Full-Length Transcriptome Sequencing uses long-read sequencing to capture complete RNA transcript sequences, helping researchers resolve transcript structures, isoform diversity, alternative splicing and gene expression complexity. This approach is particularly useful for transcript discovery, genome annotation, non-model organism research and studies where short-read RNA-seq cannot fully resolve transcript structure.
Novogene Europe supports poly(A)-based full-length transcriptome sequencing using PacBio Iso-Seq and Oxford Nanopore long-read RNA sequencing options. Bioinformatics workflows can support isoform characterisation, novel transcript identification, alternative splicing analysis, fusion transcript analysis, functional annotation and transcript-level expression analysis.
