Transcriptomics

Transcriptomics provides a highly sensitive and precise way for researchers to measure transcription across the genome at the single-nucleotide level. In particular, RNA sequencing (RNA-seq), enables the comprehensive assessment of transcript levels, identification of genes with differential expression and alternative splicing events, and the detection of single nucleotide polymorphisms (SNPs) and insertions/deletions (InDels), making it an indispensable tool in modern biological research.

Novogene, a leader in genomics and transcriptomics services, provides an extensive array of RNA-seq solutions, including sequencing of both coding and non-coding RNAs and whole transcriptome analysis through RNA-seq technologies. These services aim to elucidate the complex interactions between coding and non-coding RNAs in eukaryotic organisms, leveraging the power of transcriptomics and RNA-seq to advance our understanding of genetic regulation and function.

Whether you are utilizing meta-transcriptomic sequencing services to facilitate the analysis of prokaryotic species at both the individual and community levels, or employing Iso-seq for the in-depth analysis of full-length transcript isoforms, Novogene’s expertise in RNA-seq and transcriptomics is dedicated to helping you achieve your research objectives.

Experience the convenience and efficiency of Novogene’s RNA-seq and transcriptomics services with our end-to-end solutions. We offer a diverse range of library preparation options and support multi-platform capabilities on leading sequencing platforms such as the Illumina NovaSeq and the PacBio long reads platforms. Further enhance your RNA-seq data analysis with our complimentary bioinformatics tools, available on the NovoMagic platform, specifically designed for projects like ‘Human mRNA-seq’ and ‘Plant and Animal Eukaryotic mRNA-seq with reference’, integrating the latest advancements in RNA-seq and transcriptomics.