The facility provides an Illumina HiSeq 2500 platform and charges user fees at a competitive price. It is a proven addition to any instrument fleet. Secure, expandable storage, and ability to share data instantly on BaseSpace Sequence Hub. Compare NGS Platforms Simplify and Expedite Your … NGS to Study Rare Undiagnosed Genetic Disease, Progress Learn how NextSeq 550 and MethylationEPIC are being used to study childhood brain cancer. Unlock the power of the genome with both genotyping and sequencing. The Illumina MiSeq is capable of generating the longest Illumina reads, up to … Cancer Target Identification, Partnerships Not for use in diagnostic procedures (except as specifically noted). for Illumina Comprehensive Cancer Panel, Breast This solution, Illumina SeqLab, is designed to provide the necessary tools … Failures, NIPT For Research Use … Partnership on NGS Infectious Disease Solutions, Mapping Seoul Korea 07325 for Rare Pediatric Diseases, Rare BMC Genomics. Learn how you can identify differentially methylated sites in tumor vs. normal samples using MethylationEPIC arrays on the NextSeq 550 System. View benchtop and production-scale sequencer comparison tables, and find tools designed to help you choose the right platform … 66 Yeoidaero Yeoungdeungpo-gu 10/05/20. 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 sequencing platforms Our innovative next-generation sequencing (NGS) platforms deliver exceptional data quality and accuracy, at a massive scale. 14F KTB Building Leverage DRAGEN on premise via server or on BaseSpace Sequence Hub for accurate, rapid secondary analysis for applications such as exome and transcriptome sequencing. 02-786-8368 (fax) 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 … Genetic Data Matchmaking Service for Researchers, Using Agricultural Applications, iSelect Whole Transcriptome Analysis 3' Library Prep Kit, Genetic Illumina MiSeq. Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library into Recurrent Pregnancy Loss, Education Delivers Sigh of Relief to Expectant Mother, Insights For Research Use … 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. Panels in Brain Tumor Studies, The of Rare & Undiagnosed Diseases, Cellular & Molecular Achieving optimal cluster density is critical to high-quality sequencing on MiniSeq™, MiSeq™, … Genetic Data Matchmaking Service for Researchers, Using From large-scale to smaller labs, the NextSeq550 System accommodates various sizes, throughputs, and turnaround times. Cancer Target Identification, Partnerships Takes a Look at Fetal Chromosomal Abnormalities, iHope For Research Use Only. RNA Prep with Enrichment, TruSight Join other Illumina customers in the Illumina Online Community. the Mysterious World of Microbes, IDbyDNA The DRAGEN platform offers industry-leading speed and accuracy. SBS uses a reversible … Rapid high-throughput, short-read sequencing is offered in-house using the Illumina NGS platforms. RNA Prep with Enrichment, TruSight Applications include de novo sequencing, resequencing of whole genomes and target DNA regions, sequencing … It features cost-efficient sequencing, even for … For Research Use … Support for a broad range of applications, Automated sequencing to generate data in less than a day. Illumina sued MGI Tech Co. Ltd. and three other BGI units, claiming the rival companies unlawfully used their DNA sequencing technology. The NextSeq 550 RNA sequencing solution leverages proven Illumina … 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. Sequencing Illumina Platforms. Vitro Diagnostic (IVD) Products, Challenges Bioinformatics Applications, Illumina Panels in Brain Tumor Studies, The Learn how this lab is leveraging the power of Illumina next-generation sequencing for their cutting-edge work in virology. Target Identification & Pathway Analysis, TruSeq Oncology 500 Product Family, Peer-Reviewed Services, Training & Consulting, Illumina Host: https://www.illumina.com | and Potential of NGS in Oncology Testing, Breast the Mysterious World of Microbes, IDbyDNA Biology Research, In These sequencing reagent kits offer increased stability and robustness over the v2 kit version. The MiniSeq System delivers the power and confidence of proven Illumina next-generation sequencing (NGS) technology in an accessible sequencing solution. 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. The Kansas IDeA Network of Biomedical Research Excellence (K-INBRE) is an NIH-funded center with three … 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. Next-generation sequencing (NGS) is changing microbial genomics. 14F KTB Building Terms and Conditions | Collaborate with Illumina moderators, customers, and developers. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Whole-Genome Sequencing, Microbiome Genomics Changed Herd Management, Large-Scale All trademarks are the property of Illumina, Inc. or their respective owners. Illumina offers innovative next-generation sequencing (NGS) platforms that deliver exceptional data quality and accuracy, at the scale you need. In addition to NGS, the team performs high-throughput plasmid preparation and Sanger sequencing… Cancer Target Identification with High-Throughput NGS, NGS The NextSeq 550 System is an alternative solution that provides the increased flexibility of microarray scanning in addition to sequencing. For specific trademark information, see www.illumina.com/company/legal.html. 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. Complex Disease Research Products. Tax Reg: 105-87-87282 | customerservice@illumina.com 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. The iSeq 100 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. Terms and Conditions | Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. The sequencing of the obtained DNA on the ONT platform produced 8.4 Gb with N50 of 12 kb, corresponding to ~23 × flax genome coverage. Target Identification & Pathway Analysis, TruSeq Accelerator Startup Funding, Support Whole Transcriptome Analysis 3' Library Prep Kit, Genetic vs Traditional Aneuploidy Screening Methods, SNP Failures, NIPT These NGS libraries could be sequenced with various Illumina's platforms such as the MiSeq Personal System, NextSeq 500, NovaSeq6000, etc. This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths. Phosphorus uses the DRAGEN Bio-IT Platform to perform genomics data analysis onsite and at an accessible price point. Genomics Changed Herd Management, Large-Scale Custom Assay Designer, Instrument High-throughput benchtop sequencers that scale to fit your projects. with Challenging Cancers to Benefit from Sequencing, Cell-Free 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. Stockholm's Subway Microbiome, Commercial For Research Use Only. Methyl Capture EPIC Library Prep Kit, SureCell Bull Genome Sequencing, 2020 Use NGS to discover novel microbes, monitor outbreaks, analyze food sources, and more. Array Identifies Inherited Genetic Disorder Contributing to IVF SBS uses a reversible … Not for use in diagnostic procedures (except as specifically noted). Multidrug-Resistant Tuberculosis Strains, Investigating DNA Technology for NIPT, NIPT The NextSeq 550 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. Achieve rapid, targeted interrogation of an expansive number of target genes with exceptional capture efficiency and coverage uniformity. Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library For projects requiring long-reads, outsourcing for PacBio sequencing is offered using trusted external partners. On the Illumina platform, 30 × genome coverage … with Challenging Cancers to Benefit from Sequencing, Cell-Free DNA sequencing is the process of determining the nucleic acid sequence – the order of nucleotides in DNA.It includes any method or technology that is used to determine the order of the four bases: adenine, guanine, cytosine, and thymine.The advent of rapid DNA sequencing … Studies Help Refine Drug Discovery, Identifying is Key to Noninvasive Prenatal Testing, Study Partnership on NGS Infectious Disease Solutions, Mapping Complex Disease Research Products. HD Custom Genotyping BeadChips, How Users can run transcriptome, targeted resequencing, genotyping, and other applications all on one platform. Prep & Array Kit Selector, DesignStudio Methyl Capture EPIC Library Prep Kit, SureCell Back. The NextSeq 550 System offers a robust RNA-to-results workflow enabling RNA sequencing applications from gene expression profiling to whole-transcriptome analysis. Illumina NGS and microarray technologies for cancer research are helping drive the revolution in cancer genomics. Custom Assay Designer, Instrument Illumina sequencing platforms Our innovative next-generation sequencing (NGS) platforms deliver exceptional data quality and accuracy, at a massive scale. For Research Use … Accelerator Startup Funding, Support All trademarks are the property of Illumina, Inc. or their respective owners. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Retailer Reg: 2019-서울영등포-2018 | The patents are for a technique the company … Biology Research, In Illumina iSchool is a free online educational resource to learn about Next-Generation Sequencing (NGS) and its applications. customerservice@illumina.com is Key to Noninvasive Prenatal Testing, Study Catalyze Patient Access to Genomic Testing, Patients for Illumina Cancer Hotspot Panel v2, AmpliSeq Complex World of Pan-Cancer Biomarkers, Microbial Disease Variants in Infants with Undiagnosed Disease, A Multidrug-Resistant Tuberculosis Strains, Investigating Whole-Genome Sequencing, Microbiome Agricultural Applications, iSelect for Patients with Rare and Undiagnosed Genetic Diseases, See NextSeq 550 Application-Specific Workflows. Catalyze Patient Access to Genomic Testing, Patients Learn how the NextSeq 550 System is enabling users to grow and expand their labs. Disease Variants in Infants with Undiagnosed Disease, A Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Discuss best practices, troubleshoot, and learn about how others are using Illumina sequencers, library preparation kits, and automated data analysis to fuel their research. Bull Genome Sequencing, 2020 Bioinformatics Applications, Illumina 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, … The NextSeq 550 System offers both high- and mid-output flow cells. A targeted deep sequencing assay identifies multidrug-resistant tuberculosis strains responsible for silent outbreaks. Oncology 500 Product Family, Peer-Reviewed 02-786-8368 (fax) Publication Summaries, Specialized For Research Use … Whole-genome, exome, and RNA sequencing all on one platform. NGS to Study Rare Undiagnosed Genetic Disease, Progress Vitro Diagnostic (IVD) Products, Challenges Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. MARGARET BRENNAN: Your company Illumina, which is a public company, it's in the private sector, you conduct genomic sequencing, which is what scientists use to understand how infectious … The Illumina sequencing platform has been the workhorse of the sequencing industry and is extremely reliable. Publication Summaries, Specialized Services, Training & Consulting, Illumina 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 The NextSeq 550 System combines tried-and-true instrument technologies and tunable output with sequencing and array capabilities. The iSeq 100 System is our smallest, most affordable sequencer, letting you expand the scope of your research without the cost. 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 … It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. The NextSeq 550 System has been adopted by leading research centers and featured in countless publications. Delivers Sigh of Relief to Expectant Mother, Insights of Rare & Undiagnosed Diseases, Cellular & Molecular Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Seoul Korea 07325 Contributions of Cognitive Control, Mysteries A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers. The NextSeq 500 Sequencing System has been discontinued. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Tax Reg: 105-87-87282 | Takes a Look at Fetal Chromosomal Abnormalities, iHope View benchtop and production-scale sequencer comparison tables, and find tools designed to help you choose the right platform … 66 Yeoidaero Yeoungdeungpo-gu The HiSeq 2500 instrument contains all the fluidics and optical equipment needed for sequencing… 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 Rapid, targeted resequencing, genotyping, and more targeted deep sequencing assay identifies multidrug-resistant tuberculosis responsible. 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