- MyIllumina
- Tools
Highlights
Superior Accuracy and Throughput
Billions of bases per week with the highest percentage of perfect reads
Fast, Streamlined Workflow
Sample to data in less than one week
Broadest Range of Applications
Whole genome and de novo sequencing, targeted resequencing, transcriptomic and epigenetic analysis and more
New Products & Platforms
Featured Research Papers
- High definition profiling of mammalian DNA methylation by array capture and single molecule bisulfite sequencing. Hodges E et al. 2009.
- Repertoire of bovine miRNA and miRNA-like small regulatory RNAs expressed upon viral infection. Glazov EA et al. 2009.
- Identification of Nutrient-Responsive Arabidopsis and Rapeseed MicroRNAs by Comprehensive Real-Time Polymerase Chain Reaction Profiling and Small RNA Sequencing. Pant BD et al. 2009.
- Profiling the T-cell receptor beta-chain repertoire by massively parallel sequencing. Freeman JD et al. 2009.
Workflow
Simple workflow. Single-user operation.
System automation. Turnkey operation. The simple sequencing workflow enables even small labs to have sequencing capabilities rivaling those of genome centers. With the fastest and least labor-intensive workflow of any sequencing technology, your lab can generate highly accurate results in under a week. Automation frees you to complete groundbreaking studies in minimal time. Simplified process. Minimized hands-on time. It’s genomic power for everyone.
HiSeq Workflow
Applications
DNA Sequencing
Perform whole-genome or de novo sequencing, targeted resequencing, SNP discovery, and identification of copy number variations and chromosomal rearrangements using Illumina's massively parallel sequencing technology. Illumina sequencing features industry-leading read lengths, the highest raw read accuracy, and the flexibility of insert size and paired-end protocols, enabling the broadest range of genomic sequencing applications.
Whole Genome Sequencing – using the Illumina Genome Network
The Illumina Genome Network links researchers interested in conducting large whole human genome sequencing projects with leading institutes worldwide that provide highly economical and rapid turnaround access to Illumina sequencing.
Transcriptome Analysis
Explore the transcriptome like never before with Illumina sequencing. Characterize transcriptional activity and reveal the hidden world of RNA architecture without prior information using Illumina's unique combination of long and short reads and millions of counts. Analyze strand-specific mRNA, annotate coding SNPs, discover transcript isoforms, identify regulatory RNAs, characterize splice junctions and determine transcript abundance.
Gene Regulation Analysis
Accurately survey epigenetic interactions and their effects on gene expression central to many biological processes and disease states. Quantify in vivo protein-DNA interactions on a genome-wide scale using chromatin immunoprecipitation with Illumina sequencing technology (ChIP-Seq). Characterize the methylome to single base resolution by sequencing bisulfite-treated DNA.
Software
Open Architecture. Streamlined Analysis.
Powerful Software. Easy-to-use Interface.
Our suite of integrated applications is built to go from image capture to interactive analysis in real time. Quickly and easily assess the success of your run. Customize your workflow engine with our flexible architecture. It's massive-scale data analysis, simplified.
Genome Analyzer Pipeline and CASAVA
- Drives primary data analysis and transforms data into biologically relevant information.
- Produces intensity scores, base calls with calibrated quality metrics, and quality-scored alignments.
- Creates genomic builds, calls SNPs, and counts reads from data generated from one or more sequencing runs.
- Enables easy customization for the throughput requirements of any lab.
GenomeStudio Software
- Facilitates exploration of data from multiple genetic analysis applications.
- Enables the comparison and correlation of data from all Illumina platforms.
- Allows you to obtain a complete picture of the genome and identify potential disease targets.
Learn more about Illumina-evaluated software tools and other third-party Genome Analyzer data analysis solutions.
At Illumina, our goal is to apply innovative technologies and revolutionary assays to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. These studies will help make the realization of personalized medicine possible. With such rapid advances in technology taking place, it is mission critical to have solutions that are not only innovative, but flexible, scalable, and complete with industry-leading support and service. As a global company that places high value on collaborative interactions, rapid delivery of solutions, and prioritizing the needs of its customers, we strive to meet this challenge. Illumina's innovative, array-based solutions for DNA, RNA, and protein analysis serve as tools for disease research, drug development, and the development of molecular tests in the clinic.