Cancer Target Identification, Partnerships Whole-genome, exome, and RNA sequencing all on one platform. For Research Use Only. Leverage DRAGEN on premise via server or on BaseSpace Sequence Hub for accurate, rapid secondary analysis for applications such as exome and transcriptome sequencing. 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. Tax Reg: 105-87-87282 | Collaborate with Illumina moderators, customers, and developers. Agricultural Applications, iSelect Accelerator Startup Funding, Support Catalyze Patient Access to Genomic Testing, Patients All trademarks are the property of Illumina, Inc. or their respective owners. Accelerator Startup Funding, Support 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 … For specific trademark information, see www.illumina.com/company/legal.html. 14F KTB Building Next-generation sequencing (NGS) is changing microbial genomics. Unlock the power of the genome with both genotyping and sequencing. Seoul Korea 07325 The patents are for a technique the company … Multidrug-Resistant Tuberculosis Strains, Investigating for Illumina Cancer Hotspot Panel v2, AmpliSeq Applications include de novo sequencing, resequencing of whole genomes and target DNA regions, sequencing … 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. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Rapid high-throughput, short-read sequencing is offered in-house using the Illumina NGS platforms. Prep & Array Kit Selector, DesignStudio All trademarks are the property of Illumina, Inc. or their respective owners. The Illumina sequencing platform has been the workhorse of the sequencing industry and is extremely reliable. HD Custom Genotyping BeadChips, How High-throughput benchtop sequencers that scale to fit your projects. On the Illumina platform, 30 × genome coverage … RNA Prep with Enrichment, TruSight Genomics Changed Herd Management, Large-Scale Oncology 500 Product Family, Peer-Reviewed The NextSeq 550 System is an alternative solution that provides the increased flexibility of microarray scanning in addition to sequencing. How to achieve more consistent cluster density on Illumina sequencing platforms. Oncology 500 Product Family, Peer-Reviewed Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Learn how this lab is leveraging the power of Illumina next-generation sequencing for their cutting-edge work in virology. Whole Transcriptome Analysis 3' Library Prep Kit, Genetic 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. Complex Disease Research Products. NGS to Study Rare Undiagnosed Genetic Disease, Progress 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 Seoul Korea 07325 Cancer Target Identification, Partnerships A targeted deep sequencing assay identifies multidrug-resistant tuberculosis strains responsible for silent outbreaks. the Mysterious World of Microbes, IDbyDNA SBS uses a reversible … The iSeq 100 System harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. Methyl Capture EPIC Library Prep Kit, SureCell Delivers Sigh of Relief to Expectant Mother, Insights For Research Use … Back. Partnership on NGS Infectious Disease Solutions, Mapping SBS uses a reversible … These NGS libraries could be sequenced with various Illumina's platforms such as the MiSeq Personal System, NextSeq 500, NovaSeq6000, etc. Sequencing Illumina Platforms. Delivers Sigh of Relief to Expectant Mother, Insights Not for use in diagnostic procedures (except as specifically noted). Complex World of Pan-Cancer Biomarkers, Microbial Illumina sued MGI Tech Co. Ltd. and three other BGI units, claiming the rival companies unlawfully used their DNA sequencing technology. with Challenging Cancers to Benefit from Sequencing, Cell-Free View benchtop and production-scale sequencer comparison tables, and find tools designed to help you choose the right platform … Illumina offers an integrated solution for implementing human whole-genome sequencing (WGS) at scale on the HiSeq X Series. RNA Prep with Enrichment, TruSight Webinars & Online Training, AmpliSeq Achieve rapid, targeted interrogation of an expansive number of target genes with exceptional capture efficiency and coverage uniformity. These sequencing reagent kits offer increased stability and robustness over the v2 kit version. Failures, NIPT Join other Illumina customers in the Illumina Online Community. The MiniSeq System delivers the power and confidence of proven Illumina next-generation sequencing (NGS) technology in an accessible sequencing solution. 02-786-8368 (fax) Biology Research, In From large-scale to smaller labs, the NextSeq550 System accommodates various sizes, throughputs, and turnaround times. 02-786-8368 (fax) is Key to Noninvasive Prenatal Testing, Study 2012; 15 :341. doi: 10.1186/1471-2164 … Biology Research, In Bull Genome Sequencing, 2020 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. Users can run transcriptome, targeted resequencing, genotyping, and other applications all on one platform. Illumina’s sequencing by synthesis (SBS) technology on the HiSeq, MiSeq, NextSeq, and NovaSeq platforms allows massively parallel sequencing using a reversible … A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers. Complex Disease Research Products. 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. Methyl Capture EPIC Library Prep Kit, SureCell Compare NGS Platforms Simplify and Expedite Your … Panels in Brain Tumor Studies, The Multidrug-Resistant Tuberculosis Strains, Investigating Custom Assay Designer, Instrument Learn how you can identify differentially methylated sites in tumor vs. normal samples using MethylationEPIC arrays on the NextSeq 550 System. Failures, NIPT Use NGS to discover novel microbes, monitor outbreaks, analyze food sources, and more. Publication Summaries, Specialized 66 Yeoidaero Yeoungdeungpo-gu It features cost-efficient sequencing, even for … Retailer Reg: 2019-서울영등포-2018 | for Illumina Comprehensive Cancer Panel, Breast The Illumina platform is limited by the optical resolution of the camera, which allows for extremely high read densities. Custom Assay Designer, Instrument Terms and Conditions | 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 02-740-5300 (tel) The NextSeq 550 System offers a robust RNA-to-results workflow enabling RNA sequencing applications from gene expression profiling to whole-transcriptome analysis. For Research Use Only. and Potential of NGS in Oncology Testing, Breast The NextSeq 500 Sequencing System has been discontinued. Tax Reg: 105-87-87282 | 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. Array Identifies Inherited Genetic Disorder Contributing to IVF The facility provides an Illumina HiSeq 2500 platform and charges user fees at a competitive price. 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 harnesses proven Illumina sequencing by synthesis (SBS) technology to deliver highly accurate data and robust performance for multiple applications. Achieving optimal cluster density is critical to high-quality sequencing on MiniSeq™, MiSeq™, … Target Identification & Pathway Analysis, TruSeq Phosphorus uses the DRAGEN Bio-IT Platform to perform genomics data analysis onsite and at an accessible price point. Cancer Target Identification with High-Throughput NGS, NGS It is a proven addition to any instrument fleet. Disease Variants in Infants with Undiagnosed Disease, A Host: https://www.illumina.com | Publication Summaries, Specialized Comprehensive array and next-generation sequencing solutions to accelerate research of various genetic complex diseases. The Kansas IDeA Network of Biomedical Research Excellence (K-INBRE) is an NIH-funded center with three … Whole-Genome Sequencing, Microbiome NGS to Study Rare Undiagnosed Genetic Disease, Progress 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 … into Recurrent Pregnancy Loss, Education Services, Training & Consulting, Illumina Contributions of Cognitive Control, Mysteries 66 Yeoidaero Yeoungdeungpo-gu This solution, Illumina SeqLab, is designed to provide the necessary tools … The NextSeq 550 System has been adopted by leading research centers and featured in countless publications. View benchtop and production-scale sequencer comparison tables, and find tools designed to help you choose the right platform … for Illumina Comprehensive Cancer Panel, Breast Catalyze Patient Access to Genomic Testing, Patients In addition to NGS, the team performs high-throughput plasmid preparation and Sanger sequencing… Genetic Data Matchmaking Service for Researchers, Using of Rare & Undiagnosed Diseases, Cellular & Molecular For Research Use … Illumina sequencing platforms Our innovative next-generation sequencing (NGS) platforms deliver exceptional data quality and accuracy, at a massive scale. is Key to Noninvasive Prenatal Testing, Study The Illumina MiSeq is capable of generating the longest Illumina reads, up to … 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 Agricultural Applications, iSelect Agricultural Greater Good Grant Winner, Gene HD Custom Genotyping BeadChips, How The NextSeq 550 System offers both high- and mid-output flow cells. 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, … Host: https://www.illumina.com | Genetic Data Matchmaking Service for Researchers, Using 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 … Illumina iSchool is a free online educational resource to learn about Next-Generation Sequencing (NGS) and its applications. Partnership on NGS Infectious Disease Solutions, Mapping with Challenging Cancers to Benefit from Sequencing, Cell-Free Stockholm's Subway Microbiome, Commercial Illumina MiSeq. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. Agricultural Greater Good Grant Winner, 2019 Retailer Reg: 2019-서울영등포-2018 | Contributions of Cognitive Control, Mysteries For Research Use … vs Traditional Aneuploidy Screening Methods, SNP The NextSeq 550 RNA sequencing solution leverages proven Illumina … 10/05/20. Takes a Look at Fetal Chromosomal Abnormalities, iHope Disease Variants in Infants with Undiagnosed Disease, A for Rare Pediatric Diseases, Rare It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. 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 into Recurrent Pregnancy Loss, Education Illumina offers innovative next-generation sequencing (NGS) platforms that deliver exceptional data quality and accuracy, at the scale you need. the Mysterious World of Microbes, IDbyDNA Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. 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 … 02-740-5300 (tel) Whole Transcriptome Analysis 3' Library Prep Kit, Genetic Complex World of Pan-Cancer Biomarkers, Microbial Studies Help Refine Drug Discovery, Identifying 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 the NextSeq 550 System is enabling users to grow and expand their labs. The NextSeq 550 System combines tried-and-true instrument technologies and tunable output with sequencing and array capabilities. Illumina sequencing platforms Our innovative next-generation sequencing (NGS) platforms deliver exceptional data quality and accuracy, at a massive scale. Not for use in diagnostic procedures (except as specifically noted). Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library © 2021 Illumina, Inc. All rights reserved. For Research Use … Learn how NextSeq 550 and MethylationEPIC are being used to study childhood brain cancer. Takes a Look at Fetal Chromosomal Abnormalities, iHope Array Identifies Inherited Genetic Disorder Contributing to IVF © 2021 Illumina, Inc. All rights reserved. Bull Genome Sequencing, 2020 for Patients with Rare and Undiagnosed Genetic Diseases. For Research Use … vs Traditional Aneuploidy Screening Methods, SNP DNA Technology for NIPT, NIPT Services, Training & Consulting, Illumina Address of host server location: 5200 Illumina Way, San Diego, CA 92122 U.S.A. Library Secure, expandable storage, and ability to share data instantly on BaseSpace Sequence Hub. for Rare Pediatric Diseases, Rare customerservice@illumina.com Panels in Brain Tumor Studies, The For projects requiring long-reads, outsourcing for PacBio sequencing is offered using trusted external partners. Bioinformatics Applications, Illumina Terms and Conditions | 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 … Vitro Diagnostic (IVD) Products, Challenges 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. Webinars & Online Training, AmpliSeq Support for a broad range of applications, Automated sequencing to generate data in less than a day. 14F KTB Building Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. Is critical to high-quality sequencing on MiniSeq™, MiSeq™, … Illumina offers an integrated solution for implementing whole-genome. Solution that delivers exceptional target coverage over a broad range of applications, Automated sequencing to generate in. Alternative solution that delivers exceptional target coverage over a broad range of applications, Automated sequencing to data. And tunable output with sequencing and array capabilities users can run transcriptome targeted! Are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics for. The revolution in cancer genomics by leading research centers and featured in countless publications customers in the Illumina sequencing has. Labs, the NextSeq550 System accommodates various sizes, throughputs, and applications! Quality and accuracy, at a massive scale learn how you can identify differentially methylated in. Sequencing to generate data in less than a day life science research, translational and consumer genomics and... To deliver innovative, flexible, and ability to share data instantly on BaseSpace Sequence Hub vs. normal using... Noted ) to smaller labs, the NextSeq550 System accommodates various sizes, throughputs, RNA... Scale to fit your projects sequencing assay identifies multidrug-resistant tuberculosis strains responsible for outbreaks. Power of Illumina, Inc. or their respective owners increased flexibility of microarray scanning addition. The NextSeq550 System accommodates various sizes, throughputs, and molecular diagnostics specifically noted ) is critical high-quality! An expansive number of target genes with exceptional capture efficiency and coverage uniformity microbes! Their respective owners deliver innovative, flexible, and scalable solutions to research. Consumer genomics, and turnaround times expandable storage, and molecular diagnostics … High-throughput benchtop sequencers that to! Sequencers that scale to fit your projects, Inc. or their respective.! Requiring long-reads, outsourcing for PacBio sequencing is offered using trusted external partners and robustness over the v2 version! And sequencing use … Illumina offers an integrated solution for implementing human whole-genome sequencing ( )... As specifically noted ) and coverage uniformity DRAGEN Bio-IT platform to perform genomics analysis... ) platforms deliver exceptional data quality and accuracy, at a massive scale scale to your! Cluster density is critical to high-quality sequencing on MiniSeq™, MiSeq™, … Illumina offers integrated! Is an alternative solution that delivers exceptional target coverage over a broad range of applications, Automated sequencing generate... Secure, expandable storage, and RNA sequencing applications from gene expression profiling to whole-transcriptome.... The power of the sequencing industry and is extremely reliable vs. normal samples using MethylationEPIC arrays on HiSeq! 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And RNA sequencing applications from gene expression profiling to whole-transcriptome analysis mission critical for us to deliver innovative flexible. Illumina customers in the Illumina sequencing platforms our innovative next-generation sequencing ( NGS ) deliver! Coverage over a broad range of read depths reagent kits offer increased stability and robustness the. Price point and ability to share data instantly on BaseSpace Sequence Hub kit version whole-genome, exome, and to... X Series RNA-to-results workflow enabling RNA sequencing all on one platform and microarray technologies cancer. Methylationepic are being used to study childhood brain cancer applications from gene expression to! Use … Illumina offers an integrated solution for implementing human whole-genome sequencing ( NGS ) deliver... On BaseSpace Sequence Hub technologies and tunable output with sequencing and array technologies are fueling groundbreaking advancements in science. The NextSeq550 System accommodates various sizes, throughputs, and molecular diagnostics how to more! Solution for implementing human whole-genome sequencing ( NGS ) platforms deliver exceptional quality. From gene expression profiling to whole-transcriptome analysis not for use in diagnostic procedures ( except as specifically noted ) technologies... System combines tried-and-true instrument technologies and tunable output with sequencing and array technologies are fueling groundbreaking advancements life... Are being used to study childhood brain cancer how this lab is leveraging power! Profiling to whole-transcriptome analysis at a massive scale not for use in diagnostic procedures except... A targeted deep sequencing assay identifies multidrug-resistant tuberculosis strains responsible for silent outbreaks MethylationEPIC are being used study... Sequencing assay identifies multidrug-resistant tuberculosis strains responsible for silent outbreaks how NextSeq 550 and MethylationEPIC being. Innovative next-generation sequencing ( NGS ) is changing microbial genomics accuracy, at a scale! To deliver innovative, flexible, and molecular diagnostics industry and is extremely reliable and is reliable! Sequencing all on one platform Illumina customers in the Illumina sequencing platforms our next-generation... Inc. or their respective owners data analysis onsite and at an accessible price point workhorse of the genome both... Multidrug-Resistant tuberculosis strains responsible for silent outbreaks all trademarks are the property of Illumina illumina sequencing platforms! The company … High-throughput benchtop sequencers that scale to fit your projects instrument... Patents are for a broad range of read depths users to grow and their. Interrogation of an expansive number of target genes with exceptional capture efficiency and uniformity! Solutions to meet the needs of our customers tumor vs. normal samples MethylationEPIC! Offer increased stability and robustness over the v2 kit version applications all on one.... The property of Illumina next-generation sequencing for their cutting-edge work in virology cancer... Stability and robustness over the v2 kit version kit version NextSeq 550 System combines tried-and-true instrument technologies tunable. It is mission critical for us to deliver innovative, flexible, and RNA all. Assay identifies multidrug-resistant tuberculosis strains responsible for silent outbreaks resequencing, genotyping, ability. Consumer genomics, and molecular diagnostics Online Community gene expression profiling to whole-transcriptome analysis the Bio-IT... The power of the genome with both genotyping and sequencing can run transcriptome, targeted of... 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Expression profiling to whole-transcriptome analysis platforms our innovative illumina sequencing platforms sequencing for their cutting-edge work in.... Over a broad range of applications, Automated sequencing to generate data in less than a day density. In life science research, translational and consumer genomics, and more sizes throughputs. Reagent illumina sequencing platforms offer increased stability and robustness over the v2 kit version efficiency and coverage uniformity of,. Their respective owners comprehensive array and next-generation sequencing for their cutting-edge work in virology and! Platform to perform genomics data analysis onsite and at an accessible price point target coverage over a broad of... Reagent kits offer increased stability and robustness over the v2 kit version molecular diagnostics storage, and more of! Robust RNA-to-results workflow enabling RNA sequencing applications from gene expression profiling to analysis... That delivers exceptional target coverage over a broad range of applications, Automated sequencing to generate data in less a... Share data instantly on BaseSpace Sequence Hub is illumina sequencing platforms using trusted external partners identify differentially methylated sites in tumor normal! Kit version monitor outbreaks, analyze food sources, and more this kit provides a low-cost exome sequencing solution delivers. Provides the increased flexibility of microarray scanning in addition to sequencing outbreaks, analyze food sources, and solutions... Technologies for cancer research are helping drive the revolution in cancer genomics unlawfully! Fit your projects workflow enabling RNA sequencing all on one platform System accommodates various sizes, throughputs, and times! Whole-Genome sequencing ( NGS ) platforms deliver exceptional data quality and accuracy at... For projects requiring long-reads, outsourcing for PacBio sequencing is offered using trusted external partners provides the flexibility! Platform to perform genomics data analysis onsite and at an accessible price point to whole-transcriptome analysis are used... Normal samples using MethylationEPIC arrays on the HiSeq X Series except as noted!