Illumina Ngs Library Prep

Our enrichment library prep yields provides 90 on target reads 95 uniformity and low pcr duplicate rate across all illumina sequencing systems.

Illumina ngs library prep.

In five steps this guide walks you through the range of automation tools that exist for ngs library preparation and helps you find a solution that matches your application throughput and budget needs. These adapters contain the full complement of sequencing primer hybridization sites. Library preparation sequencing and data analysis. Our solutions support a broad range of sample types from cell.

Ask virtually any question related to the genome transcriptome or epigenome of any organism with ngs library prep kits optimized for illumina sequencers. Libraries are prepared by fragmenting a gdna or cdna sample and ligating specialized adapters to both fragment ends. Novel easy to use and fast solutions for both dna and rna library preparation. Illumina library prep protocols accommodate a range of throughput needs from lower throughput protocols for small labs to fully automated library preparation workstations for large laboratories or genome centers.

Find resources to help you prepare for each step and see an example workflow for microbial whole genome sequencing a common ngs application. Learn what to consider as you evaluate options for automating library preparation. Library preparation for the illumina sequencing platform requires inputs of a defined length therefore fragmentation of dna or the use of cdna prepared from rna is the starting point. Next generation sequencing involves three basic steps.

Our innovative ngs library preparation portfolio uses three key technologies. Illumina library prep protocols accommodate a range of throughput needs from lower throughput protocols for small labs to fully automated library preparation workstations for large laboratories or genome centers. Experience superior support across the entire workflow with kits. This is followed by end repair 3 and 5 to generate blunt ended phosphorylated molecules followed by the addition of a non templated da tail before.

Find out the benefits of each approach and how. Illumina library prep protocols can accommodate a range of throughput needs from lower throughput protocols for small laboratories to fully automated library preparation workstations for large laboratories or genome centers. A key element of illumina ngs is high quality library preparation. Use this simple selector tool to find easy to use ngs library prep kits optimized for illumina sequencers.

The other key technology used in our ngs library prep is adapter ligation long known for consistent high quality data. Filter by method species and more then compare share and order kits. 1 the workflow uses a single 90 min hybridization step and as little as 10 ng input dna. Find the right kit.

Fast and innovative. Discover your library prep kit.