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Spike-in-RNA

Spike-in RNA Variant Control Mixes

Company:

The Only RNA Control designed for Splice
Variant Detection Consist of

  • transcript variants representing
  • Alternative splicing
  • Promoter and poly(A) site usage
  • Overlapping genes
  • Antisense transcription

Product Description

Spike-in controls are essential in RNA-Seq experiments to assess workflow and platform properties. However, existing external RNA controls are generally mono-exonic and non-variant, significantly limiting their ability to reflect the true nature of eukaryotic transcriptomes. These are characterized by extensive splicing, alternative and antisense transcription, overlapping genes, and rare events like the formation of fusion genes. The performance of RNA preparation, library generation, sequencing, and bioinformatics algorithms can furthermore not be assessed adequately without known transcript spike-in controls of representative complexity.
To address this gap, Lexogen has conceived Spike-In RNA Variants (SIRVs) for the quantification of mRNA isoforms in Next Generation Sequencing (NGS). The SIRVs are a set of 69 artificial transcript variants which mimic 7 human model genes. They are complemented by additional isoforms to comprehensively reflect variations of alternative splicing, alternative transcription start- and end-sites, overlapping genes, and antisense transcripts. The accuracy of mapping, isoform assembly and quantification can be assessed, making isoform-quantification based experiments comparable.

Validate your RNA-Seq quantification pipeline and its annotation-robustness

The a priori knowledge of SIRV transcript sequences and concentrations allows to assess the isoform-specific performance of an RNA-Seq experiment. In addition to the correct annotation of the SIRVs, one insufficient and one over-annotation are supplied to enable the testing of NGS data evaluation algorithms for their robustness towards “real life”, imperfect annotations

3 SIRV mixes for differential expression

The SIRVs are provided as a set of 3 SIRV mixes, E0, E1, and E2, with each mix containing all 69 SIRVs but in different concentration ratios. E0 contains the RNAs in equimolar ratio, E1 covers one order of magnitude (up to 1:8) and in E2 SIRV concentration range over more than two orders of magnitude (up to 1:128). The comparison of samples spiked with these different mixes enables the quantitative assessment of differential expression workflows on the transcript level.

Product Composition

The SIRVs are provided as three mixtures containing the 69 transcripts of the 7 SIRV genes in different concentrations.