Your next generation sequencing data is only as good as the library you create. Whether you need highly efficient DNA libraries for more uniform and deeper coverage or long span mate pair libraries to identify genome structural variation, gene/viral insertion sites or to create a scaffold for your de novo genome, the NxSeq® Technologies help you get there. Get more unique reads, deeper coverage, more complexity, and more efficiency from your fragment and mate pair library preps today.
NxSeq® UltraLow DNA Library Kit, 12 Reactions and Single Indexing Kits » Improve your whole genome coverage and uniformity with complex, Illumina-compatible DNA fragment libraries from as little as 50 pg of input DNA in about 3 hours.
NxSeq® AmpFREE Low DNA Library Kits and Adaptors (Illumina-compatible) » Highly efficient, complex DNA fragment libraries from only 75 ng of DNA in about 2 hours.