The Long-Read Sequencing team specialises in generating high-quality, continuous sequences of DNA using cutting-edge long-read sequencing technologies such as Oxford Nanopore and PacBio.

By providing extended read lengths, this approach enables the resolution of complex genomic regions, structural variants, and repetitive sequences that are often difficult to analyse with traditional short-read methods. The team plays a critical role in biodiversity research, allowing the study of complex genomes across diverse species, improving genome assemblies for plants, animals, and microorganisms, and supporting conservation efforts. Its work contributes to understanding genetic diversity, evolutionary patterns, and the genetic basis of adaptation in various ecosystems.

The Long-Read Sequencing team are focused also on advancing genomic research, improving genome assemblies, and enabling comprehensive variant detection across various applications, including human genomics, rare diseases, and microbial studies.