Abstract
The advent of next-generation sequencing has made possible genome analysis at previously unattainable depth. Roche, Illumina and Life Technologies, among others, have developed well-established platforms for deep sequencing. Regardless of the instrument, one of the bottlenecks for next-generation sequencing is the amount of time and resources required for template and library preparation. Here we describe Epicentre’s Nextera™ technology (covered by issued and/or pending patents), which counters this bottleneck and simplifies the sample preparation procedure.
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CITATION STYLE
Syed, F., Grunenwald, H., & Caruccio, N. (2009). Next-generation sequencing library preparation: simultaneous fragmentation and tagging using in vitro transposition. Nature Methods, 6(11), i–ii. https://doi.org/10.1038/nmeth.f.272
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