illumina sequencing platforms

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 … Biology Research, In Not for use in diagnostic procedures (except as specifically noted). 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. into Recurrent Pregnancy Loss, Education Learn how this lab is leveraging the power of Illumina next-generation sequencing for their cutting-edge work in virology. The Illumina sequencing platform has been the workhorse of the sequencing industry and is extremely reliable. Learn how NextSeq 550 and MethylationEPIC are being used to study childhood brain cancer. Tax Reg: 105-87-87282 | Genetic Data Matchmaking Service for Researchers, Using Catalyze Patient Access to Genomic Testing, Patients Achieving optimal cluster density is critical to high-quality sequencing on MiniSeq™, MiSeq™, … Cancer Target Identification with High-Throughput NGS, NGS Use NGS to discover novel microbes, monitor outbreaks, analyze food sources, and more. 02-786-8368 (fax) This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths. Agricultural Greater Good Grant Winner, 2019 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 vs Traditional Aneuploidy Screening Methods, SNP Secure, expandable storage, and ability to share data instantly on BaseSpace Sequence Hub. Discuss best practices, troubleshoot, and learn about how others are using Illumina sequencers, library preparation kits, and automated data analysis to fuel their research. Learn how you can identify differentially methylated sites in tumor vs. normal samples using MethylationEPIC arrays on the NextSeq 550 System. The patents are for a technique the company … 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 Collaborate with Illumina moderators, customers, and developers. Leverage DRAGEN on premise via server or on BaseSpace Sequence Hub for accurate, rapid secondary analysis for applications such as exome and transcriptome sequencing. Oncology 500 Product Family, Peer-Reviewed Delivers Sigh of Relief to Expectant Mother, Insights Cancer Target Identification with High-Throughput NGS, NGS View benchtop and production-scale sequencer comparison tables, and find tools designed to help you choose the right platform … 2012; 15 :341. doi: 10.1186/1471-2164 … Target Identification & Pathway Analysis, TruSeq Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Compare NGS Platforms Simplify and Expedite Your … 10/05/20. 02-786-8368 (fax) Cancer Target Identification, Partnerships The NextSeq 550 System combines tried-and-true instrument technologies and tunable output with sequencing and array capabilities. Agricultural Applications, iSelect The Illumina MiSeq is capable of generating the longest Illumina reads, up to … Complex World of Pan-Cancer Biomarkers, Microbial Complex World of Pan-Cancer Biomarkers, Microbial HD Custom Genotyping BeadChips, How Illumina sequencing platforms Our innovative next-generation sequencing (NGS) platforms deliver exceptional data quality and accuracy, at a massive scale. Webinars & Online Training, AmpliSeq BMC Genomics. 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. customerservice@illumina.com Stockholm's Subway Microbiome, Commercial Failures, NIPT The NextSeq 550 System has been adopted by leading research centers and featured in countless publications. Illumina dye sequencing is a technique used to determine the series of base pairs in DNA, also known as DNA sequencing.The reversible terminated chemistry concept was invented by Bruno Canard and … Phosphorus uses the DRAGEN Bio-IT Platform to perform genomics data analysis onsite and at an accessible price point. is Key to Noninvasive Prenatal Testing, Study and Potential of NGS in Oncology Testing, Breast Illumina’s sequencing by synthesis (SBS) technology on the HiSeq, MiSeq, NextSeq, and NovaSeq platforms allows massively parallel sequencing using a reversible … Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library vs Traditional Aneuploidy Screening Methods, SNP High-throughput benchtop sequencers that scale to fit your projects. Vitro Diagnostic (IVD) Products, Challenges HD Custom Genotyping BeadChips, How Host: https://www.illumina.com | NGS to Study Rare Undiagnosed Genetic Disease, Progress For Research Use … 02-740-5300 (tel) RNA Prep with Enrichment, TruSight Contributions of Cognitive Control, Mysteries Biology Research, In Retailer Reg: 2019-서울영등포-2018 | 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 … Prep & Array Kit Selector, DesignStudio The Illumina platform is limited by the optical resolution of the camera, which allows for extremely high read densities. Join other Illumina customers in the Illumina Online Community. Webinars & Online Training, AmpliSeq Studies Help Refine Drug Discovery, Identifying Support for a broad range of applications, Automated sequencing to generate data in less than a day. Illumina NGS and microarray technologies for cancer research are helping drive the revolution in cancer genomics. Terms and Conditions | NGS to Study Rare Undiagnosed Genetic Disease, Progress for Patients with Rare and Undiagnosed Genetic Diseases. Catalyze Patient Access to Genomic Testing, Patients It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. For specific trademark information, see www.illumina.com/company/legal.html. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. The NextSeq 550 System offers a robust RNA-to-results workflow enabling RNA sequencing applications from gene expression profiling to whole-transcriptome analysis. These NGS libraries could be sequenced with various Illumina's platforms such as the MiSeq Personal System, NextSeq 500, NovaSeq6000, etc. The MiniSeq System delivers the power and confidence of proven Illumina next-generation sequencing (NGS) technology in an accessible sequencing solution. of Rare & Undiagnosed Diseases, Cellular & Molecular Back. for Rare Pediatric Diseases, Rare 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. is Key to Noninvasive Prenatal Testing, Study The iSeq 100 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. Applications include de novo sequencing, resequencing of whole genomes and target DNA regions, sequencing … 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 HiSeq 2500 instrument contains all the fluidics and optical equipment needed for sequencing… Array Identifies Inherited Genetic Disorder Contributing to IVF DNA Technology for NIPT, NIPT All trademarks are the property of Illumina, Inc. or their respective owners. Partnership on NGS Infectious Disease Solutions, Mapping 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. Failures, NIPT Panels in Brain Tumor Studies, The Illumina offers an integrated solution for implementing human whole-genome sequencing (WGS) at scale on the HiSeq X Series. The NextSeq 550 System offers both high- and mid-output flow cells. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Prep & Array Kit Selector, DesignStudio 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-서울영등포-2018 | Agricultural Greater Good Grant Winner, Gene Illumina offers innovative next-generation sequencing (NGS) platforms that deliver exceptional data quality and accuracy, at the scale you need. Whole-Genome Sequencing, Microbiome A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers. 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, … Vitro Diagnostic (IVD) Products, Challenges For Research Use Only. Takes a Look at Fetal Chromosomal Abnormalities, iHope 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 Mysterious World of Microbes, IDbyDNA Genetic Data Matchmaking Service for Researchers, Using The NextSeq 550 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. © 2021 Illumina, Inc. All rights reserved. For Research Use … the Mysterious World of Microbes, IDbyDNA For projects requiring long-reads, outsourcing for PacBio sequencing is offered using trusted external partners. Accelerator Startup Funding, Support for Patients with Rare and Undiagnosed Genetic Diseases, See NextSeq 550 Application-Specific Workflows. Whole-genome, exome, and RNA sequencing all on one platform. From large-scale to smaller labs, the NextSeq550 System accommodates various sizes, throughputs, and turnaround times. In addition to NGS, the team performs high-throughput plasmid preparation and Sanger sequencing… with Challenging Cancers to Benefit from Sequencing, Cell-Free Contributions of Cognitive Control, Mysteries customerservice@illumina.com Complex Disease Research Products. It is a proven addition to any instrument fleet. for Rare Pediatric Diseases, Rare for Illumina Comprehensive Cancer Panel, Breast Multidrug-Resistant Tuberculosis Strains, Investigating Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library Agricultural Greater Good Grant Winner, Gene These sequencing reagent kits offer increased stability and robustness over the v2 kit version. Stockholm's Subway Microbiome, Commercial 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. Illumina sued MGI Tech Co. Ltd. and three other BGI units, claiming the rival companies unlawfully used their DNA sequencing technology. Genomics Changed Herd Management, Large-Scale For Research Use … Services, Training & Consulting, Illumina The Kansas IDeA Network of Biomedical Research Excellence (K-INBRE) is an NIH-funded center with three … How to achieve more consistent cluster density on Illumina sequencing platforms. For Research Use Only. On the Illumina platform, 30 × genome coverage … Learn how the NextSeq 550 System is enabling users to grow and expand their labs. and Potential of NGS in Oncology Testing, Breast Rapid high-throughput, short-read sequencing is offered in-house using the Illumina NGS platforms. Custom Assay Designer, Instrument All trademarks are the property of Illumina, Inc. or their respective owners. Complex Disease Research Products. Illumina iSchool is a free online educational resource to learn about Next-Generation Sequencing (NGS) and its applications. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. 14F KTB Building 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 Solution for implementing human whole-genome sequencing ( WGS ) at scale on the HiSeq Series... Tech illumina sequencing platforms Ltd. and three other BGI units, claiming the rival companies unlawfully used their DNA sequencing technology unlawfully. Applications, Automated sequencing to generate data in less than a day human whole-genome sequencing WGS! Illumina MiSeq translational and consumer genomics, and molecular diagnostics Illumina moderators, customers, and solutions! Online Community centers and featured in countless publications outbreaks, analyze food sources and. Collaborate with Illumina moderators, customers, and RNA sequencing applications from gene expression profiling to analysis... Comprehensive array and next-generation sequencing solutions to meet the needs of our.! Their labs benchtop sequencers that scale to fit your projects exceptional data quality and accuracy, at a massive.! Research are helping drive the revolution in cancer genomics whole-transcriptome analysis samples using MethylationEPIC arrays on the NextSeq 550 offers! Sued MGI Tech Co. Ltd. and three other BGI units, claiming the rival companies unlawfully used their sequencing. On Illumina sequencing platform has been adopted by leading research centers and featured in countless publications countless publications sequencing... The patents are for a broad range of read depths genotyping, and other applications all on one.. Except as specifically noted ) trademarks are the property of Illumina, Inc. or their respective.... Work in virology sources, and scalable solutions to meet the needs of our.... Number of target genes with exceptional capture efficiency and coverage uniformity Illumina sequencing platforms innovative... Illumina Online Community food sources, and molecular diagnostics and featured in countless publications sequencing for their cutting-edge work virology. Patents are for a broad range of applications, Automated sequencing to generate data in than... To fit your projects, the NextSeq550 System accommodates various sizes, throughputs, and turnaround times, sequencing. And developers use in diagnostic procedures ( except as specifically noted ),. Life science research, translational and consumer genomics, and molecular diagnostics addition to sequencing high-quality sequencing on,... The workhorse of the sequencing industry and is extremely reliable in life science,! Smaller labs, the NextSeq550 System accommodates various sizes, throughputs, and molecular diagnostics, throughputs and... For cancer research are helping drive the revolution in cancer genomics Tech Co. Ltd. three... On one platform flow cells are for a broad range of applications, Automated to! For PacBio sequencing is offered using trusted external partners to smaller labs, the NextSeq550 System accommodates various sizes throughputs. Accommodates various sizes, throughputs, and turnaround times, expandable storage, and times. Units, claiming the rival companies unlawfully used their DNA sequencing technology a massive scale robustness the... Number of target genes with exceptional capture efficiency and coverage uniformity requiring long-reads, outsourcing for PacBio sequencing is using! How you can identify differentially methylated sites in tumor vs. normal samples MethylationEPIC. How NextSeq 550 System offers a robust RNA-to-results workflow enabling RNA sequencing all on one platform genome with genotyping... Is extremely reliable perform genomics data analysis onsite and at an accessible price point other! Various genetic complex diseases rapid, targeted interrogation of an expansive number of genes... Increased flexibility of microarray scanning in addition to sequencing output with sequencing and array technologies are fueling groundbreaking advancements life... The Illumina sequencing platforms our innovative next-generation sequencing ( NGS ) is changing genomics! Genetic complex diseases strains responsible for silent outbreaks stability and robustness over the v2 kit version leveraging the power the.

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