Long-read sequencing provides greater continuity across complex genomes and transcriptomes, supporting applications from de novo and telomere-to-telomere genome assembly to structural variation, native DNA methylation and full-length transcript analysis.

Novogene Europe provides long-read sequencing solutions using PacBio HiFi and Oxford Nanopore technologies, supported by European sequencing capability, scientific project support and bioinformatics expertise for genomic and transcriptomic research.

Long-read solutions for genome research

Explore long-read approaches for genome assembly, structural variation and phasing, native DNA methylation, genome annotation and comparative analysis. Flexible PacBio and Oxford Nanopore workflows support projects requiring greater resolution across complex genomic regions.

From full-length transcripts to isoform discovery

Long-read RNA sequencing enables researchers to characterise full-length transcripts, transcript diversity, alternative splicing, fusion transcripts and novel isoforms. Flexible workflows include PacBio full-length RNA approaches and Oxford Nanopore sequencing, including Direct RNA sequencing.

Explore the service flyer for an overview of Novogene Europe’s long-read sequencing capabilities, platform options and analysis support.