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RNA Sequencing
(noun) /RNA ˈsiːkwənsɪŋ/
Whole-transcriptome analysis with RNA sequencing (RNA-Seq) is at the cutting edge of NGS capabilities and allows to determine RNA molecules in a sample at the moment of sampling. The transcriptome is a highly dynamic cellular feature that opens up a world of discovery potential. Changes in response to drugs, various states of disease, post-transcriptional modifications, and alternatively spliced transcripts are just some examples of discoveries made possible by RNA-Seq.
RNA-Seq Applications
RNA-Seq is used to measure gene and transcript abundance levels, and to assess qualitative information of the transcriptome of all species. It is commonly used to:
- perform differential expression analysis,
- identify and quantify transcript isoforms,
- perform alternative splicing studies,
- assess long non-coding RNAs,
- detect transcript variants (including SNPs and SNVs),
- study fusion transcripts,
- (re-)annotate model and non-model organisms,
- perform transcriptomics on archived biobank samples (FFPE material)
CORALL RNA-Seq Library Prep Kits
The CORALL RNA-Seq Library Prep Kits enables fast and cost-efficient generation of stranded, UMI labelled, and unique dual indexed libraries for whole transcriptome analyses using Illumina® NGS platforms.
Watch a short video to learn more about CORALL:
Benefits
One for all and all-in-one. CORALL RNA-Seq is a well-established, fragmentation-free, and universal whole transcriptome RNA-Seq library prep which is completed in 6 steps (4.5 hours). CORALL is the universal solution for all your samples offering exceptional performance on low input samples, down to 1 ng starting amount. It is the ideal solution for total RNA-Seq analysis on degraded and FFPE samples.
New! Adjustable library size to perfectly fit your application: CORALL RNA-Seq V2 allows generation of longer libraries (~ 550 bp) for demanding applications such as alternative splicing, isoform analysis, and fusion detection.
Time saving
Excels with low input
Unlocks challenging samples
NEW! Adjustable size
Not sure which CORALL RNA-Seq product is right for you?
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NEW! CORALL RNA-Seq V2 Specifications
CORALL RNA-Seq V2 is a fast and flexible kit for whole transcriptome sequencing with a wide input range. CORALL RNA-Seq V2 is available as standalone kit, mRNA-Seq bundle including poly(A) selection and Total RNA-Seq bundle including RiboCop rRNA depletion (Table 1).
Table 1 | CORALL RNA-Seq V2 workflow specifications | ||||||||
---|---|---|---|---|---|---|---|---|
Feature | Specification | Benefit | ||||||
CORALL RNA-Seq V2 (stand-alone Kit) | CORALL mRNA-Seq V2 with Poly(A) Selection | CORALL Total RNA-Seq V2 with RiboCop | ||||||
Input RNA quantity | 0.1 ng – 100 ng | 1 ng – 1000 ng | 1 ng – 1000 ng | Supports the widest input range available on the market, delivers consistent library output over the full input range | ||||
RNA types | Total RNA | Poly(A) RNA | Ribo-depleted RNA | Supports all Whole Transcriptome RNA-Seq Applications | ||||
RNA quality | All qualities, including degraded RNA, FFPE | High-quality RNA (RIN > 8) | All qualities, including degraded RNA, FFPE | Supports all RNA qualities, high sensitivity and high-quality results for difficult material and FFPE samples | ||||
Workflow time* | 4.5 hours | 5.5 hours | 6 hours | Time-saving workflow with less steps, from sample to sequencing-ready library in one day | ||||
Kit reaction sizes | 24, 96, 384 | 96, 384 | 24, 96 | Scalable for evaluation, adoption and high-throughout applications | ||||
Technology | Fragmentation-free library prep using displacement-stop technology | Poly(A) selection by hybridization / capture and CORALL library prep | Hybridization / capture rRNA-depletion without enzymatic digestion and CORALL library prep | – Fragmentation-free workflow – No second strand synthesis – No adaptor titration, less adapter-dimers – Excellent inherent strandedness (> 99 %) | ||||
Unique Dual Indexing (UDI) | All CORALL RNA-Seq V2 Kits and Bundles contain 12 nt UDI Sets. | Maximized sequencing output on all instruments | ||||||
Unique Molecular Identifiers (UMIs) | All CORALL RNA-Seq V2 Kits and Bundles contain built-in UMIs. | Supports identification and removal of PCR duplicates for all sample types and quantities without additional purchases | ||||||
Automation Capability | All CORALL RNA-Seq V2 workflows can be automated on liquid handlers. | Supports high-throughput applications | ||||||
* Workflow time is based upon incubation times and expected times for hands-on-steps. Actual workflow time may vary. | ||||||||