RealSeq-AC Kit for small RNA Library Construction from total RNA samples from tissue or cells (Illumina Platform)

Reducing Bias in Small-RNA Sequencing

Product Description

• Accurately quantifies biologically relevant  small RNAs
• Eliminates bias-induced over/under represented small RNAs
• Allows discovery of novel small RNAs
• Inputs between 1 ng to 100 ng of total RNA

Free bioinformatics service with the purchase of one library preparation kit until 31 March 2025

To receive a free basic bioinformatics service*, please mention promo code RSBANALYSIS when ordering this kit.

The basic bioinformatics service includes:

• Adapter trimming
• Sequence alignment to different reference databases relevant to your sample source
• Differential expression analysis

You receive an interactive HTML analysis report that summarizes the results from the analysis of your sequencing data, and the various generated CSV files from the analysis.

*Bioinformatics service has to be completed 6 months after ordering at the latest.

Workflow

3´ ends of miRNAs or any other 5’-p and 3’-OH small RNAs are ligated to RealSeq® adapters which contain standard adapter sequences (shown in blue and green) that are compatible with Illumina/Solexa sequencing.

Unligated adapters are blocked before circularization of the miRNA-adapter product and then removed. This intramolecular ligation is significantly more efficient than intermolecular ligation of 5’-adapters in standard two-adapter ligation schemes.

Reverse transcription of the circularized miRNA-adapter products yields monomer cDNAs with the targets sequences flanked by Illumina 5’- and 3’-adapter sequences. PCR amplification of the RT product with the extended, bar-coded PCR primers, yields amplicons ready for size selection using SPRI select technology (Beckman Coulter) which is included in RealSeq®-AC and RealSeq®-biofluids kits.

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Supporting Data

Reducing bias in small-RNA sequencing

Fig.1. One pmole of miRXPlore Universal Reference pool (Miltenyi Biotec) was used to compare incorporation bias in six different commercially available library preparation kits. Purified libraries were sequenced on the Illumina MiSeq platform. Trimmed sequencing reads were aligned to a custom miRNA reference. Reads mapping to miRNAs were counted and fold-deviations from the equimolar input were calculated and plotted as log2 values. Measurements of miRNA levels within a factor of two of the expected values (between vertical lines) are considered unbiased (Fuchs et al, 2015). The method of adapter attachment to the miRNAs is noted in the legend.

RealSeq®-AC is highly efficient, detecting more miRNAs in total RNA samples

Fig.2. RealSeq®-AC detects more miRNAs with over 5 or 10 reads per million, respectively, from total RNA samples compared to other kits for miRNA sequencing library preparation. RealSeq®-AC is optimized for inputs between 1 ng to 100 ng of total RNA. Lower numbers of PCR cycles are reducing PCR-induced issue.