RNA SEQUENCING SERVICES

We provide RNA sequencing using Nanopore and downstream bioinformatics analysis.

RNA SEQUENCING APPLICATIONS

Genetics

Cell fate and differential expression studies

viruses

Characterization of viral transcriptomes such as viruses with complex genomes

diseases

Studies of alternative splicing events for complete understanding of gene transcription and associated diseases (e.g, neurological diseases)

cancer therapy

Identification and characterization of fusion gene transcripts in cancer cells

MEDICINE

Disease diagnosis, prognosis and therapeutic selection

TUPAC.BIO SERVICES AND DOWNSTREAM SOFTWARE

Transcriptome analysis‍

We can perform RNA-seq and downstream analysis to determine gene expression changes in cell fate studies or other applications.

RNA-seq for Genome Annotation

We can perform long-read RNA sequencing and use the data for genome annotation.

Other

Considering RNA-sequencing for your research? Get in touch to discuss your research objectives.

ADVANTAGES OF NANOPORE RNA SEQUENCING

Direct sequencing of RNA molecules

RNA reads are generated while avoiding the PCR amplification biases, generating sequence analysis with base alterations and polyadenylation.

Isoform characterization and alternative splicing analysis

Long-read sequencing improves alternative splicing detection by capturing entire transcripts within single reads, and can be used to resolve the complex gene structure through the direct observation of underlying exon combinations.

Nanopore technology has been used as a tool for investigating changes in splicing in cancer-associated mutations.

Ultra-long, continuous RNA read generation

Nanopore technology has been used as a tool for investigating cancer-associated gene mutations that cause alternative splicing.

If you have any inquiries get in touch with us and we'll get back to you right away.