Discover the Features and Benefits of “True Multiplexing”
plexWell’s integrated normalizing library prep technology allows the creation of balanced library pools without the need for sample or library normalization. The simplified 3-hour workflow multiplexes 100's to 1000's of samples for loading on a single sequencing run enabling enhanced overall sequencing performance.
• Multiplex 100’s to 1000’s of Samples in a Single Sequencing Run
• Eliminate Time-Consuming Input and Library Quant
• Uniform Depth of Coverage and Insert Size on All Samples
• No Upfront or Additional Equipment Needed
plexWell Achieves a Significantly Better Level of Multiplexing Uniformity for Highly Multiplex Sequencing Applications
At left, sequencing results obtained for sequencing 192 samples of amplified single-cell cDNA with plexWell (blue) and For Nextera™ reagents (gray). Input DNA was pre-normalized, whereas plexWell library was made from un-normalized amplified cDNA. Read count variation for plexWell showed 27% CV versus 71% CV for Nextera.
plexWell technology yields balanced multiplexed libraries containing highly uniform insert size distributions and samples read counts
plexWell Delivers Minimal Bias for Diverse Applications