Explore genomic solutions to drive breakthroughs in cancer for a better tomorrow
Cancer is a complex, multifactorial disease that causes uncontrolled growth of cells, which can spread throughout the body from where they first formed. Interactions between cancer cells and their microenvironments affect every aspect of the cancer cell, including the genome, epigenome, transcriptome, and proteome. Thanks to advanced tools like next-generation sequencing (NGS) and microarrays, experts are using their unprecedented understanding of cancer biology to make meaningful advances in research, personalized medicine, and more.
NGS allows researchers to detect low-frequency molecular events associated with carcinogenesis, cancer growth, and metastasis without bias for novel discoveries. Our comprehensive product portfolio supports integrated and flexible workflow solutions for library preparation, sequencing, and analysis to study DNA, RNA, epigenetics, protein, and more to enable multiomic cancer research. We offer a range of sequencing systems to meet your needs, from powerful benchtop models to versatile, high-throughput sequencing platforms to deliver quick, accurate, and cost-effective answers for actionable insights.
The Cancer Research Methods Guide is a 40+ page resource with simple, comprehensive workflows for a broad range of cancer research applications. This guide discusses single-cell sequencing, spatial sequencing, methylation profiling, multiomics, cell-free RNA sequencing, and more.
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NGS allows researchers to detect low-frequency molecular events associated with carcinogenesis, cancer growth, and metastasis without bias for novel discoveries. The comprehensive product portfolio supports integrated and flexible workflow solutions for library preparation, sequencing, and analysis to study DNA, RNA, epigenetics, protein, and more to enable multiomic cancer research. We offer a range of sequencers to meet your needs, from powerful benchtop sequencers to versatile, high-throughput systems to deliver quick, accurate, and cost-effective answers for actionable insights.
Explore cancer sequencing methods and learn about the benefits of combining different omic studies to deepen your cancer research insights. See how cancer research applications can expand your understanding of complex disease mechanisms.
Cancer whole-genome sequencing
Explore benefits and methods for comprehensive cancer whole-genome sequencing.
Learn more about the advantages of whole-exome sequencing for efficient analysis of the coding region to streamline your cancer research.
Cancer transcriptome sequencing
Analyze gene expression to further your understanding of gene expression variants, mutational profiles, and more for cancer research.
See how to capture nongenetic changes that can influence phenotypes with NGS-based techniques.
Learn about the latest advancements in cancer detection, characterization, and analysis using NGS for various cancer research applications.
Learn how to use NGS to study immunotherapy response factors, discover biomarkers, and apply genomics to personalized immunotherapy.
Resolve cancer samples at the single-cell level for detailed insights into the complex biology of cancer.
See how NGS can be combined with liquid biopsy research to detect and characterize various cancer-derived biomarkers.
See how you can use multiomics to better connect genotype to phenotype and obtain a full cellular readout not found through single omic approaches.
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Explore videos and resources advancing cancer biology and research using NGS techniques and applications.
Advancing cancer research with multiomics
See the video to learn how researchers at the Ontario Institute for Cancer Research and United Health Network link complex phenotypes through multiomics to enable discoveries that weren’t possible before.
Single-cell multiomics beyond RNA-Seq
In this webinar, Dr Michael Kelly discusses the use of single-cell and spatial technologies to advance basic science and translational research.
Redefining possibilities in cancer research
Watch this webinar to learn more about instrument-free approaches, from single-cell studies through single-workflow multiomic sequencing and analysis, for cancer research.
lllumina offers comprehensive NGS- and array-based solutions for cancer research to accommodate multiple study needs and designs.
Learn about innovative sequencing library preparation methods to suit any need.
Library prep and array kit selector tool
Find the right sequencing library preparation kit or microarray for your application.
Find the right sequencing platform to fit your needs, from benchtop to production-scale sequencers.
Compare array scanning systems for rapid, sensitive, and accurate genetic analysis results.
See how Illumina software products can offer solutions for any workflow.
Explore features and benefits of BaseSpace Sequence Hub, a direct extension of your Illumina instruments.
Transform data into insights accurately and efficiently with Illumina DRAGEN secondary analysis.
Learn about NGS and see the benefits that this revolutionary technology can bring to your lab! Starting from the basics of NGS to workflows, tutorials, planning and more, see how to get started today.
Innovative Illumina sequencing platforms deliver exceptional data quality and accuracy at a massive scale. View benchtop and production-scale sequencer comparison tables.
Cancer research feature articles
Read featured articles from cancer research.
Illumina oncology research workflows
Download this flyer to learn more about scalable oncology research workflows with the NextSeq 2000 System.
Interested in learning more about cancer research?
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