Detect the greatest number of variants
PCR-free means reduced library bias and gaps. The result is unsurpassed data quality. This enables you to detect the greatest number of variants. Excellent genome coverage means your results have the lowest and smallest number of gaps and enhanced coverage of high GC/AT rich regions.
Use PCR-free for faster protocols
The industry's most widely adopted sample preparation workflow for DNA sequencing is now enhanced. Removing PCR creates a faster protocol and superior data quality. Bead-based size selection shortens the workflow. In tandem with Illumina's sequencing systems, the TruSeq DNA PCR-Free Sample Preparation Kit provides a range of enhancements to the industry's most widely adopted sample preparation workflow.
Kits for limited available DNA and exome enrichment
TruSeq Nano DNA Sample Prep is also available for efficient interrogation of samples with limited available DNA.
For enrichment, the Nextera Rapid Capture Exome and Expanded Exome assays provide a seamless end-to-end library preparation solution. These all-in-one sample preparation and exome enrichment kits allow researchers to identify coding variants 70% faster than any other method. An expanded kit increases coverage to UTRs and miRNA.