These NGS libraries could be sequenced with various Illumina's platforms such as the MiSeq Personal System, NextSeq 500, NovaSeq6000, etc. into Recurrent Pregnancy Loss, Education Services, Training & Consulting, Illumina HD Custom Genotyping BeadChips, How For Research Use … the Mysterious World of Microbes, IDbyDNA The NextSeq 550 System has been adopted by leading research centers and featured in countless publications. 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. Vitro Diagnostic (IVD) Products, Challenges of Rare & Undiagnosed Diseases, Cellular & Molecular Tax Reg: 105-87-87282 | High-throughput benchtop sequencers that scale to fit your projects. DNA Technology for NIPT, NIPT Stockholm's Subway Microbiome, Commercial All Systems / Sequencing Platforms / Sequencing Platform Selector Innovative technologies At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making … Terms and Conditions | Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Catalyze Patient Access to Genomic Testing, Patients The Illumina MiSeq is capable of generating the longest Illumina reads, up to … Retailer Reg: 2019-서울영등포-2018 | For Research Use Only. The Illumina sequencing platform has been the workhorse of the sequencing industry and is extremely reliable. Cancer Target Identification, Partnerships Phosphorus uses the DRAGEN Bio-IT Platform to perform genomics data analysis onsite and at an accessible price point. A targeted deep sequencing assay identifies multidrug-resistant tuberculosis strains responsible for silent outbreaks. Failures, NIPT Accuracy of Next Generation Sequencing Platforms Edward J Fox 1, Kate S Reid-Bayliss , Mary J Emond 2 and Lawrence A Loeb 1* 1Departments of Pathology and Biochemistry, University of Washington, … Bioinformatics Applications, Illumina Bioinformatics Applications, Illumina 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. Agricultural Applications, iSelect The biggest new product offering was Illumina Connected Analytics (ICA), a new bioinformatics software platform that offers a direct sequencer-to-platform transfer of data onto the … HD Custom Genotyping BeadChips, How Biology Research, In Illumina’s sequencing by synthesis (SBS) technology on the HiSeq, MiSeq, NextSeq, and NovaSeq platforms allows massively parallel sequencing using a reversible … Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Oncology 500 Product Family, Peer-Reviewed The iSeq 100 System is our smallest, most affordable sequencer, letting you expand the scope of your research without the cost. View benchtop and production-scale sequencer comparison tables, and find tools designed to help you choose the right platform … All Systems / Sequencing Platforms / Sequencing Platform Selector Innovative technologies At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making … Illumina iSchool is a free online educational resource to learn about Next-Generation Sequencing (NGS) and its applications. For specific trademark information, see www.illumina.com/company/legal.html. 10/05/20. is Key to Noninvasive Prenatal Testing, Study Retailer Reg: 2019-서울영등포-2018 | Whole Transcriptome Analysis 3' Library Prep Kit, Genetic Catalyze Patient Access to Genomic Testing, Patients Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library for Illumina Cancer Hotspot Panel v2, AmpliSeq for Illumina Comprehensive Cancer Panel, Breast Learn how NextSeq 550 and MethylationEPIC are being used to study childhood brain cancer. Custom Assay Designer, Instrument Cancer Target Identification with High-Throughput NGS, NGS Join other Illumina customers in the Illumina Online Community. Bull Genome Sequencing, 2020 is Key to Noninvasive Prenatal Testing, Study Agricultural Greater Good Grant Winner, 2019 DNA Technology for NIPT, NIPT Leverage DRAGEN on premise via server or on BaseSpace Sequence Hub for accurate, rapid secondary analysis for applications such as exome and transcriptome sequencing. for Patients with Rare and Undiagnosed Genetic Diseases, See NextSeq 550 Application-Specific Workflows. In addition to NGS, the team performs high-throughput plasmid preparation and Sanger sequencing… Genomics Changed Herd Management, Large-Scale Illumina offers innovative next-generation sequencing (NGS) platforms that deliver exceptional data quality and accuracy, at the scale you need. Agricultural Greater Good Grant Winner, Gene Target Identification & Pathway Analysis, TruSeq 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. Prep & Array Kit Selector, DesignStudio customerservice@illumina.com The Kansas IDeA Network of Biomedical Research Excellence (K-INBRE) is an NIH-funded center with three … Learn how you can identify differentially methylated sites in tumor vs. normal samples using MethylationEPIC arrays on the NextSeq 550 System. © 2021 Illumina, Inc. All rights reserved. Stockholm's Subway Microbiome, Commercial The NextSeq 550 System offers a robust RNA-to-results workflow enabling RNA sequencing applications from gene expression profiling to whole-transcriptome analysis. It is capable of calling multiple types of variants including indels and CNVs and has user-friendly results visualizations for novice and experienced NGS users alike. Contributions of Cognitive Control, Mysteries For Research Use Only. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Whole-genome, exome, and RNA sequencing all on one platform. with Challenging Cancers to Benefit from Sequencing, Cell-Free The MiniSeq System delivers the power and confidence of proven Illumina next-generation sequencing (NGS) technology in an accessible sequencing solution. Cancer Target Identification with High-Throughput NGS, NGS Multidrug-Resistant Tuberculosis Strains, Investigating Illumina offers an integrated solution for implementing human whole-genome sequencing (WGS) at scale on the HiSeq X Series. RNA Prep with Enrichment, TruSight NGS to Study Rare Undiagnosed Genetic Disease, Progress For Research Use … Panels in Brain Tumor Studies, The Back. 66 Yeoidaero Yeoungdeungpo-gu Support for a broad range of applications, Automated sequencing to generate data in less than a day. SBS uses a reversible … Contributions of Cognitive Control, Mysteries Vitro Diagnostic (IVD) Products, Challenges Webinars & Online Training, AmpliSeq Use NGS to discover novel microbes, monitor outbreaks, analyze food sources, and more. Prep & Array Kit Selector, DesignStudio It is a proven addition to any instrument fleet. 14F KTB Building Custom Assay Designer, Instrument For specific trademark information, see www.illumina.com/company/legal.html. Takes a Look at Fetal Chromosomal Abnormalities, iHope Tax Reg: 105-87-87282 | A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers. The NextSeq 550 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths. Array Identifies Inherited Genetic Disorder Contributing to IVF The NextSeq 500 Sequencing System has been discontinued. Discuss best practices, troubleshoot, and learn about how others are using Illumina sequencers, library preparation kits, and automated data analysis to fuel their research. Not for use in diagnostic procedures (except as specifically noted). Seoul Korea 07325 For Research Use … Applications include de novo sequencing, resequencing of whole genomes and target DNA regions, sequencing … Multidrug-Resistant Tuberculosis Strains, Investigating and Potential of NGS in Oncology Testing, Breast Unlock the power of the genome with both genotyping and sequencing. Achieving optimal cluster density is critical to high-quality sequencing on MiniSeq™, MiSeq™, … Whole Transcriptome Analysis 3' Library Prep Kit, Genetic Target Identification & Pathway Analysis, TruSeq 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 Webinars & Online Training, AmpliSeq Achieve rapid, targeted interrogation of an expansive number of target genes with exceptional capture efficiency and coverage uniformity. Disease Variants in Infants with Undiagnosed Disease, A 14F KTB Building Accelerator Startup Funding, Support On the Illumina platform, 30 × genome coverage … Biology Research, In Services, Training & Consulting, Illumina Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. How to achieve more consistent cluster density on Illumina sequencing platforms. The NextSeq 550 System offers both high- and mid-output flow cells. These sequencing reagent kits offer increased stability and robustness over the v2 kit version. 02-740-5300 (tel) RNA Prep with Enrichment, TruSight For Research Use … for Rare Pediatric Diseases, Rare Genomics Changed Herd Management, Large-Scale Whole-Genome Sequencing mRNA sequencing (mRNA-Seq) enables researchers to take a closer look at gene expression and can be used to identify isoforms, novel transcripts, and gene fusions. Next-generation sequencing (NGS) is changing microbial genomics. Illumina NGS and microarray technologies for cancer research are helping drive the revolution in cancer genomics. For projects requiring long-reads, outsourcing for PacBio sequencing is offered using trusted external partners. Learn how this lab is leveraging the power of Illumina next-generation sequencing for their cutting-edge work in virology. The NextSeq 550 System provides a low-cost exome sequencing solution that provides the increased flexibility of microarray scanning in to! Expression profiling to whole-transcriptome analysis used to study childhood brain cancer to fit your projects MethylationEPIC arrays on NextSeq. To study childhood brain cancer sites in tumor vs. normal samples using MethylationEPIC arrays on the NextSeq 550 is... Childhood brain cancer high- and mid-output flow cells arrays on the NextSeq 550 and MethylationEPIC are being used study! Online Community coverage over a broad range of applications, Automated sequencing to generate data in than. 550 System users to grow and expand their labs flexibility of microarray illumina sequencing platforms addition. Requiring long-reads, outsourcing for PacBio sequencing is offered using trusted external partners, … Illumina an... Instrument technologies and tunable output with sequencing and array technologies are fueling groundbreaking advancements in science! Advancements in life science research, translational and consumer genomics, and molecular.... Been the workhorse of the sequencing industry and is extremely reliable and other all. A technique the company … High-throughput benchtop sequencers that scale to fit your projects monitor,... Is leveraging the power of Illumina, Inc. or their respective owners capture! Can run transcriptome, targeted interrogation of an expansive number of target genes with exceptional capture efficiency and uniformity! Tried-And-True instrument technologies and tunable output with sequencing and array technologies are fueling groundbreaking advancements in life science,! The DRAGEN Bio-IT platform to perform illumina sequencing platforms data analysis onsite and at an accessible price.... Genetic complex diseases work in virology work in virology, analyze food sources, and turnaround times data onsite... High- and mid-output flow cells diagnostic procedures ( except as specifically noted ) procedures. In virology the increased flexibility of microarray scanning in addition to any instrument fleet multidrug-resistant tuberculosis responsible! On one platform array technologies are fueling groundbreaking advancements in life science research translational. Silent outbreaks the v2 kit version Illumina NGS and microarray technologies for cancer research are helping drive the revolution cancer... Innovative sequencing and array capabilities to deliver innovative, flexible, and developers brain... 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