TruSeq RNA Exome
Provides a reproducible, economical solution for sequencing RNA from FFPE tissues and other low-quality samples. Accuracy from as little as 10 ng total RNA.Read More...
Achieve exceptionally rapid targeted RNA enrichment with the new Illumina RNA Prep with Enrichment. Use code RNA25 at checkout to receive 25% off your first order, now through the end of 2020.*
*Offer valid for library prep kit only. Index adapters and panels are not included in this promotion.
TruSeq RNA Exome, previously known as the TruSeq RNA Access Library Prep Kit, converts total RNA into template molecules of known strand origin, followed by sequence-specific capture of coding RNA. This provides a low-cost solution for analyzing human RNA isolated from formalin-fixed, paraffin-embedded (FFPE) tissues and other low-quality samples.
TruSeq RNA Exome generates RNA sequencing (RNA-Seq) libraries from degraded samples that focus on the RNA coding regions. Isolating these high-value content regions to help maximize discovery power, while requiring only a fraction of the read depth of total RNA sequencing. The results are low input requirements, high sample throughput, and cost-effective transcriptome analysis. Reagent volumes supplied are sufficient to support 1- to 4-plex enrichment reactions.
Find automation vendors with robotic systems compatible with this product
Read a comprehensive assessment of Illumina’s ribosomal RNA depletion protocol
| 仪器 | 推荐的样本数 | 读长 |
|---|---|---|
| NextSeq 550 System | 5 to 16 samples per run (based on 25 million reads per sample) | 2 x 75 bp |
| HiSeq 2500 System | 24-160 samples per run (dual flow cell; based on 25 million reads per sample) | 2 x 75 bp |
| NovaSeq 6000 System | Samples per run (dual flow cell): S1: 96, S2: 96, S4: 192 (currently limited by available index combinations) | 2 × 100 bp |
| TruSeq RNA Exome | Illumina RNA Prep with Enrichment | Illumina Stranded mRNA Prep | |
|---|---|---|---|
| Assay Time | 约两天 | ||
| Automation Capability | 液体处理机器人 | 液体处理机器人 | 液体处理机器人 |
| Content Specifications | 捕获编码转录组/RNA外显子组 | ||
| Description | 为研究人员提供清晰、全面的编码转录组视图，链信息精确且样本起始量低。 | ||
| Hands-On Time | 约11小时 | ||
| Input Quantity | 10 ng新鲜/冷冻样本来源的总RNA，或20 ng FFPE样本来源的总RNA | ||
| Mechanism of Action | 以编码RNA为靶标的生物素化的捕获探针。不要求RNA带有poly-A尾巴。 | ||
| Method | Exome Sequencing , mRNA Sequencing | mRNA Sequencing , 靶向RNA测序 , 靶向富集 | mRNA Sequencing |
| Multiplexing | 多达24个单标签、96个组合（CD）双标签 | ||
| Specialized Sample Types | FFPE Tissue, Low-Input Samples | Blood, FFPE Tissue, Low-Input Samples | Low-Input Samples, Not FFPE-Compatible |
| Species Category | 人类 | Virus, 人类 | Bovine, Mammalian, Mouse, Rat, 人类 |
| Strand Specificity | Stranded | Non-Stranded | Stranded |
The product previously known as the TruSeq RNA Access Library Prep Kit (Cat. No. RS-301-2001 and RS-301-2002) is now called TruSeq RNA Exome. The product configuration has changed. In the new configuration, major components such as library preparation, index adapters, enrichment reagents, and exome panels can be purchased separately. If you were previously buying Cat. No. RS-301-2001 or Cat. No. RS-301-2002, purchase the following components: TruSeq RNA Library Prep for Enrichment (Cat. No. 20020189), TruSeq RNA Enrichment (Cat. No. 20020490), Exome Panel (Cat. No. 20020183), and one item from the Index Adapters section below.
TruSeq RNA Exome enables detection of expressed fusion transcripts without the need to design probes specific for the fusion junction. The well-characterized BCR-ABL fusion is detected efficiently in the Universal Human Reference RNA (UHRR) sample at 25 M reads.
Evaluating RNA Quality from FFPE Samples
Technical Note | PDF1 MB
Robust low-input RNA sequencing with TruSeq Stranded Total RNA Library Prep Gold
Application Note | HTML
RNA-Seq Offers Significant Advantages in Immuno-Oncology Research
White Paper | PDF2 MB
Data Sheet | PDF | 5 versions
TruSeq RNA Exome Reference Guide Documentation
TruSeq RNA Exome Documentation
TruSeq RNA Exome Consumables & Equipment Documentation
TruSeq RNA Exome Checklist Documentation
自定义协议选择器
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A simple, scalable, cost-effective, rapid single-day solution for analyzing the coding transcriptome leveraging as little as 25 ng input of standard (non-degraded) RNA.
Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information.
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