Next generation sequencing (NGS) is a method of high-throughput sequencing in which millions of DNA strands can be sequenced in parallel. Many researchers use NGS as an important tool to gain insight into the detailed and comprehensive genetic and epigenetic modifications of genomes from many different cell types. Choose from our comprehensive mix of kits to extract and prepare your library sample for NGS analysis.
Whether you are preparing samples for ChIP-seq, whole genome sequencing, or Bisuilfite-sequencing our kits are easy, efficient, and convenient.
Fast and Streamlined Procedure – Compact protocols with simple clean-up steps to save time and prevent handling errors, as well as loss of valuable samples
Highly Convenient – The kit contains all required components for each step of the library preparation for the most reliable and consistent results
Minimize bias – High quality enzymes achieve reproducibly high yields of nucleic acid library with minimal sequence bias and low error rates
Flexibility – Can be used for both non-barcoded (singleplexed) and barcoded (multiplexed) library preparation with broad range of nucleic acid input