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Discover the Features and Benefits of “True Multiplexing”
seqWell’s integrated normalizing library prep technology allows the creation of balanced library pools without the need for sample or library normalization. Our fast, simplified workflows multiplex 100’s to 1000’s of samples for loading on a single sequencing run enabling enhanced overall sequencing performance.
Simple & Fast
Multiplex 1000’s of samples with ease using our kits.
Built-in normalization with every kit.
Uniform insert sizes & sample read counts.
Improved overall sequencing performance
Simple Three Step Protocol:
Our NGS workflows utilize a transposase to selectively tag DNA samples in a unique sequential manner. The sequential tagging process provides more control of each step versus other transposon methods and less prone to bias and input DNA variations.
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