High-accuracy NGS with the MiSeq i100 Series
This application note compares data generated using targeted panels for cancer research on the MiSeq i100 Series and the MiSeq System.
With the MiSeq i100 Series, obtaining high-quality reliable results for targeted DNA and RNA sequencing research applications is faster and easier than ever before. Facilitate the identification of key variants, such as single nucleotide variant (SNVs), insertions/deletions (indels), gene fusions, copy number alterations, and other genomic aberrations that drive tumorigenesis and progression.
Access the simplest, fastest benchtop sequencing with the MiSeq i100 Series, providing meaningful insights for cancer research by identifying key mutations and other genomic aberrations that underlie tumorigenesis with the MiSeq i100 Series.
Next-generation sequencing (NGS) has transformed the landscape of cancer research with its remarkable precision and extensive genomic analysis capabilities. Analyze a broad range of genetic information—including novel mutations and low-frequency events—in as little as four hours.
Build out your NGS capabilities with the MiSeq i100 Series for the simplest, fastest benchtop sequencing solution imaginable. Increase your lab’s insights into cancer progression today by researching key genomic alterations.
High-accuracy NGS with the MiSeq i100 Series
This application note compares data generated using targeted panels for cancer research on the MiSeq i100 Series and the MiSeq System.
Illumina cancer research workflow solutions
Illumina offers a comprehensive portfolio of cancer research workflow solutions designed to help laboratories generate high-quality, reproducible genomic insights.
Targeted cancer research workflow with Pillar Biosciences and Illumina
Rapid, accurate results with oncoReveal panels on the MiSeq i100 Series, analyzed and reported with DRAGEN Amplicon.
Learn more about streamlined, accessible workflows with focused NGS panels that provide insights into cancer biology with the cancer research methods guide.
fireflyGO automated liquid handler
Automated library preparation for rapid, streamlined NGS workflows with fewer touchpoints and reduced errors.
Pillar oncoReveal panels use next-generation sequencing to enable fast, targeted cancer research across diverse sample types.
Simplified operations and system install, advanced chemistry, and onboard informatics provide an easy-to-use, fast, flexible, and reliable system supporting cancer research applications.
Amplicon-optimized secondary analysis for accurate DNA/RNA variant detection, fusion calling, and rapid research insights.
The NGS workflow tool can help you find the right workflow for your cancer research using our predesigned workflows or by building your own.
The MiSeq i100 Series has significantly improved our workflow with faster run times and a streamlined setup, enabling more timely results.
The MiSeq i100 Series is well suited for targeted translational cancer research workflows such as targeted DNA variant analysis, RNA fusion detection, solid tumor profiling, hematologic malignancy research, hereditary cancer research, liquid biopsy and cfDNA studies, and cancer biomarker discovery.
The MiSeq i100 Series makes targeted cancer sequencing studies fast, simple, and accessible without sacrificing data quality. MiSeq i100 Series can do same-day targeted DNA and RNA sequencing for solid tumors, hematologic malignancies, hereditary cancer, and liquid biopsy research with simplified workflows and onboard analysis.
The MiSeq i100 Series was designed for both new and experienced users with its streamlined operations, from easy setup to onboard data analysis. Run setup requires only three steps and can be completed in less than 20 minutes. Integrated reagent cartridges offer room temperature ship and storage. Data analysis summaries can be generated in two hours or less for most applications by accessing preconfigured DRAGEN pipelines, either onboard or in the cloud, requiring minimal bioinformatics expertise.
The MiSeq i100 Series has a streamlined workflow that includes expedited setup with room-temperature consumables and intuitive data analysis. Research workflows are available for targeted sequencing of solid and hematological malignancies. Onboard DRAGEN secondary analysis reduces turnaround times to deliver same-day results. Watch how easy it is to set-up a run on the MiSeq i100 Series.
Pillar oncoReveal panels are specifically designed to leverage the MiSeq i100 Series ultrafast turnaround times for somatic mutation profiling studies. For germline research, the TruSight Hereditary Cancer Panel is fully compatible with the MiSeq i100 Series. AmpliSeq for Illumina is ideal for custom-designed small panels or specialized hotspots where you only want to sequence a handful of specific candidate genes.
Our sequencing and microarray technologies support a broad range of cancer genomics research applications, including DNA to RNA analysis, epigenetics, and more.
With targeted sequencing or resequencing, a subset of genes or a genomic region of interest is isolated and sequenced, which can conserve lab resources.
Talk to an expert about adopting the MiSeq i100 Series for your cancer research.