in all RNA sample types, including FFPE. These sequencing reagent kits offer increased stability and robustness over the prior v2 kit version. of Rare & Undiagnosed Diseases, Cellular & Molecular Bull Genome Sequencing, 2020 Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project. Products for the NovaSeq 6000 System ... 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 A fast, user-friendly workflow for a wide range of target enrichment applications encompassing custom panels, fixed panels, and whole-exome sequencing. Use this tool to explore experimental sequencing library preparation methods compiled from the scientific literature. Services, Training & Consulting, Peer-Reviewed
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A laboratory information management system that helps labs track samples and optimize procedures and workflows. 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. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Perform transcriptome profiling for hundreds to tens of thousands of single cells in one experiment. © 2020 Illumina, Inc. All rights reserved.
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. Terms and Conditions | Complex Disease Research, TruSeq 02-786-8368 (fax) NGS to Study Rare Undiagnosed Genetic Disease, Progress Whole Transcriptome Analysis 3' Library Prep Kit, Genetic
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NGS to Study Rare Undiagnosed Genetic Disease, Progress Interrogate over 850,000 methylation sites quantitatively across the genome at single-nucleotide resolution. Search Products by Name or Category ID Search. View a complete list of Illumina sequencing and microarray products. bacterial and viral genomes), amplicons, and plasmids. Genomics Changed Herd Management, Large-Scale This is the international website for Illumina.
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HD Custom Genotyping BeadChips, How 66 Yeoidaero Yeoungdeungpo-gu Rapid library preparation from a broad range of sample types for studying the coding and non-coding transcriptome with unparalleled study flexibility. AmpliSeq for Illumina is a suite of AmpliSeq chemistry products that are compatible with Illumina next-generation sequencing platforms. Delivers Sigh of Relief to Expectant Mother, Insights Better Buy: Illumina vs. Adaptive Biotechnologies One company has a well-established line of products that made it the leader in its niche, but the other has a bold vision about how to use them. The fast and simple protocol allows for treatment of one or a pool of libraries just prior to sequencing on any Illumina platform.
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. for Illumina Cancer Hotspot Panel v2, AmpliSeq Find featured Illumina products, as well as customer favorites. Publication Summaries, Specialized
vs Traditional Aneuploidy Screening Methods, SNP Comprehensive panels targeting disease-associated regions of the exome All trademarks are the property of Illumina, Inc. or their respective owners. Methyl Capture EPIC Library Prep Kit, SureCell Agricultural Greater Good Grant Winner, 2019 © 2020 Illumina, Inc. All rights reserved.
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Optimized chemistry to increase cluster density and read length, and improve sequencing quality scores, compared to earlier MiSeq reagent kit versions. Takes a Look at Fetal Chromosomal Abnormalities, iHope Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Prep & Array Kit Selector, DesignStudio vs Traditional Aneuploidy Screening Methods, SNP All trademarks are the property of Illumina, Inc. or their respective owners. is Key to Noninvasive Prenatal Testing, Study Host: https://www.illumina.com | Products.
It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers ... and providing the highest level of quality, we strive to meet this challenge.
Whole-Genome Sequencing, Microbiome 02-740-5300 (tel) Identify genetic associations with common and rare traits across diverse populations. Panels in Brain Tumor Studies, TruSight Immune profiling of human tumors identifies CD73 as a combinatorial target in glioblastoma, FDA amendment leverages the power of various Illumina sequencers for COVID-19 testing, A sequencing lab case study on accelerated bioinformatics, Empower the journey from association to causality, All Oncology 500 Product Family, AmpliSeq Retailer Reg: 2019-서울영등포-2018 | For Research Use Only. Products / Browse by Product Type / Sequencing Kits / Library Preparation Kits / Illumina Stranded Total RNA Prep with Ribo-Zero Plus Limited-Time Offer: Save 25% Use code RNA25 at checkout to receive 25% off your first order of Illumina Stranded Total RNA with Ribo-Zero Plus, now through the end of 2020. Multidrug-Resistant Tuberculosis Strains, eDNA It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. 66 Yeoidaero Yeoungdeungpo-gu Prep & Array Kit Selector, DesignStudio Genomics Products for Genetic Diseases Sequencing and microarray solutions to advance breakthroughs in rare and genetic diseases. with Challenging Cancers to Benefit from Sequencing, Cell-Free These reagents offer increased stability and robustness over the v2 kit version. Perform targeted genotyping on large numbers of samples. Device Designation for Illumina TruSight Assay, SNP Contributions of Cognitive Control, Mysteries Methyl Capture EPIC Library Prep Kit, SureCell Oncology 500 to Power Liquid Biopsy Studies, Microbial
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75 breakthrough innovations and our simplest workflow yet, Reagent kits for the NovaSeq 6000 System provide ready-to-use cartridge-based reagents for cluster generation and SBS, Compare instruments and find one that's right for you, Higher accuracy in somatic, structural variant, and RNA pipelines, while maintaining computation speed, Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing, Find popular product groupings for your workflow, Whole-genome sequencing has the potential to shorten diagnostic odysseys, Data from severely ill patients may help us understand genetics of susceptibility, Procedure for novel coronavirus (2019-nCoV), Gain a high-resolution view of both coding and noncoding RNA for a deeper understanding of biology, A culture-free method for studying complex microbiomes or environments, Contributing to a sustainable environment and food supply, Learn how these scores can shape the future understanding of disease risk and mitigation, All 14F KTB Building Not for use in diagnostic procedures (except as specifically noted).
Products to support workflows and emerging applications Explore kits, services, and software solutions for the NextSeq 1000 and NextSeq 2000 ... Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Custom Assay Designer, Instrument
All trademarks are the property of Illumina, Inc. or their respective owners. 02-740-5300 (tel) is Revealing the Mysterious World of Microbes, Commercial It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers.
Cancer Target Identification with High-Throughput NGS, NGS For specific trademark information, see www.tst-web.illumina.com/company/legal.html. If you are looking for information specific to your region, please select your location and we will redirect you. burden (TMB) and microsatellite instability (MSI), even from
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