Small RNA NGS Sequencing Service, Single Adapter Ligation and Circularization-basedRealSeq® Technology for small RNA sequencing library preparation
Library preparation and sequencing services for RNAs, miRNAs and other small RNAs from total RNA (tissue or cell culture) or from biofluid samples.
• Novel method for bias-free small-RNA sequencing libraries
• Superior quality sequencing libraries
• Avoids underdetection of many miRNAs
• For total RNA samples and biological samples (tissue and cells or biofluids)
• Service includes:
>> Preparation of small RNA sequencing libraries
>> Library QC
>> Next-Generation-Sequencing on an Illumina platform (MiniSeq or Next Seq)
>> Optional RNA Preparation without additional cost
Accuracy through circularization
RealSeq® is a novel method for preparing small-RNA sequencing libraries that nearly eliminates incorporation bias in Next-Generation-Sequencing (NSG). This technology solves the problem of commonly used sequencing library preparations that lead to underdetection of many miRNAs, some by as much as 10,000-fold.
Under-representation in sequencing libraries can obscure the presence of some RNAs, including potential biomarkers. Accurate quantification of microRNAs (miRNA) and other small RNAs is important for understanding their biology and for developing new biomarkers and therapeutic targets.
Most bias stems from sequence-dependent variability in the enzymatic ligation reactions that attach the two adapters to the 3’ and 5’ ends of the miRNAs /small RNAs during preparation of sequencing libraries. By using a novel single adapter and circularization, RealSeq® greatly reduces library preparation bias.
Read more about SomaGenics´ RealSeq® Technology:
Genome Biology 19:105 (2018)
Decreasing miRNA sequencing bias using a single adapter and circularization approach. Sergio Barberán-Soler, Jenny M. Vo, Ryan E. Hogans, Anne Dallas, Brian H. Johnston and Sergei A. Kazakov.
RealSeq® Technology Overview
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.
RealSeq® accurately quantifies small RNAs
One pmole of miRXPlore Universal Reference pool (Miltenyi Biotec) was used to compare incorporation bias in six different 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. Libraries prepared using RealSeq®-AC have substantially fewer miRNAs with bias than the ones prepared using any of five other commercially available library preparation kits.
Libraries prepared with RealSeq®-biofluids yield substantially more miRNAs compared to competitor kits
Sequencing results obtained from commercially available library preparation kits were compared using 200-ul aliquots from the same plasma samples. Short reads are classified as reads <15 nt length after adapter trimming. Reads passing this filter are then aligned to a reference file with all human miRNAs (miRBase 21, orange), and the remaining reads are aligned to the human genome (hg19, red).
RealSeq® - biofluids yields significantly fewer short or unmappable reads (grey) than the other two commercial libraries available that are indicated for biofluids analysis.
The number of sequenced miRNAs and of other mappable small RNAs is substantially higher.
RealSeq®-biofluids allows sequencing of significantly more miRNAs
Comparison of miRNAs read frequencies of three different library preparation kits (gel-free protocols) from 200 ul plasma samples. Reads were subsampled to 10 million reads per kit and aligned to a reference that includes all human miRNAs listed in miRBase 21 (Miltenyi Biotec). The number of miRNAs detected at different coverage for each library preparation kit is shown.
Especially low copy-number miRNAs are significantly more sequenced when the RealSeq® - biofluids kit was used for library preparation.
|Small RNA LibraryPrep-Sequencing-Service (from Cell/Tissue Sample or total RNA) with RealSeq-AC||500-totalRNA-SOM||10 Mio reads/sample||365 €||DETAILS||Add to Cart|
|Small RNA LibraryPrep-Sequencing-Service (from Biofluid Sample or total RNA from Biofluids) with RealSeq-biofluids||600-totalRNA-SOM||10 Mio reads/sample||365 €||DETAILS||Add to Cart|