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Today’s genomic solutions for tomorrow’s cancer breakthroughs

Cancer Genomics Research

Illumina next-generation sequencing (NGS) and microarray technologies represent the gold standard in quality worldwide—and account for ~90% of the world’s sequencing data.* Innovative, intuitive, and completely integrated, our sample-to-data solutions empower your lab to keep ahead of the curve in the rapidly evolving genomics revolution. So you’ll be better able to perform the world-class cancer genomics research you strive for—with the goal of uncovering new insights into the biology of cancer that can lead to meaningful advances in personalized medicine.

Our comprehensive genomics product offerings support multiple cancer research applications, including studies of DNA, RNA, epigenetics, and more. Our range of sequencers can be scaled to meet your needs—from powerful, yet personal, benchtop models to versatile, high-throughput systems. With intuitive data analysis and management capabilities and unsurpassed customer support, we can deliver the answers you seek—quickly, accurately, and cost-effectively.

Oncology

During this webinar, our expert speakers provide background information on next-generation sequencing (NGS), discuss the achievements and challenges associated with NGS, and discuss how an integrated multiomics approach can be used in cancer diagnosis and treatment.

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Redefining NGS in Cancer Research
空間マルチオミクス革命
空間マルチオミクス革命

NanoString Technologiesとイルミナが、AGBTにおける全トランスクリプトーム空間解析の利点について議論

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FMRIはイルミナの新しいエクソーム濃縮を用いてゲノム研究の効率向上を実現しています
FMRIはイルミナの新しいエクソーム濃縮を用いてゲノム研究の効率向上を実現しています

Future Medicine Research InstituteのChief ResearcherであるSookyoung Kim氏がIllumina DNA Prep with Exome 2.0 Plus Enrichmentの評価結果について語ります。

インタビューを読む
患者の成功事例:ステージIVの肺がんに打ち勝つ
患者の成功事例:ステージIVの肺がんに打ち勝つ

AJ Patelは6カ月生存しました。8年後、彼はバイオマーカー検査がいかにすべてを変革したかを語っています。

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The NovaSeq 6000 System

High-quality, high-coverage sequencing offers a comprehensive view of the genome to detect variants accurately, characterize isoforms, and more. With increased throughput and reduced price per sample, the NovaSeq 6000 System is ideal for data-intensive applications.

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The NovaSeq 6000 System
AmpliSeq for Illumina Focus Panel

Targeted DNA and RNA research panel investigating 52 genes with known relevance to solid tumors.

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NextSeq 550 System

Flexible desktop sequencing system that supports various applications, from targeted panels to whole-genome sequencing.

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BaseSpace Sequence Hub

The Illumina genomics computing environment for NGS data analysis and management, so labs can analyze, archive, and share data easily.

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10X Genomics Chromium Single Cell Multiome ATAC + Gene Expression

Unify single-cell gene expression and chromatin accessibility to help reveal cellular mechanisms driving gene regulation.

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Measure Protein Expression with RNA-Seq

Learn how to incorporate protein detection into bulk RNA-Seq and develop a workflow for BEN-Seq, providing a holistic approach to cell analysis.

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NGS technology has accelerated the discovery of variants associated with cancer. Some of these research discoveries became the basis for companion diagnostics and laboratory developed tests (LDT) now in use in molecular diagnostic laboratories worldwide. We spoke with key opinion leaders about the ongoing challenges and potential of NGS in oncology testing.

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The Changing Landscape of NGS Implementation in Molecular Diagnostic Laboratories
NGSのビギナーガイド

次世代シーケンスの基礎知識を学び、始めるためのヒントが得られます

詳細はこちら
NGSのビギナーガイド
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Cancer Research Review

An overview of recent cancer genomics research publications featuring Illumina technology.

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Insights into Leukemia and Lymphoma

Munich Leukemia Laboratory is using NGS to gain a better understanding of leukemia and lymphoma subtypes and discover new therapeutic pathways.

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Interested in receiving newsletters, case studies, and information on cancer genomics?
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Cancer Research Webinar
Educational Webinars

Explore a variety of webinars on topics ranging from cancer research to NGS data analysis, microbiome studies, and more.

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Cancer Research Webinar
2021 Cancer Research Methods Guide

This updated guide provides an overview of NGS-based and microarray workflows for a broad range of cancer research applications.

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Sequencing Analysis of Tissue Samples: Fresh Frozen vs. FFPE

A researcher from Massachusetts General Hospital compares sequencing results from FFPE and fresh-frozen tumor samples.

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References

*Data on file based on a 2013 study.