Our facility offers a comprehensive suite of RNA Sequencing services, catering to a broad spectrum of genetic research needs. Utilizing state-of-the-art technology, we provide in-depth analysis of RNA to detect both known and novel genetic features, including transcript isoforms, gene fusions, and single nucleotide variants.

The RNA Sequencing service is designed to support a wide range of research applications, from basic biological studies to complex disease research and therapeutic development. By enabling the detection of the full spectrum of RNA species within a sample, our service provides invaluable insights into the functional elements of the genome, facilitating a deeper understanding of biological processes and disease mechanisms.

In addition to standard RNA Sequencing, we specialize in a range of tailored analyses to suit specific research objectives, including:

• Quantitative gene expression analysis to measure RNA levels across different conditions or treatments.
• Identification and characterization of novel transcripts, splice variants, and non-coding RNAs.
• Comprehensive analysis of gene fusions and alternative splicing events.
• Single-cell RNA-Seq for detailed cellular heterogeneity insights.

Leverage our expertise in RNA Sequencing to propel your research forward, unlocking the vast potential of genetic information with precision and reliability.