MiSeq i100 Series cancer research

Faster cancer research insights

Unrivaled simplicity, unthinkable turnaround time in your lab

Female scientist using a single pipette to prepare the flow cell for loading, with the MiSeq i100 instrument in the foreground and a purple-blue status bar showing the run in progress

Bring powerful insights into your lab

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.

Female scientist using finger to make a selection from the start touch screen monitor while looking at the finish screen on another instrument. Angled side view of person and instruments on lab bench.

Powerful, simple sequencing

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.

Accurate sequencing with same-day results

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.

  • Rapid turnaround
  • Targeted profiling studies
  • Simplified workflow
  • Onboard analysis
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A wide range of cancer research applications

Targeted sequencing for cancer research studies

Learn more about streamlined, accessible workflows with focused NGS panels that provide insights into cancer biology with the cancer research methods guide.

Featured cancer research workflow

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Library Prep
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Sequencing
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Data analysis
Profile image of male and female scientists reviewing the run setup screen

NGS Workflow Finder

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.

FAQ

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.

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Related content

Cancer research

Our sequencing and microarray technologies support a broad range of cancer genomics research applications, including DNA to RNA analysis, epigenetics, and more.

Targeted sequencing

With targeted sequencing or resequencing, a subset of genes or a genomic region of interest is isolated and sequenced, which can conserve lab resources.

Speak to a specialist

Talk to an expert about adopting the MiSeq i100 Series for your cancer research.