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Developed in collaboration with cancer genomics experts, these predesigned, ready-to-use oligos enable researchers to sequence a variety of genes and single nucleotide polymorphisms (SNPs) previously linked to cancer predisposition.
TruSight Cancer includes genes associated with both common (e.g., breast, colorectal) and rare cancers. In addition, the set includes 284 SNPs found to correlate with cancer through genome-wide association studies (GWAS). Content selection was based on expert curation of the scientific literature and other high-quality resources.
The TruSight Cancer sequencing panel provides custom oligos targeting identified regions of interest. Sufficient product is supplied for four enrichment reactions. TruSight Cancer is compatible with TruSight Rapid Capture.
6 human reference samples were prepared using the TruSight Cancer sequencing panel. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 100 bp read length configuration with dual indexing. The total yield was 5.2 Gb with 95.8% of bases at or above Q30.
* Note that access to this data requires a BaseSpace Sequence Hub login.
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This product is available as an Illumina Advantage (TG) product. Illumina Advantage large-scale sequencing products feature lot-specific shipments and testing, extended shelf life, and advanced change notifications for greater laboratory efficiency.
| 装置 | 推奨サンプル数 | リード長 |
|---|---|---|
| MiniSeq System | Samples per run: mid output: 12, high output: 24 (based on > 20x coverage per target) | Up to 2 × 150 bp |
| MiSeq System | Samples per run (by reagent kit version): v2: 12, v3: 24 (based on > 20x coverage per target) | Up to 2 × 150 bp |
| NextSeq 550 System | Samples per run: mid output: 96, high output: 96 (based on > 20x coverage per target) | Up to 2 × 150 bp |
| TruSight Cancer | AmpliSeq for Illumina BRCA Panel | |
|---|---|---|
| Cancer Type | Pan-Cancer |
Researchers from the MGZ Medical Genetic Center are using the Infinium CytoSNP-850K BeadChip and the TruSight Cancer Panel to analyze chromosomal abnormalities.
Read MoreTruSight Rapid Capture Kit Documentation
カスタムプロトコルセレクタ
Generates customized, end-to-end instructions
小さなゲノム、PCRアンプリコン、プラスミド、またはcDNAのシーケンスライブラリーをわずか90分で調製し、DNAインプットの必要性を抑えます。
Targeted RNA research panel to investigate T cell diversity and clonal expansion by sequencing T cell receptor beta chain rearrangements.
Note regarding biomarker patents and other patents unique to specific uses of products:
Some genomic variants, including some nucleic acid sequences, and their use in specific applications may be protected by patents. Customers are advised to determine whether they are required to obtain licenses from the party that owns or controls such patents in order to use the product in customer's specific application.
