From Enriched DNA to Sequencing-Ready Libraries

Our library preparation workflows convert enriched DNA into sequencing-ready libraries through efficient adaptor ligation and indexing strategies.

 

Core Components
  • Adaptor ligation
  • Platform-compatible adaptors for NGS sequencing
  • Optimized for high ligation efficiency and minimal bias
  • Barcode / Index incorporation
  • Unique sample indexing for multiplex sequencing
  • Enables high-throughput sample pooling and demultiplexing

 

Key Features
  • High conversion efficiency from input DNA to library
  • Compatible with low-input and fragmented DNA (cfDNA)
  • Reduced duplication rates and amplification bias
  • Flexible workflows for:
  • Targeted panels
  • Methylation sequencing
  • Mutation detection

 

Applications
  • Targeted NGS panels
  • DNA methylation sequencing (bisulfite libraries)
  • Mutation profiling and variant detection
  • Multiplex sequencing workflows