Similar documents
MiSeq. system applications

High-throughput scale. Desktop simplicity.

NextSeq 500 System WGS Solution

The Expanded Illumina Sequencing Portfolio New Sample Prep Solutions and Workflow

Introduction to the MiSeq

The MiniSeq System. Explore the possibilities. Discover demonstrated NGS workflows for molecular biology applications.

resequencing storage SNP ncrna metagenomics private trio de novo exome ncrna RNA DNA bioinformatics RNA-seq comparative genomics

ILLUMINA SEQUENCING SYSTEMS

Introduction to the NextSeq System

Illumina s Suite of Targeted Resequencing Solutions

Meet the iseq 100 System.

Total genomic solutions for biobanks. Maximizing the value of your specimens.

DNA. bioinformatics. genomics. personalized. variation NGS. trio. custom. assembly gene. tumor-normal. de novo. structural variation indel.

How much sequencing do I need? Emily Crisovan Genomics Core

How much sequencing do I need? Emily Crisovan Genomics Core September 26, 2018

Genomic solutions for complex disease

Introducing QIAseq. Accelerate your NGS performance through Sample to Insight solutions. Sample to Insight

G E N OM I C S S E RV I C ES

HiSeqTM 2000 Sequencing System

Overcome limitations with RNA-Seq

High Throughput Sequencing the Multi-Tool of Life Sciences. Lutz Froenicke DNA Technologies and Expression Analysis Cores UCD Genome Center

Illumina Technology Updates

Next-Generation Sequencing: custom solutions

Getting high-quality cytogenetic data is a SNP.

DNA. bioinformatics. epigenetics methylation structural variation. custom. assembly. gene. tumor-normal. mendelian. BS-seq. prediction.

solid S Y S T E M s e q u e n c i n g See the Difference Discover the Quality Genome

Deep Sequencing technologies

The New Genome Analyzer IIx Delivering more data, faster, and easier than ever before. Jeremy Preston, PhD Marketing Manager, Sequencing

Wet-lab Considerations for Illumina data analysis

Genome Resequencing. Rearrangements. SNPs, Indels CNVs. De novo genome Sequencing. Metagenomics. Exome Sequencing. RNA-seq Gene Expression

High Throughput Sequencing the Multi-Tool of Life Sciences. Lutz Froenicke DNA Technologies and Expression Analysis Cores UCD Genome Center

Illumina Custom Capabilities: Amplicons, Enrichment and iselect

02 Agenda Item 03 Agenda Item

Next-generation sequencing technologies

EpiGnome Methyl-Seq - DNA Methylation Analysis using Whole Genome Bisulfite Sequencing

Ion S5 and Ion S5 XL Systems

Ion S5 and Ion S5 XL Systems

Illumina Sequencing Overview

ngs metagenomics target variation amplicon bioinformatics diagnostics dna trio indel high-throughput gene structural variation ChIP-seq mendelian

Surely Better Target Enrichment from Sample to Sequencer

SEQUENCING FROM SAMPLE TO SEQUENCE READY

Genomic & RNA Profiling Core Facility

High Throughput Sequencing the Multi-Tool of Life Sciences. Lutz Froenicke DNA Technologies and Expression Analysis Cores UCD Genome Center

About Strand NGS. Strand Genomics, Inc All rights reserved.

Bioinformatics Advice on Experimental Design

GENOMICS WORKFLOW SOLUTIONS THAT GO WHERE THE SCIENCE LEADS. Genomics Solutions Portfolio

TREE CODE PRODUCT BROCHURE

Welcome to the NGS webinar series

FRAUNHOFER INSTITUTE FOR INTERFACIAL ENGINEERING AND BIOTECHNOLOGY IGB NEXT-GENERATION SEQUENCING. From wet lab to dry lab complete sample analysis

Considerations for Illumina library preparation. Henriette O Geen June 20, 2014 UCD Genome Center

Introduction to Microbial Sequencing

Matthew Tinning Australian Genome Research Facility. July 2012

Genomic Information Revolution(s)

Welcome at Your Automation Partner. Automation solutions for NGS in Forensic DNA research. Willem van Loon

Genome Analyzer. RNA ChIP

Enabling New Markets for Growth Empowering the Genomics Revolution

Introduction. Highlights. Prepare Library Sequence Analyze Data

Experimental Design Microbial Sequencing

Admera Health RUO Services

Transcriptomics analysis with RNA seq: an overview Frederik Coppens

Applications of Next Generation Sequencing in Metagenomics Studies

Microbial sequencing solutions

Accessible answers. Targeted sequencing: accelerating and amplifying answers for oncology research

GENOMICS WORKFLOW SOLUTIONS THAT GO WHERE THE SCIENCE LEADS. Genomics Solutions Portfolio

NEXT GENERATION SEQUENCING. Farhat Habib

Next Generation Sequencing. Target Enrichment

Ion S5 and Ion S5 XL Systems

Gene Regulation Solutions. Microarrays and Next-Generation Sequencing

Increased transcription detection with the NEBNext Single Cell/Low Input RNA Library Prep Kit

Next-generation sequencing technologies

Surely Better Target Enrichment from Sample to Sequencer and Analysis

CM581A2: NEXT GENERATION SEQUENCING PLATFORMS AND LIBRARY GENERATION

Whole Transcriptome Analysis of Illumina RNA- Seq Data. Ryan Peters Field Application Specialist

Research school methods seminar Genomics and Transcriptomics

Impact of gdna Integrity on the Outcome of DNA Methylation Studies

Automation of Lexogen s QuantSeq 3 mrna-seq Library Prep Kits on the Biomek FX p NGS Workstation

Single Cell Genomics

Lecture 7. Next-generation sequencing technologies

TruSeq Nano DNA Library Prep Protocol Guide

Parts of a standard FastQC report

Basics of RNA-Seq. (With a Focus on Application to Single Cell RNA-Seq) Michael Kelly, PhD Team Lead, NCI Single Cell Analysis Facility

Gene expression microarrays and assays. Because your results can t wait

Illumina TruSeq RNA Access Library Prep Kit Automated on the Biomek FX P Dual-Hybrid Liquid Handler

Throughput cells cells. Methodology Full transcript or end-counting end-counting. Chemistry SMARTer V SMARTer V. Run time hours.

Illumina Microarray Solutions. A complete range of microarrays for every need.

In vivo genome-wide profiling of RNA secondary structure reveals novel regulatory features

Next Generation Sequencing. Tobias Österlund

PCR Seeing Science in. Everything We Do. Amplification. Systems. Solutions for Genomics Researchers

Aaron Liston, Oregon State University Botany 2012 Intro to Next Generation Sequencing Workshop

TruSight Cardio Sequencing Kit Protocol Guide

Titelstijl van model bewerken

Applications of short-read

Integrated NGS Sample Preparation Solutions for Limiting Amounts of RNA and DNA. March 2, Steven R. Kain, Ph.D. ABRF 2013

Comprehensive. Flexible. Personalized. Illumina Product Support Services Customized service to meet your needs

HIR Central Lab High End Instrument

Understanding the science and technology of whole genome sequencing

NGS-based innovations within the Leiden Network

Single-Cell. Defy the Law of Averages

PacBio. The world s first single molecule, real-time DNA sequencer

NGS part 2: applications. Tobias Österlund

Transcription:

www.illumina.com/hiseq www.illumina.com FOR RESEARCH USE ONLY 2012 2014 Illumina, Inc. All rights reserved. Illumina, BaseSpace, cbot, CSPro, Genetic Energy, HiSeq, Nextera, TruSeq, the pumpkin orange color, and the Genetic Energy streaming bases design are trademarks or registered trademarks of Illumina, Inc. All other brands and names contained herein are the property of their respective owners. Pub. No. 770-2012-003 Current as of 20 December 2013

HiSeq 2500 applications

Production power. Power and efficiency for large-scale genomics across a wide array of applications. The advent of next-generation sequencing (NGS) has accelerated genomics at a spectacular pace. The first complete human genome was sequenced in 2003 a feat requiring over 10 years, hundreds of sequencers, and the collaboration of dozens of laboratories around the world. Now NGS has taken us from a genome in a decade to a genome in a day on the HiSeq 2500 System. Our dedication to making sequencing accessible to everyone has helped drive innovation forward. The HiSeq 2500 System gives you the flexibility to go from multiple genomes in a run, to the fastest whole genome yet. The HiSeq System provides a high-powered, cost-effective solution for large, production-scale projects. Empower your research like never before. Any application. Any study. Any sample size. From sample prep through data analysis, we focus on making applications easy so you can stay focused on your research. Targeted resequencing, gene expression, whole-genome sequencing, epigenetics, and more we ve designed simple, end-to-end solutions for any study. No matter your lab size, research goal, or scale of study.

Simplest workflow for all applications. Integrated solutions. Streamlined operation. From sample preparation to data analysis, the HiSeq 2500 is a proven and efficient powerhouse for large-scale genomics. Empowering labs to rapidly and cost-effectively take on a broad range of projects. Easy sample preparation and enrichment Access a family of reagent kits that provide the industry s fastest and simplest workflows for preparing DNA or RNA samples. Powerful sequencing flexibility Scale the instrument output to fit your immediate sequencing needs. Choose between rapid-run mode for fast results or highoutput mode for more samples. Proven data analysis solutions Go from raw data to meaningful results. Plug into integrated data analysis tools. With our cloud-based computing environment, BaseSpace, or onsite data processing system, IlluminaCompute, labs can become fully operational in weeks rather than months without pre-existing IT infrastructure. Sample Preparation Sequence Analyze The HiSeq System offers a complete, integrated workflow from sample preparation though data analysis.

Whole-genome sequencing. Quickly and cost-effectively sequence genomes right in your lab with the HiSeq 2500. Accelerate turnaround time with rapid run mode or, stay in high output mode and sequence multiple genomes in a single run. Both modes produce the industry s highest data quality, for the most accurate and complete whole-genome sequencing results. Targeted resequencing. From whole exome analysis to custom enrichment panels, choose from a comprehensive suite of targeted resequencing solutions to support any study design. Scalable discovery and cost-effective validation or screening are now at your fingertips. Whole-transcriptome sequencing. From high-throughput gene expression profiling to deep transcriptional analysis, HiSeq offers unprecedented RNA analysis solutions. Measure abundance of individual transcripts and isoforms, discover new genes, and identify regulatory non-coding RNAs. De novo sequencing and metagenomics. With a unique mix of high output, long reads, and paired-end sequencing, the HiSeq is a powerful tool for de novo sequencing of any size genome. Perform true metagenomic analyses by sequencing entire microbial communities to discover important taxonomic and functional information. Regulation Epigenetics and gene regulation. Get a more complete biological story by assessing multiple forms of epigenetic regulation in a single HiSeq run. Study DNA-protein interactions and gene regulation using ChIP-Seq. Quantify DNA methylation down to single base resolution. ChIP-Seq

RNA-Seq Amplicon ChIP-Seq Targeted ChIP-Seq RNA-Seq de novo RNA-Seq de novo RNA de novo ChIP-Seq RNA Targeted Small Genome RNA Targeted Custom Enrichment Small Genome Sm Se RNA Custom Small RNA Enrichment Small Genome R Clone Checking Small RNA Small Genome Custom Enrichment Custom Enrichment Targeted 16S Metagenomics Plasmid RNA-Seq Targeted Small RNA Custom Enrichment Regulation de novo Regulation

Proven Illumina SBS technology. Highest accuracy at any coverage level. Illumina sequencers are the most trusted and widely adopted worldwide for a reason: proven Illumina SBS technology delivers the highest data quality in the industry. Illumina SBS technology supports an unprecedented range of genomic applications, with exceptional data accuracy. It ensures the highest standard of quality for any research project empowering you to drive your research forward with the maximum confidence. Highest quality data when answers matter. Millions of Bases 16000 14000 12000 10000 8000 6000 4000 HiSeq 2500 generates the highest percentage and yield of data > Q30. 2000 10 20 30 40 Q Score Quality scores from a human genome, single flow-cell run sequenced in 27 hours, in rapid-run mode, with > 92% of bases above Q30, and 99.9% accuracy.

The broadest range of sequencing applications. From whole-genome sequencing to small RNA sequencing, the HiSeq 2500 offers accurate, fast, and cost-effective solutions for any NGS application. Application Recommended Read Length Optimized Kits Whole-Genome TruSeq DNA PCR-Free Sample Prep Kit 2 100 125 TruSeq Nano DNA Sample Prep Kit Nextera DNA Sample Prep Kit TruSeq DNA PCR-Free Sample Prep Kit De Novo 2 100 125 TruSeq Nano DNA Sample Prep Kit Nextera Mate Pair Sample Prep Kit Targeted DNA Exome Enrichment 2 75 100 Nextera Rapid Capture Exome Kit Nextera Rapid Capture Expanded Exome Kit Custom Enrichment 2 75 Nextera Rapid Capture Custom Kit RNA RNA-Seq (Expression Profiling) 1 50 TruSeq Stranded mrna Sample Prep Kit RNA-Seq (Whole Transcriptome) 2 75 TruSeq Stranded mrna Sample Prep Kit TruSeq Stranded Total RNA Sample Prep Kit Regulation Applications ChIP-Seq 1 50 TruSeq ChIP Sample Prep Kit Methylation Analysis 2 75 Epicentre EpiGnome Methyl-Seq Kit

HiSeq 2500 applications Empower your research with HiSeq. Learn more at www.illumina.com/hiseq