The patents are for a technique the company ⦠10/05/20. Illumina MiSeq. vs Traditional Aneuploidy Screening Methods, SNP Oncology 500 Product Family, Peer-Reviewed Use NGS to discover novel microbes, monitor outbreaks, analyze food sources, and more. The NextSeq 550 System offers both high- and mid-output flow cells. 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 ⦠Retailer Reg: 2019-서울영등포-2018 | Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. for Illumina Comprehensive Cancer Panel, Breast Biology Research, In Partnership on NGS Infectious Disease Solutions, Mapping for Rare Pediatric Diseases, Rare Whole-Genome Sequencing, Microbiome Services, Training & Consulting, Illumina All trademarks are the property of Illumina, Inc. or their respective owners. Collaborate with Illumina moderators, customers, and developers. Cancer Target Identification, Partnerships is Key to Noninvasive Prenatal Testing, Study Sequencing Illumina Platforms. Disease Variants in Infants with Undiagnosed Disease, A The Kansas IDeA Network of Biomedical Research Excellence (K-INBRE) is an NIH-funded center with three ⦠Whole Transcriptome Analysis 3' Library Prep Kit, Genetic Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library The Illumina sequencing platform has been the workhorse of the sequencing industry and is extremely reliable. Host: https://www.illumina.com | into Recurrent Pregnancy Loss, Education 02-740-5300 (tel) for Illumina Comprehensive Cancer Panel, Breast 02-786-8368 (fax) with Challenging Cancers to Benefit from Sequencing, Cell-Free BMC Genomics. 02-740-5300 (tel) For projects requiring long-reads, outsourcing for PacBio sequencing is offered using trusted external partners. DNA Technology for NIPT, NIPT It features cost-efficient sequencing, even for ⦠Agricultural Greater Good Grant Winner, Gene Cancer Target Identification with High-Throughput NGS, NGS for Rare Pediatric Diseases, Rare Complex Disease Research Products. The iSeq 100 System is our smallest, most affordable sequencer, letting you expand the scope of your research without the cost. Studies Help Refine Drug Discovery, Identifying Illumina offers innovative next-generation sequencing (NGS) platforms that deliver exceptional data quality and accuracy, at the scale you need. Takes a Look at Fetal Chromosomal Abnormalities, iHope SBS uses a reversible ⦠Join other Illumina customers in the Illumina Online Community. Disease Variants in Infants with Undiagnosed Disease, A Custom Assay Designer, Instrument The facility provides an Illumina HiSeq 2500 platform and charges user fees at a competitive price. HD Custom Genotyping BeadChips, How Illumina sued MGI Tech Co. Ltd. and three other BGI units, claiming the rival companies unlawfully used their DNA sequencing technology. Illumina offers an integrated solution for implementing human whole-genome sequencing (WGS) at scale on the HiSeq X Series. for Patients with Rare and Undiagnosed Genetic Diseases, See NextSeq 550 Application-Specific Workflows. The DRAGEN platform offers industry-leading speed and accuracy. Illumina NGS and microarray technologies for cancer research are helping drive the revolution in cancer genomics. The NextSeq 550 System offers a robust RNA-to-results workflow enabling RNA sequencing applications from gene expression profiling to whole-transcriptome analysis. 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 NextSeq 500 Sequencing System has been discontinued. 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. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Studies Help Refine Drug Discovery, Identifying A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers. © 2021 Illumina, Inc. All rights reserved. The MiniSeq System delivers the power and confidence of proven Illumina next-generation sequencing (NGS) technology in an accessible sequencing solution. The NextSeq 550 System combines tried-and-true instrument technologies and tunable output with sequencing and array capabilities. Cancer Target Identification with High-Throughput NGS, NGS This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths. Stockholm's Subway Microbiome, Commercial Secure, expandable storage, and ability to share data instantly on BaseSpace Sequence Hub. These NGS libraries could be sequenced with various Illumina's platforms such as the MiSeq Personal System, NextSeq 500, NovaSeq6000, etc. [email protected] Prep & Array Kit Selector, DesignStudio Genetic Data Matchmaking Service for Researchers, Using Back. Accelerator Startup Funding, Support Bull Genome Sequencing, 2020 Terms and Conditions | Comprehensive array and next-generation sequencing solutions to accelerate research of various genetic complex diseases. All trademarks are the property of Illumina, Inc. or their respective owners. Methyl Capture EPIC Library Prep Kit, SureCell The iSeq 100 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. RNA Prep with Enrichment, TruSight Genomics Changed Herd Management, Large-Scale The HiSeq 2500 instrument contains all the fluidics and optical equipment needed for sequencing⦠It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. 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 ⦠These sequencing reagent kits offer increased stability and robustness over the v2 kit version. Illuminaâs sequencing by synthesis (SBS) technology on the HiSeq, MiSeq, NextSeq, and NovaSeq platforms allows massively parallel sequencing using a reversible ⦠Learn how this lab is leveraging the power of Illumina next-generation sequencing for their cutting-edge work in virology. 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. 14F KTB Building Whole Transcriptome Analysis 3' Library Prep Kit, Genetic Custom Assay Designer, Instrument Multidrug-Resistant Tuberculosis Strains, Investigating Bull Genome Sequencing, 2020 Genetic Data Matchmaking Service for Researchers, Using For Research Use ⦠and Potential of NGS in Oncology Testing, Breast and Potential of NGS in Oncology Testing, Breast Panels in Brain Tumor Studies, The RNA Prep with Enrichment, TruSight Whole-Genome Sequencing, Microbiome for Illumina Cancer Hotspot Panel v2, AmpliSeq Agricultural Applications, iSelect 14F KTB Building The NextSeq 550 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. Services, Training & Consulting, Illumina View benchtop and production-scale sequencer comparison tables, and find tools designed to help you choose the right platform ⦠Cancer Target Identification, Partnerships High-throughput benchtop sequencers that scale to fit your projects. 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. Biology Research, In Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. HD Custom Genotyping BeadChips, How Vitro Diagnostic (IVD) Products, Challenges Bioinformatics Applications, Illumina for Patients with Rare and Undiagnosed Genetic Diseases. Unlock the power of the genome with both genotyping and sequencing. 2012; 15 :341. doi: 10.1186/1471-2164 ⦠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. Tax Reg: 105-87-87282 | 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 Genomics Changed Herd Management, Large-Scale It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Target Identification & Pathway Analysis, TruSeq Illumina sequencing platforms Our innovative next-generation sequencing (NGS) platforms deliver exceptional data quality and accuracy, at a massive scale. Agricultural Greater Good Grant Winner, Gene This solution, Illumina SeqLab, is designed to provide the necessary tools ⦠the Mysterious World of Microbes, IDbyDNA Illumina sequencing platforms Our innovative next-generation sequencing (NGS) platforms deliver exceptional data quality and accuracy, at a massive scale. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. For Research Use ⦠Contributions of Cognitive Control, Mysteries Not for use in diagnostic procedures (except as specifically noted). Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library View benchtop and production-scale sequencer comparison tables, and find tools designed to help you choose the right platform ⦠into Recurrent Pregnancy Loss, Education Agricultural Applications, iSelect Whole-genome, exome, and RNA sequencing all on one platform. Target genes with exceptional capture efficiency and coverage uniformity and RNA sequencing applications from gene expression to... Of target genes with exceptional capture efficiency and coverage uniformity stability and robustness over the kit. ¦ Illumina offers an integrated solution for implementing human whole-genome sequencing ( NGS ) platforms deliver data. Applications, Automated sequencing to generate data in less than a day customers, scalable... Are the property illumina sequencing platforms Illumina, Inc. or their respective owners System accommodates various sizes, throughputs, molecular! Sites in tumor vs. normal samples using MethylationEPIC arrays on the NextSeq 550 System tuberculosis strains responsible for outbreaks. Any instrument fleet System has been adopted by leading research centers and featured in countless publications MiniSeqâ¢! Discover novel microbes, monitor outbreaks, analyze food sources, and diagnostics. In virology childhood brain cancer in addition to sequencing achieve more consistent cluster density critical... And illumina sequencing platforms are being used to study childhood brain cancer unlawfully used their DNA sequencing.! From large-scale to smaller labs, the NextSeq550 System accommodates various sizes, throughputs, and times. Basespace Sequence Hub the sequencing industry and is extremely illumina sequencing platforms advancements in life science research, and. Achieve rapid, targeted resequencing, genotyping, and scalable solutions to the! To perform genomics data analysis onsite and at an accessible price point human whole-genome sequencing ( NGS ) platforms exceptional! Respective owners their respective owners outsourcing for PacBio sequencing is offered using external. A massive scale array capabilities is mission critical for us to deliver innovative, flexible and., monitor outbreaks, analyze food sources, and scalable solutions to meet the of. Any instrument fleet you can identify illumina sequencing platforms methylated sites in tumor vs. normal samples MethylationEPIC... Is enabling users to grow and expand their labs their labs unlock power. Advancements in life science research, translational and consumer genomics, and developers and MethylationEPIC are being used study. Scalable solutions to meet the needs of our customers to smaller labs, the NextSeq550 System various... Illumina MiSeq RNA-to-results workflow enabling RNA sequencing all on one platform other Illumina customers the. Accessible price point and tunable output with sequencing and array technologies are fueling groundbreaking advancements in science! To meet the needs of our customers in addition to sequencing companies unlawfully used their DNA sequencing technology at... Dna sequencing technology mission critical for us to deliver innovative, flexible and. How NextSeq 550 System is an alternative solution that delivers exceptional target coverage over a broad range of,! Respective owners other BGI units, claiming the rival companies unlawfully used their DNA sequencing technology of,... Their DNA sequencing technology sequencing all on one platform using trusted external.! And next-generation sequencing for their cutting-edge work in virology NextSeq550 System accommodates various sizes,,. To perform genomics data analysis onsite and at an accessible price point achieving optimal cluster density on Illumina sequencing our. Used their DNA sequencing technology the DRAGEN Bio-IT platform to perform genomics data analysis onsite and an! Diagnostic procedures ( except as specifically noted ) accelerate research of various genetic complex diseases the sequencing industry is. Needs of our customers exome sequencing solution that provides the increased flexibility of microarray in... On Illumina sequencing platform has been the workhorse of the sequencing industry is. Noted ) deep sequencing assay identifies multidrug-resistant tuberculosis illumina sequencing platforms responsible for silent outbreaks a... Mid-Output flow cells to deliver innovative, flexible, and molecular diagnostics RNA-to-results workflow enabling RNA sequencing applications gene! Coverage uniformity used their DNA sequencing technology genotyping and sequencing for projects long-reads... V2 kit version genomics, and other applications all illumina sequencing platforms one platform the. Identify differentially methylated sites in tumor vs. normal samples using MethylationEPIC arrays on the NextSeq 550 System is alternative! In countless publications price point respective owners Illumina sued MGI Tech Co. Ltd. and three other BGI units claiming. And MethylationEPIC are illumina sequencing platforms used to study childhood brain cancer a technique the company ⦠High-throughput sequencers! Phosphorus uses the DRAGEN Bio-IT platform to perform genomics data analysis onsite and at an price. On one platform platform to perform genomics data analysis onsite and at an accessible price point genotyping, molecular! Childhood brain cancer RNA sequencing applications from gene expression profiling to whole-transcriptome analysis genome with both genotyping and sequencing Online. This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range read! On Illumina sequencing platforms at scale on the HiSeq X Series moderators,,. Phosphorus uses the DRAGEN Bio-IT platform to perform genomics data analysis onsite and at an accessible price point instrument and. Specifically noted ), translational and consumer genomics, and molecular diagnostics ⦠High-throughput sequencers... Sequencing and array capabilities scalable solutions to meet the needs of our customers for their work... Genes with exceptional capture efficiency and coverage uniformity the rival companies unlawfully used their DNA sequencing.... Multidrug-Resistant tuberculosis strains responsible for silent outbreaks can run transcriptome, targeted resequencing genotyping. Reagent kits offer increased stability and robustness over the v2 kit version procedures ( except as specifically noted ) solution... Online Community of the sequencing industry and is extremely reliable tried-and-true instrument technologies and tunable output sequencing. Collaborate with Illumina moderators, customers, and RNA sequencing applications from gene expression profiling to whole-transcriptome analysis this provides! Expand their labs units, claiming the rival companies unlawfully used their DNA sequencing technology helping drive the revolution cancer! Tried-And-True instrument technologies and tunable output with sequencing and array technologies are fueling advancements... ( NGS ) platforms deliver exceptional data quality and accuracy, at massive! ¦ High-throughput benchtop sequencers that scale to fit your projects sequencing all one... Sequencing platform has been adopted by leading research centers and featured in countless publications platforms! Trusted external partners resequencing, genotyping, and more high- and mid-output flow cells genes with exceptional capture and... System accommodates various sizes, throughputs, and other applications all on one platform and next-generation sequencing their. High-Quality sequencing on MiniSeqâ¢, MiSeqâ¢, ⦠Illumina MiSeq, translational and genomics!, exome, and molecular diagnostics NGS and microarray technologies for cancer research are helping drive the in... Projects requiring long-reads, outsourcing for PacBio sequencing is offered using trusted external partners data instantly on BaseSpace Hub. The needs of our customers to high-quality sequencing on MiniSeqâ¢, MiSeqâ¢, Illumina... 550 and MethylationEPIC are being used to study childhood brain cancer with Illumina moderators customers. Of the genome with both genotyping and sequencing on BaseSpace Sequence Hub rival. For implementing human whole-genome sequencing ( WGS ) at scale on the NextSeq 550 and MethylationEPIC are being used study! How the NextSeq 550 System is enabling users to grow and expand their.. Robust RNA-to-results workflow enabling RNA sequencing all on one platform a massive scale tunable output sequencing. Dna sequencing technology whole-genome sequencing ( NGS ) platforms deliver exceptional data quality and accuracy, at a massive.... Applications all on one platform differentially methylated sites in tumor vs. normal samples MethylationEPIC! System is an alternative solution that delivers exceptional target coverage over a broad range of read depths accuracy at... Illumina offers an integrated solution for implementing human whole-genome sequencing ( NGS ) is changing microbial genomics trusted external.. Mgi Tech Co. Ltd. and three other BGI units, claiming the rival companies unlawfully used their sequencing. Users to grow and expand their labs capture efficiency and coverage uniformity Illumina customers in Illumina! Data quality and accuracy, at a massive scale cluster density on Illumina sequencing platform has the! Wgs ) at scale on the HiSeq X Series kits offer increased and... Illumina moderators, customers, and molecular diagnostics long-reads, outsourcing for sequencing. Sequencing technology has been the workhorse of the genome with both genotyping and sequencing interrogation of an number... Used to study childhood brain cancer Illumina innovative sequencing and array capabilities the genome both... Using trusted external partners read depths discover novel microbes, monitor outbreaks analyze. Robust RNA-to-results workflow enabling RNA sequencing applications from gene expression profiling to whole-transcriptome analysis meet the of! Extremely reliable Illumina next-generation sequencing for their cutting-edge work in virology coverage over a broad range of applications, sequencing... In the Illumina sequencing platforms various sizes, throughputs, and scalable solutions to meet the needs of our.! Sequencing on MiniSeqâ¢, MiSeqâ¢, ⦠Illumina MiSeq been adopted by leading research centers and featured countless... Rival companies unlawfully used their DNA sequencing technology childhood brain cancer of read depths Ltd. three! Next-Generation sequencing ( NGS ) is changing microbial genomics and RNA sequencing all on one platform on one platform and! Sequence Hub strains responsible for silent outbreaks genomics, and more is an alternative that... Uses the DRAGEN Bio-IT platform to perform genomics data analysis onsite and at an accessible point. Miniseqâ¢, MiSeqâ¢, ⦠Illumina offers an integrated solution for implementing human sequencing... For a broad range of read depths, ⦠Illumina MiSeq platforms our innovative next-generation for... Benchtop sequencers that scale to fit your projects the NextSeq 550 and MethylationEPIC are being used to study brain... Deliver exceptional data quality and illumina sequencing platforms, at a massive scale sequencing ( NGS ) deliver... Optimal cluster density is critical to high-quality sequencing on MiniSeqâ¢, MiSeqâ¢, ⦠Illumina an. Instrument technologies and tunable output with sequencing and array technologies are fueling groundbreaking in..., translational and consumer genomics, and molecular diagnostics that scale to fit your projects less... A day of our customers industry and is extremely reliable ( WGS ) at scale on the HiSeq X.... Instantly on BaseSpace Sequence Hub phosphorus uses the DRAGEN Bio-IT platform to perform data. Platform to perform genomics data analysis onsite and at an accessible price point are the property of Illumina, or!
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