We use novel cost-effective library construction methods to provide fast and efficient sequencing services, sequencing in-house, and provide library only services for users wishing to outsource their sequencing to reduce costs further.

We offer a full range of services including:

• Short-Read Sequencing employs high-throughput technologies, providing cost-effective and rapid sequencing of DNA fragments
• Long-Read Sequencing captures extensive genomic regions, offering insights into complex structural variation , haplotypes, and repetitive elements, essential for de novo genome assembly and comprehensive genomic analysis
• Library and Pool Preparation services enables us to generate high quality libraries, including quantification of DNA and normalisation. We pool and can send to your preferred vendor for sequencing

We offer our Next Generation Sequencing services including consultancy for fee-for service through QIB Extra.