当社のがんパネル製品
イルミナのAmpliSeqと当社のTruSightがんパネルは、がん研究向けに数種のライブラリー調製、シーケンス、およびデータ解析オプションを提供しています。効率化されたライブラリー調製ワークフローおよび柔軟なキット構成により、複数の研究デザインに対応します。イルミナのシステムは業界屈指のシーケンスを提供します。実際、世界のシーケンスデータの90%以上はイルミナの sequencing by synthesis（SBS）ケミストリーを使用して生成されています。
貴社のアプリケーション分野を選択して、当社のがん研究製品の詳細をご覧ください。
ライブラリー調製
TruSight Oncology 500
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
TruSight Tumor 170
Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample.
TruSight Oncology UMI Reagents
The TruSight Oncology UMI Reagents and UMI Error Correction App reduce error rates in samples to ≤0.007%, enabling the detection of low frequency variants.
AmpliSeq for Illumina Focus Panel
Targeted DNA and RNA panel investigating 52 genes with known relevance to solid tumors.
AmpliSeq for Illumina Comprehensive Panel v3
Targeted DNA and RNA panel investigating variants across 161 genes associated with a range of cancer types.
TruSight Tumor 15
Focused sequencing panel to assess 15 genes that are commonly mutated in solid tumors in a single assay, with a simple, rapid workflow.
TruSight RNA Fusion
Provides comprehensive gene fusion detection in formalin-fixed, paraffin-embedded (FFPE) and other cancer research samples.
AmpliSeq for Illumina Cancer Hotspot Panel v2
Targeted panel investigating hotspot regions of 50 genes with known associations to cancer.
AmpliSeq for Illumina Comprehensive Cancer Panel
Targeted panel investigating the exonic regions of 409 genes with known associations to cancer.
AmpliSeq for Illumina Custom Panel
Targeted custom panel optimized for specific targets or genomic content of interest.
シーケンス
MiSeq System
Desktop sequencer featuring a simple NGS workflow, integrated data analysis software, and unmatched accuracy.
MiSeqDx System in Research Mode
FDA-cleared in vitro diagnostic NGS system that also operates in research mode to generate accurate, reliable data.
MiniSeq System
Simple, affordable solution for low-throughput targeted cancer sequencing.
NextSeq 550 System
Sequencing and cytogenomic array scanning on a single system, with a seamless transition between applications.
NextSeq 550Dx System in Research Mode
FDA regulated, CE-IVD, next-generation sequencing system that also runs in research mode to enable high-throughput clinical research.
iSeq 100 System
Affordable, fast, and accessible sequencing power for targeted or small genome sequencing in any lab.
データの解析および保管
Local Run Manager
Easy-to-use software for automated on-instrument data analysis.
BaseSpace Sequence Hub
The Illumina genomics computing environment for NGS data analysis and management.
VariantStudio Software
A powerful analysis and reporting tool that provides biological insight into genomic variant data.
ライブラリー調製
TruSight Myeloid
The TruSight Myeloid Sequencing Panel targets variants associated with myeloid malignancies such as AML, MDS, MPN, CML, CMML, and JMML.
AmpliSeq for Illumina Myeloid
Targeted panel to investigate 40 DNA genes, 29 RNA fusion driver genes, and 5 gene expression levels associated with myeloid cancers.
TruSight Oncology UMI Reagents
The TruSight Oncology UMI Reagents and UMI Error Correction App reduce error rates in samples to ≤0.007%, enabling the detection of low frequency variants.
TruSight RNA Fusion
Provides comprehensive gene fusion detection in formalin-fixed, paraffin-embedded (FFPE) and other cancer research samples.
AmpliSeq for Illumina Custom Panel
Targeted custom panel optimized for specific targets or genomic content of interest.
シーケンス
MiSeq System
Desktop sequencer featuring a simple NGS workflow, integrated data analysis software, and unmatched accuracy.
MiSeqDx System in Research Mode
FDA-cleared in vitro diagnostic NGS system that also operates in research mode to generate accurate, reliable data.
MiniSeq System
Simple, affordable solution for low-throughput targeted cancer sequencing.
NextSeq 550 System
Sequencing and cytogenomic array scanning on a single system, with a seamless transition between applications.
NextSeq 550Dx System in Research Mode
FDA regulated, CE-IVD, next-generation sequencing system that also runs in research mode to enable high-throughput clinical research.
iSeq 100 System
Affordable, fast, and accessible sequencing power for targeted or small genome sequencing in any lab.
データの解析および保管
Local Run Manager
Easy-to-use software for automated on-instrument data analysis.
BaseSpace Sequence Hub
The Illumina genomics computing environment for NGS data analysis and management.
VariantStudio Software
A powerful analysis and reporting tool that provides biological insight into genomic variant data.
ライブラリー調製
TruSight Cancer
This expert-defined sequencing panel targets 94 genes and 284 SNPs associated with a predisposition towards various cancers.
AmpliSeq for Illumina BRCA Panel
Targeted panel investigating somatic and germline variants in BRCA1 and BRCA2.
AmpliSeq for Illumina Custom Panel
Targeted custom panel optimized for specific targets or genomic content of interest.
シーケンス
MiSeq System
Desktop sequencer featuring a simple NGS workflow, integrated data analysis software, and unmatched accuracy.
MiSeqDx System in Research Mode
FDA-cleared in vitro diagnostic NGS system that also operates in research mode to generate accurate, reliable data.
MiniSeq System
Simple, affordable solution for low-throughput targeted cancer sequencing.
NextSeq 550 System
Sequencing and cytogenomic array scanning on a single system, with a seamless transition between applications.
NextSeq 550Dx System in Research Mode
FDA regulated, CE-IVD, next-generation sequencing system that also runs in research mode to enable high-throughput clinical research.
iSeq 100 System
Affordable, fast, and accessible sequencing power for targeted or small genome sequencing in any lab.
データの解析および保管
Local Run Manager
Easy-to-use software for automated on-instrument data analysis.
BaseSpace Sequence Hub
The Illumina genomics computing environment for NGS data analysis and management.
VariantStudio Software
A powerful analysis and reporting tool that provides biological insight into genomic variant data.
ライブラリー調製
TruSight RNA Pan-Cancer
Targeting 1385 cancer genes for gene expression, variant, and fusion detection studies in many RNA sample types including blood, bone marrow, and formalin-fixed, paraffin-embedded (FFPE) tissue.
TruSight Oncology UMI Reagents
The TruSight Oncology UMI Reagents and UMI Error Correction App reduce error rates in samples to ≤0.007%, enabling the detection of low frequency variants.
TruSight RNA Fusion
Provides comprehensive gene fusion detection in formalin-fixed, paraffin-embedded (FFPE) and other cancer research samples.
AmpliSeq for Illumina Cancer Hotspot Panel v2
Targeted panel investigating hotspot regions of 50 genes with known associations to cancer.
AmpliSeq for Illumina Comprehensive Cancer Panel
Targeted panel investigating the exonic regions of 409 genes with known associations to cancer.
シーケンス
MiSeq System
Desktop sequencer featuring a simple NGS workflow, integrated data analysis software, and unmatched accuracy.
MiSeqDx System in Research Mode
FDA-cleared in vitro diagnostic NGS system that also operates in research mode to generate accurate, reliable data.
MiniSeq System
Simple, affordable solution for low-throughput targeted cancer sequencing.
NextSeq 550 System
Sequencing and cytogenomic array scanning on a single system, with a seamless transition between applications.
NextSeq 550Dx System in Research Mode
FDA regulated, CE-IVD, next-generation sequencing system that also runs in research mode to enable high-throughput clinical research.
iSeq 100 System
Affordable, fast, and accessible sequencing power for targeted or small genome sequencing in any lab.
データの解析および保管
Local Run Manager
Easy-to-use software for automated on-instrument data analysis.
BaseSpace Sequence Hub
The Illumina genomics computing environment for NGS data analysis and management.
VariantStudio Software
A powerful analysis and reporting tool that provides biological insight into genomic variant data.
ライブラリー調製
AmpliSeq for Illumina Immune Response Panel
Targeted RNA expression panel investigating 395 genes involved in tumor-immune system interactions.
AmpliSeq for Illumina Custom Panel
Targeted custom panel optimized for specific targets or genomic content of interest.
シーケンス
MiSeq System
Desktop sequencer featuring a simple NGS workflow, integrated data analysis software, and unmatched accuracy.
MiSeqDx System in Research Mode
FDA-cleared in vitro diagnostic NGS system that also operates in research mode to generate accurate, reliable data.
MiniSeq System
Simple, affordable solution for low-throughput targeted cancer sequencing.
NextSeq 550 System
Sequencing and cytogenomic array scanning on a single system, with a seamless transition between applications.
NextSeq 550Dx System in Research Mode
FDA regulated, CE-IVD, next-generation sequencing system that also runs in research mode to enable high-throughput clinical research.
iSeq 100 System
Affordable, fast, and accessible sequencing power for targeted or small genome sequencing in any lab.
データの解析および保管
Local Run Manager
Easy-to-use software for automated on-instrument data analysis.
BaseSpace Sequence Hub
The Illumina genomics computing environment for NGS data analysis and management.
VariantStudio Software
A powerful analysis and reporting tool that provides biological insight into genomic variant data.
ライブラリー調製
TruSight RNA Pan-Cancer
Targeting 1385 cancer genes for gene expression, variant, and fusion detection studies in many RNA sample types including blood, bone marrow, and formalin-fixed, paraffin-embedded (FFPE) tissue.
AmpliSeq for Illumina Custom Panel
Targeted custom panel optimized for specific targets or genomic content of interest.
シーケンス
MiSeq System
Desktop sequencer featuring a simple NGS workflow, integrated data analysis software, and unmatched accuracy.
MiSeqDx System in Research Mode
FDA-cleared in vitro diagnostic NGS system that also operates in research mode to generate accurate, reliable data.
MiniSeq System
Simple, affordable solution for low-throughput targeted cancer sequencing.
NextSeq 550 System
Sequencing and cytogenomic array scanning on a single system, with a seamless transition between applications.
NextSeq 550Dx System in Research Mode
FDA regulated, CE-IVD, next-generation sequencing system that also runs in research mode to enable high-throughput clinical research.
iSeq 100 System
Affordable, fast, and accessible sequencing power for targeted or small genome sequencing in any lab.
データの解析および保管
Local Run Manager
Easy-to-use software for automated on-instrument data analysis.
BaseSpace Sequence Hub
The Illumina genomics computing environment for NGS data analysis and management.
VariantStudio Software
A powerful analysis and reporting tool that provides biological insight into genomic variant data.
包括的ゲノムプロファイリング(CGP)
このNGSアプローチは、さまざまなバリアントタイプを含む数百ものがん関連マーカーを、1回のアッセイで解析します。その効果や他の一般的ながんNGS手法との比較などを探ります。
Recent Developments in Cancer Research
The Spatial Multiomics Revolution
NanoString Technologies and Illumina to discuss benefits of whole transcriptome spatial analyses at AGBT
記事を読む
Whole Genome Sequencing Gives Scientists a Detailed Map of Cancer Mutations
Dr. Serena Nik-Zainal, a clinical geneticist, and her team at the University of Cambridge are studying how cancer genome profiling could help clinicians better fight the malignancies.
インタビューを読む
Patient Success Story: Beating Stage IV Lung Cancer
AJ Patel had six months to live. Eight years later, he tells us how biomarker testing changed everything.
記事を読む補足資料
がんのベールを取る：TruSight Tumor 170
新しいエンリッチメントベースのがん研究アッセイは、DNAとRNAの両方から、Small variant、遺伝子増幅、融合遺伝子とスプライスバリアントを検出することができます。
Interested in receiving newsletters, case studies, and information on cancer genomics?
サインアップ
Cancer Panels Demonstrate Value in Tumor Studies
Clinical researchers share how TruSight Tumor 170 and TruSight Oncology 500 can play an important role in tumor characterization.
参考文献
* 社内計算データにより。Illumina, Inc. 2015.