Transcriptomics reveals how genes are expressed across different cells, tissues, and biological conditions, providing valuable insights into gene regulation, disease mechanisms, and biological function. Supported by comprehensive RNA sequencing workflows, multiple sequencing platforms, and end-to-end bioinformatics, our transcriptomics solutions help researchers answer a broad range of biological questions. Explore the services below to find the right solution for your study.
Profile protein-coding gene expression to identify differentially expressed genes, uncover biological pathways, and investigate disease mechanisms across a wide range of research applications.
Capture both coding and non-coding RNAs for comprehensive transcriptome profiling, enabling the study of gene regulation, long non-coding RNAs, and transcript diversity.
Capture full-length transcripts to identify transcript isoforms, alternative splicing events, gene fusions, and novel transcripts with greater accuracy.
Explore the complete transcriptome by analysing coding and non-coding RNA species, providing a comprehensive view of gene expression and transcriptional regulation.
Characterise microRNAs, piRNAs, siRNAs, and other small RNAs to investigate gene regulation, development, disease progression, and biomarker discovery.
Identify and quantify circular RNAs to explore their regulatory functions, biomarker potential, and roles in disease biology.
Characterise actively expressed genes within microbial communities to investigate functional activity, microbial interactions, and environmental responses.
Analyse bacterial and archaeal transcriptomes to investigate gene expression, regulatory pathways, stress responses, and host-microbe interactions.
Access a comprehensive portfolio of genomics technologies and platforms through a single trusted partner.
One partner for your entire transcriptomics workflow, from sample extraction, library preparation, sequencing to bioinformatics.
Included with bioinformatics analysis projects for intuitive RNA-seq analysis and biological interpretation.
Projects with bioinformatics analysis include complimentary access to NovoMagic Plus for intuitive RNA-seq analysis and interactive data visualisation.
Talk to our specialist to find the right solution.
Transcriptomics reveals how genes are expressed across different cells, tissues, and biological conditions, providing valuable insights into gene regulation, disease mechanisms, and biological function. Supported by comprehensive RNA sequencing workflows, multiple sequencing platforms, and end-to-end bioinformatics, our transcriptomics solutions help researchers answer a broad range of biological questions. Explore the services below to find the right solution for your study.
Profile protein-coding gene expression to identify differentially expressed genes, uncover biological pathways, and investigate disease mechanisms across a wide range of research applications.
Capture both coding and non-coding RNAs for comprehensive transcriptome profiling, enabling the study of gene regulation, long non-coding RNAs, and transcript diversity.
Capture full-length transcripts to identify transcript isoforms, alternative splicing events, gene fusions, and novel transcripts with greater accuracy.
Explore the complete transcriptome by analysing coding and non-coding RNA species, providing a comprehensive view of gene expression and transcriptional regulation.
Characterise microRNAs, piRNAs, siRNAs, and other small RNAs to investigate gene regulation, development, disease progression, and biomarker discovery.
Identify and quantify circular RNAs to explore their regulatory functions, biomarker potential, and roles in disease biology.
Characterise actively expressed genes within microbial communities to investigate functional activity, microbial interactions, and environmental responses.
Analyse bacterial and archaeal transcriptomes to investigate gene expression, regulatory pathways, stress responses, and host-microbe interactions.
Access a comprehensive portfolio of genomics technologies and platforms through a single trusted partner.
One partner for your entire transcriptomics workflow, from sample extraction, library preparation, sequencing to bioinformatics.
Included with bioinformatics analysis projects for intuitive RNA-seq analysis and biological interpretation.
Projects with bioinformatics analysis include complimentary access to NovoMagic Plus for intuitive RNA-seq analysis and interactive data visualisation.
Talk to our specialist to find the right solution.