Full-length transcriptome sequencing provides end-to-end coverage of transcripts, enabling accurate isoform profiling, alternative splicing analysis, detection of fusion transcripts, and discovery of novel RNA species. Leveraging PacBio SMRT long-read sequencing, researchers can obtain high-confidence, assembly-free full-length cDNA reads for precise characterization of transcript diversity across medical, agricultural, and functional genomics studies. In parallel, Oxford Nanopore direct RNA Sequencing captures continuous, native RNA molecules without reverse transcription or PCR, preserving RNA modifications, poly(A) tail length, and structural information to reveal post-transcriptional regulation with exceptional depth.
With extensive long-read sequencing experience, advanced PacBio and Nanopore platforms, and rigorous quality standards, Novogene delivers highly accurate, reproducible, and comprehensive full-length transcriptome data.
