Transcriptome Sequencing

Explore the full potential of transcriptome research with Novogene’s Transcriptome Sequencing services, powered by Illumina, PacBio, and Oxford Nanopore. Our RNA sequencing can cover both coding and non-coding regions of the transcriptome, offering valuable insights into the intricate interactions within the transcriptome.

Whole transcriptome sequencing integrates mRNA sequencing with non-coding RNA analysis, which includes long non-coding RNA sequencing (lncRNA-seq), small RNA sequencing (sRNA-seq) and circular RNA sequencing (circRNA-seq). For deeper exploration of complex regions, our full-length transcript sequencing utilizes long read capabilities from PacBio and Oxford Nanopore platforms. Additionally, we offer tailored solutions for prokaryotic RNA sequencing and meta-transcriptome sequencing, enabling detailed analysis at both individual species and whole community levels. Novogene also provide single-cell RNA sequencing for high-resolution analysis of individual cell transcriptomes, spatial transcriptomic sequencing for mapping gene expression within tissue context, and FFPE RNA-seq for analyzing RNA from formalin-fixed paraffin-embedded samples.

Transcriptome analysis provides invaluable information on gene expression profiles under varying conditions, including alternative splicing, gene fusion events, novel transcript discovery and microbial population dynamics. These insights have broad applications across disease research, drug-resistance studies, environmental and health-related microbiome studies, food and water safety and agricultural health.

Empower your research with precise and versatile sequencing solutions from Novogene.