total time includes cluster generation, sequencing, and base calling on a NextSeq 550 System enabled with dual-surface scanning. kanni theme. 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. Explore the breakthroughs, advancements, and progress. *When used at scale, the HiSeq X Ten delivers a $1000 genome, inclusive of instrument depreciation, DNA extraction, library preparation, and estimated labor for a typical high-throughput genomics laboratory. It is a required accessory instrument for HiSeq sequencers. Software Suite, BaseSpace The HiSeq X Ten System was purpose-built for population-scale WGS. On-bead tagmentation chemistry is combined with a simplified, single hybridization protocol to reduce total workflow time. Nextera DNA kits provide a fast and easy library prep workflow, delivering whole-genome sequencing libraries in under 90 min. Not for use in diagnostic procedures (except as specifically noted). Host: https://www.illumina.com | DNA Sequencing RNA Sequencing Methylation Sequencing Library Preparation High-Throughput Sequencing. 2 100 bp 2 100 bp Learn More. This program is available for a limited time only. 1.6B - 40B. BaseSpace NovaSeq 6000IlluminaSBSDNA . Enable comprehensive genomic profiling with accurate and comprehensive homologous recombination deficiency assessment, Discover novel trait and disease associations with optimized tag SNPs and functional exonic content at an attractive price, All Software & Informatics The HiSeq X Ten System is the worlds first to break the $1000 genome barrier for human whole-genome sequencing (WGS). FEATURED PRODUCTS. The Illumina HiSeq X instrument is being displayed as an example of how sequencing technology is helping amass the data in the 100,000 Genomes Project, allowing scientists to do pioneering research. & Pipeline Setup, Sequencing Data Tax Reg: 105-87-87282 | 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 NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab. 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. Learn More. Software Suite, BaseSpace For specific trademark information, see www.illumina.com/company/legal.html. The NovaSeq 6000 System combines benchtop sequencer ease of use with production-scale power in a single platform, with adjustable data output for maximum efficiency. Run time. Output per Flow Cell for Various Read Lengths * NovaSeq 6000 System. Technical Support. Remove rRNA from plant leaf, seed, and root tissue. Software Suite, BaseSpace System Specifications . Content Specifications: Captures Methylation analysis and RNA-Seq are helping researchers understand how endurance training makes epigenetic changes to the human genome. A quality score (Q-score) is a prediction of the probability of an error in base calling. The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab. Kits include SBS reagents, clustering reagents, and patterned flow cells for increased cluster density and simplified image analysis, compared to non-patterned flow cells. Discover how HiSeq X Ten breaks the $1000 genome barrier for human whole-genome sequencing. Rapid library preparation from a broad range of sample types for studying the coding and non-coding transcriptome with unparalleled study flexibility. Bio-IT Platform, TruSight 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. Compared to current methods for preparing mRNA samples for sequencing, use of the TruSeq reagents significantly reduces the number of steps and hands-on time. NGS enables fast, accurate characterization of any species. The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab. Enable comprehensive genomic profiling with accurate and comprehensive homologous recombination deficiency assessment. For specific trademark information, see www.illumina.com/company/legal.html. This innovation makes NGS an affordable solution for use as an everyday tool. BaseSpace RNA-Seq uses next-generation sequencing to analyze expression across the transcriptome, enabling scientists to detect known or novel features and quantify RNA. Analyze both coding RNA and multiple forms of noncoding RNA for a comprehensive view of the transcriptome. 5.36 billion reads per run . Customer Dashboard, Infrastructure SBS kanni theme. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. | Based on 10 million reads. Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. All trademarks are the property of Illumina, Inc. or their respective owners. Increase chances of finding a positive biomarker by moving from individual biomarker assays to a single comprehensive NGS assay, Go from initial sample to results in 4-5 days. Content Specifications: Targeted selection of DNA from 523 genes of interest, and RNA from 55 genes, for a total of 1.94Mb panel size. Retailer Reg: 2019--2018 | Collaborate with Illumina moderators, customers, and developers. 7 versions, DRAGEN TruSight Oncology 500 Analysis Software v1.1 Documentation, TruSight Oncology 500 v1.0 Local App Documentation, TruSight Oncology 500 v2.0 Local App Documentation, TruSight Oncology 500 v2.1 Local App Documentation, DRAGEN TruSight Oncology 500 Analysis Software v2.1 Documentation, DRAGEN TruSight Oncology 500 Analysis Software v1.1 on ICA Documentation, TruSight Oncology 500 Support Documentation, TruSight Oncology 500 v2.2 Local App Documentation, AllTruSight Oncology 500 ** Install specifications based on Illumina PhiX control library at supported cluster densities (865-965 k/mm 2 clusters passing filter for v2 chemistry and 1200-1400 k/mm 2 clusters passing filter for v3 chemistry). Sequence Hub, BaseSpace Host: https://www.illumina.com | Nextera Library Validation and Cluster Density Optimization, Illumina Experiment Manager User Guide Documentation, Nextera DNA Library Prep Checklist Documentation, Nextera DNA Sample Preparation Product Insert Documentation, Nextera DNA Library Prep Consumables and Equipment Documentation, Nextera DNA Library Prep Kit Documentation, Nextera DNA Library Prep Reference Guide Documentation, Custom Protocol SelectorGenerates customized, end-to-end instructions, AllNextera DNA Library Prep Kit 7-25 million reads per run . Customer Dashboard, Infrastructure Consolidate Multiple Biomarker Assays into One, Enable In-House Comprehensive Genomic Profiling. Price . *Specifications based on Illumina PhiX control library at supported cluster densities. Variant detection sensitivity and biases in whole genome and exome sequencing. Analysis, Biological Data Find an up-to-date list of automation vendors with robotic systems compatible with this kit. Intended Use for the NextSeq 550Dx. Apps, DRAGEN Researchers develop novel sequencing methods with the MiSeq and HiSeq Systems to understand the epigenome and its impact on cancer and immune diseases. Scientists are combining genomics, transcriptomics, epigenetics, and proteomics to unlock discovery power not found through single omics approaches. See how you can use multiomics to gain a multidimensional view of cells and complex biological systems. Paired-end sequencing enables both ends of the DNA fragment to be sequenced. Specifications and individual lot data from the tests that are performed for this particular product can be found and downloaded on the Product Specification Sheet, Certificate of Analysis, data card or product manual. The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab. A quality score (Q-score) is a prediction of the probability of an error in base calling. TruSight Oncology 500 HRD* is an optional add-on kit to TruSight Oncology 500 and enables detection of homologous recombination deficiency (HRD) through assessment of a genomic instability score (GIS). Analysis, Biological Data Customer Stories. Based on 25 million reads. 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. Easily translate raw data into a final interpretation report, powered by Pierian Clinical Genomics Workspace (CGW) software. The MiSeq System offers a DNA-to-results sequencing solution with a small footprint that fits into virtually any lab environment. All three TruSight Oncology 500 assays are designed to identify key biomarkers in guidelines and clinical trials. The 10 instruments of a HiSeq X Ten System generate a staggering level of throughput for processing tens of thousands of samples. Whole-genome sequencing delivers a comprehensive view, ideal for discovery applications. * The product to evaluate DNA & RNA variants is the TruSight Oncology 500 DNA/RNA Bundle. NovaSeq 6000 System; All Agrigenomics Products. NovaSeq 6000 System; All Agrigenomics Products. 2 250 bp max read length. Products iScan Products iSeq 100 Products MiniSeq Products MiSeq Products MiSeqDx Products NextSeq 500 & NextSeq 550 Products NovaSeq 6000 Products NextSeq 1000 & 2000 Products. Products, DRAGEN v4.0 release enables machine learning by default, providing increased accuracy out of the box, Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing, Whole-exome sequencing kit with library prep, hybridization reagents, exome probe panel, size selection beads, and indexes, See what is possible through the latest advances in high-throughput sequencing technology, View the unveiling of our newest technologies and products on-demand, recorded live at the Illumina Genomics Forum, Get instructions for using Illumina DRAGEN Bio-IT Platform v4.0, A campus lab sequences dust from vacuum bags to understand the variants and viral load of SARS-CoV-2 and other viruses, Mapping genetic diversity to identify where confiscated gorillas come from and boost survival rates, Explore the advantages of NGS for analysis of gene expression, gene regulation, and methylation, The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab. Generate mRNA-focused sequencing libraries from total RNA, with enhanced multiplex capability and a simple workflow with master-mixed reagents. Guideline Coverage: Broad coverage of key guidelines for multiple solid tumor types NovaSeq 6000: NovaSeq 6000: The Nextera DNA Flex Library Prep Kit is ideally suited to a wide range of whole-genome sequencing applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species. The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab. Sequence Hub, BaseSpace Pricing & Specifications Pricing; Specifications; Select Product(s) Price. Rapid variant calling algorithm powered by DRAGEN Bio-IT Platform, available for TruSight Oncology 500 locally on DRAGEN Server and coming soon via secure, cloud based analysis with Illumina Connected Analytics (ICA). Learn More. The technological advancements provided by the HiSeq X Series change the economics of variant detection, driving price parity between whole-exome and whole-genome sequencing for variant detection in exonic regions. Method-Specific Workflow Example . BMC Bioinformatics. De novo sequencing refers to sequencing a novel genome with no reference sequence available. Capture a comprehensive view of the plant transcriptome with this RNA-Seq library prep workflow. 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. TruSight Oncology 500 HRD available now. PDF | Apps, DRAGEN Join other Illumina customers in the Illumina Online Community. This allows the samples to be pooled and then individually identified during downstream analysis. All NextSeq 550 kits are paired-end capable. Best Practices for Storing Sequencing Reagents. NovaSeq X series specifications. 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. Provides comprehensive gene fusion detection in formalin-fixed, paraffin-embedded (FFPE) and other cancer research samples. A set of NGS platform reagents for detecting cancer variants, using an enrichment-based method to simultaneously analyze DNA and RNA. Analysis, Biological Data A simple PCR amplification then appends sequencing adapters and sample indexes to each fragment. WGS also provides greater coverage uniformity and higher sensitivity at lower depths of coverage compared to exome sequencing.1. 2022 Illumina, Inc. All rights reserved. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Not for import or sale to the Australian general public. The NextSeq 550 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. All trademarks are the property of Illumina, Inc. or their respective owners. Products, DRAGEN v4.0 release enables machine learning by default, providing increased accuracy out of the box, Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing, Whole-exome sequencing kit with library prep, hybridization reagents, exome probe panel, size selection beads, and indexes, See what is possible through the latest advances in high-throughput sequencing technology, View the unveiling of our newest technologies and products on-demand, recorded live at the Illumina Genomics Forum, Get instructions for using Illumina DRAGEN Bio-IT Platform v4.0, A campus lab sequences dust from vacuum bags to understand the variants and viral load of SARS-CoV-2 and other viruses, Mapping genetic diversity to identify where confiscated gorillas come from and boost survival rates, Explore the advantages of NGS for analysis of gene expression, gene regulation, and methylation, The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab, TruSeq RNA Library Preparation Kit v2, Set A (48 samples, 12 indexes), TruSeq RNA Library Preparation Kit v2, Set B (48 samples, 12 indexes), Get more from your core: RNA-Seq techniques in action. Generate whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA. & Pipeline Setup, Sequencing Data Not for import or sale to the Australian general public. Meynert AM, Ansari M, FitzPatrick DR, Taylor MS. If you are planning to sequence your samples on any instrument other than the NovaSeq 6000 System, you'll need to purchase the Illumina DNA PCR-Free Sequencing and Indexing Primer (Cat. DRAGEN v3.10 release now available, setting new standards for accuracy and increased genome coverage. Contact Us. Sequence Hub, BaseSpace Fill out | Not for import or sale to the Australian general public. Performs alignment, quantification, and fusion detection. Interpretation, Certificates (CofC, CofA) and Master Lot Sheets, AmpliSeq for Illumina Cancer Hotspot Panel v2, AmpliSeq for Illumina Comprehensive Cancer Panel, Breast Cancer Target Identification with High-Throughput NGS, The Complex World of Pan-Cancer Biomarkers, Microbiome Studies Help Refine Drug Discovery, Identifying Multidrug-Resistant Tuberculosis Strains, Investigating the Mysterious World of Microbes, IDbyDNA Partnership on NGS Infectious Disease Solutions, Infinium iSelect Custom Genotyping BeadChips, 2020 Agricultural Greater Good Grant Winner, 2019 Agricultural Greater Good Grant Winner, Gene Target Identification & Pathway Analysis, TruSeq Methyl Capture EPIC Library Prep Kit, Genetic Contributions of Cognitive Control, Challenges and Potential of NGS in Oncology Testing, Partnerships Catalyze Patient Access to Genomic Testing, Patients with Challenging Cancers to Benefit from Sequencing, NIPT vs Traditional Aneuploidy Screening Methods, SNP Array Identifies Inherited Genetic Disorder Contributing to IVF Failures, NIPT Delivers Sigh of Relief to Expectant Mother, Education is Key to Noninvasive Prenatal Testing, Study Takes a Look at Fetal Chromosomal Abnormalities, Rare Disease Variants in Infants with Undiagnosed Disease, A Genetic Data Matchmaking Service for Researchers, Using NGS to Study Rare Undiagnosed Genetic Disease, Progress for Patients with Rare and Undiagnosed Genetic Diseases, > 75% bases higher than Q30 at 2 150 bp. Software Suite, BaseSpace With the NovaSeq X Plus system, you can sequence over 1000 transcriptomes in a single run using a dual 25B flow cell run. The Illumina Free Adapter Blocking Reagent is an optional reagent that can be used to treat most types of sequencing libraries to reduce index hopping levels. Learn More. Capture genomic regions of interest via hybridization to target-specific biotinylated probes. For specific trademark information, see www.illumina.com/company/legal.html. Custom Protocol Selector. Max read length. 2022 Illumina, Inc. All rights reserved. Batch up to 192 samples at a time while using the same biomarkers and tissue type as the TruSight Oncology 500 assay. NovaSeq 6000 Reagent Kits v1.5. Retailer Reg: 2019--2018 | Support. Featured Products. Specifications. Visit Champlainvalleyfair.org for tickets and pricing.. The MiSeq System harnesses proven Illumina SBS technology to deliver highly accurate data and robust performance for a broad range of applications. Tools View All. Investigate a number of high-throughput applications that can be run on the HiSeq Series. Learn More. 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. Retailer Reg: 2019--2018 | Not for use in diagnostic procedures (except as specifically noted). For specific trademark information, see emea.illumina.com/company/legal.html. We are proud to help make your research more affordable. Retailer Reg: 2019--2018 | Host: https://www.illumina.com | Not available in the US or Japan. /4000, or HiSeq X, you may be eligible to trade in your existing instrument for a new NovaSeq 6000 System. Retailer Reg: 2019--2018 | 2 150 bp max read length. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers.