Solutions for NGS Library Preparation Workflow
Thermo Scientific NGS library preparation, cleanup and size-selection products combine all necessary NGS library construction steps into one streamlined user-friendly workflow. Optimized for maximal performance and flexibility Thermo Scientific reagents allow for fast, effortless and reliable DNA library construction from minimal DNA sample input.
The Thermo Scientific product portfolio provides two distinct NGS library construction technologies – ClaSeek and MuSeek – each created to meet researcher's most demanding needs. The unmatched versatility of ClaSeek kits and incredible ease of use of MuSeek kits enables scientists to achieve excellent results with less effort and more time saved.
|Sample input||5 ng-1 µg physically sheared DNA||100 ng of intact genomic DNA, cDNA|
|PCR-free protocol available||Yes||No|
|Physical sample fragmentation required||Yes||No (transposon-mediated)|
|Protocol||<60 min PCR-free protocol
~120 min amplification protocol
|<80 min total time|
|NGS platform compatibility
||Illumina MiSeq©, HiSeq, Ion Torrent PGM©, Ion Proton©
||Ion Torrent PGM©, Ion Proton©, Illumina MiSeq™ Illumina HiSeq™|
Thermo Scientific ClaSeek Library Preparation Kits are designed for fast, convenient and accurate DNA library construction from DNA sample input as low as 5 ng. Available amplification-free protocols eliminate any possible PCR-related bias, resulting in uniform data coverage and reliable sequencing results.
- PCR-free–significantly minimized bias and improved data coverage with amplification-free protocol
- Flexible–library construction from 5 ng to 1 µg DNA sample
- Fast and convenient–up to 50% shorter library preparation workflow with significantly less hands-on time
Ligation-based sequencing adapter addition method
The Thermo Scientific ClaSeek™ library preparation technology utilizes a ligation-based sequencing adapter addition method. During initial steps fragmented genomic DNA sample is end-converted by blunting 5′- and 3′-overhangs and phosporylation of 5′-ends of fragmented DNA. Depending on the sequencing platform, a single dA-overhang may be added to the 3′-end of each strand. In the following step sequencing instrument-specific adapters are ligated to each end of converted DNA fragments. Subsequent MagJET cleanup and size-selection steps allow for selection of a sequencing-ready DNA library within the desired read-length interval. Alternatively an additional high-fidelity amplification step is available for DNA library construction from DNA sample amounts as little as 5 ng.
Optimized end conversion and adapter addition master mixes
ClaSeek Library Preparation kits provide optimized End conversion and Adapter Addition master mixes allowing for fast and convenient PCR-free DNA library construction in less than one hour with less pipetting steps and reduced hands-on time. Optional amplification protocols allow for library preparation using ultra-low (5 ng) DNA sample input.
Speed and convenience
Thermo Scientific MuSeek library preparation kits utilize an innovative transposon-based technology that allows enzymatic fragmentation and simultaneous tagging of the target DNA, eliminating the need for physical shearing, DNA end-repair, and adapter ligation steps. This enables fast library construction with minimal hands-on time and less effort.
- Fast–library generation in less than 80 minutes
- Easy-to-use–no physical shearing, end-repair and ligation steps
- Universal–one protocol for generating different fragment length libraries
Enzymatic fragmentation and simultaneous tagging
MuSeek Library Preparation Kits utilize an innovative transposon-based technology that allows enzymatic fragmentation and simultaneous tagging of the target DNA, eliminating the need for physical sample shearing, DNA end-repair, and adaptor ligation steps.
The fragmentation and tagging reaction is catalyzed by a homotetrameric MuA transposase complex (75 kDa protein originating from bacteriophage Mu) containing two 50 bp double-stranded transposon DNA ends with a specific MuA binding sequence. Initially, the genomic DNA sample is simultaneously fragmented and tagged with transposon sequences at each end of resulting DNA fragments (1). In the next step the 3'-ends of the fragmented DNA are elongated over the 5 nt gaps generated during the transposition reaction and further extended into transposon sequences (2) . Sequencing platform-specific adaptors are added to the fragments in a subsequent PCR-based adaptor-addition reaction. In the initial cycles of PCR the first 16 nt of the adaptor 3'-ends hybridize to transposon sequences in tagged DNA fragments (2). In later PCR cycles the fragments are amplified using a pair of external primers.
Reliable NGS Library Cleanup and Size Selection
Thermo Scientific MagJET and GeneJET NGS Cleanup and Size Selection kits are optimized for robust and efficient DNA fragment library purification and size selection from a large variety of enzymatic reaction mixtures used in NGS workflows.
- Robust–reliable cleanup and size selection from different reaction mixtures and buffers
- Flexible–user-defined size-selection of exact DNA fragment range
- NGS-grade purity–complete removal of NGS adapters, primers, nucleotides, enzymes and other reaction components inhibiting NGS workflow
- High-throughput compatible–easy to automate on Thermo Scientific KingFisher magnetic particle processors for high-throughput sample handling
Robust cleanup and size selection
Fragmented E. coli genomic DNA (1 µg) samples, each spiked in different reaction mixtures and buffers (a-h) typical for next-generation sequencing workflow, were size selected using MagJET and other supplier protocols. Isolated fragment libraries were analyzed on an agarose gel. Expected size selection peak areas are marked with a dotted line.
a – End Conversion Reaction mixture, IT;
b – PCR Reaction mixture (1);
c – PCR Reaction mixture (2);
d – Ligation Mixture;
e – End Conversion Reaction mixture (IL);
f – Fragmentation reaction buffer;
g – Elution buffer;
h – Nebulization buffer;
C – Control (input DNA)
Efficient size selection of different fragment lengths
Fragmented E. coli genomic DNA samples were end-converted, followed by Illumina- (A) or Ion Torrent- (B) compatible adapter addition using recommended Thermo Scientific ClaSeek protocols. Different DNA fragment ranges were size-selected corresponding to relevant sequencing read lengths. Size selection was preformed using MagJET NGS Cleanup and Size Selection Kit. DNA library samples were analyzed on Bioanalyzer 2100 (Agilent Technologies, Inc.).
For Research Use Only. Not for use in diagnostic procedures.