A wide range of library preparation kits is available to suit whole-genome as well as targeted sequencing requirements. Amplification-free kits allow direct sequencing of short to ultra-long fragments of native DNA, eliminating PCR bias and allowing the detection of base modifications alongside standard nucleotides. Amplification-based kits enable whole-genome sequencing from low-input amounts or low-quality DNA (e.g. FFPE)
The only portable, real-time devices for DNA and RNA sequencing, giving complete control and creativity over when, where and how often you sequence, regardless of application.
High-coverage nanopore sequencing in formats ranging from modular, fully-integrated devices, to high-throughput solutions. Each flow cell can deliver the lowest price per Gb for nanopore sequencing.
The RNA library preparation kits offer a range of benefits, including high accuracy, long reads, and fast turnaround times. Every research project is unique, so to cater to different research projects, a range of kits are available. Confidently characterise and quantify full-length RNA transcripts, splice variants, and fusions using short to ultra-long fragment nanopore sequencing. Accurately analyse differential gene expression and transcript usage. Sequence native RNA directly, without amplification or reverse transcription, and identify base modifications.