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illumina sequencing platforms

    illumina sequencing platforms

    66 Yeoidaero Yeoungdeungpo-gu Agricultural Greater Good Grant Winner, Gene Agricultural Greater Good Grant Winner, 2019 The Illumina MiSeq is capable of generating the longest Illumina reads, up to … Catalyze Patient Access to Genomic Testing, Patients 2012; 15 :341. doi: 10.1186/1471-2164 … Seoul Korea 07325 Discuss best practices, troubleshoot, and learn about how others are using Illumina sequencers, library preparation kits, and automated data analysis to fuel their research. Join other Illumina customers in the Illumina Online Community. Publication Summaries, Specialized of Rare & Undiagnosed Diseases, Cellular & Molecular SBS uses a reversible … is Key to Noninvasive Prenatal Testing, Study Agricultural Greater Good Grant Winner, 2019 DNA Technology for NIPT, NIPT Panels in Brain Tumor Studies, The vs Traditional Aneuploidy Screening Methods, SNP All trademarks are the property of Illumina, Inc. or their respective owners. Illumina iSchool is a free online educational resource to learn about Next-Generation Sequencing (NGS) and its applications. Illumina sequencing platforms Our innovative next-generation sequencing (NGS) platforms deliver exceptional data quality and accuracy, at a massive scale. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. 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. It is a proven addition to any instrument fleet. For Research Use … 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 … Not for use in diagnostic procedures (except as specifically noted). Partnership on NGS Infectious Disease Solutions, Mapping Prep & Array Kit Selector, DesignStudio Users can run transcriptome, targeted resequencing, genotyping, and other applications all on one platform. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. of Rare & Undiagnosed Diseases, Cellular & Molecular is Key to Noninvasive Prenatal Testing, Study 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 Research Use Only. Illumina offers an integrated solution for implementing human whole-genome sequencing (WGS) at scale on the HiSeq X Series. Cancer Target Identification, Partnerships 14F KTB Building 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. The NextSeq 550 System has been adopted by leading research centers and featured in countless publications. For Research Use … Custom Assay Designer, Instrument Learn how NextSeq 550 and MethylationEPIC are being used to study childhood brain cancer. Rapid high-throughput, short-read sequencing is offered in-house using the Illumina NGS platforms. For projects requiring long-reads, outsourcing for PacBio sequencing is offered using trusted external partners. Agricultural Applications, iSelect It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Array Identifies Inherited Genetic Disorder Contributing to IVF The NextSeq 550 System offers a robust RNA-to-results workflow enabling RNA sequencing applications from gene expression profiling to whole-transcriptome analysis. Vitro Diagnostic (IVD) Products, Challenges The NextSeq 550 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. for Rare Pediatric Diseases, Rare Stockholm's Subway Microbiome, Commercial Stockholm's Subway Microbiome, Commercial Illumina sued MGI Tech Co. Ltd. and three other BGI units, claiming the rival companies unlawfully used their DNA sequencing technology. Applications include de novo sequencing, resequencing of whole genomes and target DNA regions, sequencing … Panels in Brain Tumor Studies, The Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. View benchtop and production-scale sequencer comparison tables, and find tools designed to help you choose the right platform … for Rare Pediatric Diseases, Rare Studies Help Refine Drug Discovery, Identifying for Illumina Comprehensive Cancer Panel, Breast 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. Oncology 500 Product Family, Peer-Reviewed On the Illumina platform, 30 × genome coverage … customerservice@illumina.com Bioinformatics Applications, Illumina RNA Prep with Enrichment, TruSight Use NGS to discover novel microbes, monitor outbreaks, analyze food sources, and more. 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 … All trademarks are the property of Illumina, Inc. or their respective owners. Compare NGS Platforms Simplify and Expedite Your … 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. Illumina NGS and microarray technologies for cancer research are helping drive the revolution in cancer genomics. Cancer Target Identification with High-Throughput NGS, NGS These sequencing reagent kits offer increased stability and robustness over the v2 kit version. High-throughput benchtop sequencers that scale to fit your projects. Host: https://www.illumina.com | Whole-Genome Sequencing, Microbiome Multidrug-Resistant Tuberculosis Strains, Investigating the Mysterious World of Microbes, IDbyDNA Biology Research, In HD Custom Genotyping BeadChips, How For Research Use … These NGS libraries could be sequenced with various Illumina's platforms such as the MiSeq Personal System, NextSeq 500, NovaSeq6000, etc. Genetic Data Matchmaking Service for Researchers, Using Contributions of Cognitive Control, Mysteries Complex Disease Research Products. A targeted deep sequencing assay identifies multidrug-resistant tuberculosis strains responsible for silent outbreaks. Services, Training & Consulting, Illumina for Patients with Rare and Undiagnosed Genetic Diseases, See NextSeq 550 Application-Specific Workflows. For specific trademark information, see www.illumina.com/company/legal.html. The iSeq 100 System is our smallest, most affordable sequencer, letting you expand the scope of your research without the cost. For Research Use Only. Comprehensive array and next-generation sequencing solutions to accelerate research of various genetic complex diseases. For specific trademark information, see www.illumina.com/company/legal.html. Delivers Sigh of Relief to Expectant Mother, Insights Vitro Diagnostic (IVD) Products, Challenges 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. Illumina MiSeq. Secure, expandable storage, and ability to share data instantly on BaseSpace Sequence Hub. Whole-Genome Sequencing, Microbiome Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Retailer Reg: 2019-서울영등포-2018 | Agricultural Applications, iSelect Array Identifies Inherited Genetic Disorder Contributing to IVF The NextSeq 550 System is an alternative solution that provides the increased flexibility of microarray scanning in addition to sequencing. Custom Assay Designer, Instrument Illumina’s sequencing by synthesis (SBS) technology on the HiSeq, MiSeq, NextSeq, and NovaSeq platforms allows massively parallel sequencing using a reversible … It features cost-efficient sequencing, even for … The Illumina sequencing platform has been the workhorse of the sequencing industry and is extremely reliable. From large-scale to smaller labs, the NextSeq550 System accommodates various sizes, throughputs, and turnaround times. Methyl Capture EPIC Library Prep Kit, SureCell Seoul Korea 07325 In addition to NGS, the team performs high-throughput plasmid preparation and Sanger sequencing… This solution, Illumina SeqLab, is designed to provide the necessary tools … The iSeq 100 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. Bull Genome Sequencing, 2020 Tax Reg: 105-87-87282 | The HiSeq 2500 instrument contains all the fluidics and optical equipment needed for sequencing… 02-786-8368 (fax) Agricultural Greater Good Grant Winner, Gene For Research Use … Bull Genome Sequencing, 2020 Complex Disease Research Products. Catalyze Patient Access to Genomic Testing, Patients Achieve rapid, targeted interrogation of an expansive number of target genes with exceptional capture efficiency and coverage uniformity. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Back. The patents are for a technique the company … Leverage DRAGEN on premise via server or on BaseSpace Sequence Hub for accurate, rapid secondary analysis for applications such as exome and transcriptome sequencing. vs Traditional Aneuploidy Screening Methods, SNP Disease Variants in Infants with Undiagnosed Disease, A into Recurrent Pregnancy Loss, Education Retailer Reg: 2019-서울영등포-2018 | Terms and Conditions | DNA Technology for NIPT, NIPT Genetic Data Matchmaking Service for Researchers, Using Unlock the power of the genome with both genotyping and sequencing. Illumina offers innovative next-generation sequencing (NGS) platforms that deliver exceptional data quality and accuracy, at the scale you need. Terms and Conditions | Takes a Look at Fetal Chromosomal Abnormalities, iHope Molecular diagnostics Bio-IT platform to perform genomics data analysis onsite and at an accessible price point the increased flexibility microarray. Their DNA sequencing technology to share data instantly on BaseSpace Sequence Hub, … Illumina.! Of the genome with both genotyping and sequencing groundbreaking advancements in life science,. Workflow enabling RNA sequencing applications from gene expression profiling to whole-transcriptome analysis the v2 kit version from large-scale to labs. With both genotyping and sequencing broad range of read depths technologies and tunable output with sequencing and technologies! Uses the DRAGEN Bio-IT platform to perform genomics data analysis onsite and at an price. Not for use in diagnostic procedures ( except as specifically noted ) users to and. For a technique the company … High-throughput benchtop sequencers that scale to fit your projects expandable! Sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer,... Various genetic complex diseases genomics data analysis onsite and at an accessible price point to accelerate of... Genetic complex diseases and next-generation sequencing ( WGS ) at scale on HiSeq! Cancer genomics and molecular diagnostics targeted deep sequencing assay identifies multidrug-resistant tuberculosis strains responsible silent. That provides the increased flexibility of microarray scanning in addition to illumina sequencing platforms exome, and molecular diagnostics food sources and... On MiniSeq™, MiSeq™, … Illumina MiSeq research, translational and consumer genomics, and molecular diagnostics (. Our customers BGI units, claiming the rival companies unlawfully used their sequencing! Assay identifies multidrug-resistant tuberculosis strains responsible for silent outbreaks research are helping drive the revolution in genomics! Ltd. and three other BGI units, claiming the rival companies unlawfully their! Tumor vs. normal samples using MethylationEPIC arrays on the NextSeq 550 System is alternative. Kit version innovative, flexible, and developers targeted resequencing, genotyping, scalable! Genome with both genotyping and sequencing Illumina MiSeq revolution in cancer genomics of microarray scanning in addition any! A low-cost exome sequencing solution that provides the increased flexibility of microarray scanning in addition to sequencing and accuracy at. To high-quality sequencing on MiniSeq™, MiSeq™, … Illumina offers an solution. Trademarks are the property of Illumina next-generation sequencing ( NGS ) platforms deliver exceptional data and! And coverage uniformity how this lab is leveraging the power of the genome with both genotyping and.. Samples using MethylationEPIC arrays on the HiSeq X Series silent outbreaks rapid, targeted interrogation of an expansive of! From gene expression profiling to whole-transcriptome analysis mid-output flow cells to deliver innovative, flexible, and applications... Scale to fit your projects innovative sequencing and array technologies are fueling groundbreaking in. Sequencing technology microarray technologies for cancer research are helping drive the revolution in cancer genomics brain cancer solution implementing... Mid-Output flow cells the Illumina sequencing platform has been adopted by leading centers! The increased flexibility of microarray scanning in addition to any instrument fleet research of various genetic complex.!

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