Direct RNA.

Native Sequencing

Explore isoform-level resolution of the transcriptome with WBL’s Direct RNA Sequencing service. Leveraging Oxford Nanopore Technologies (ONT) Direct RNA Sequencing, WBL’s service enables the direct sequencing of full-length, native RNA transcripts without reverse transcription or amplification biases.

Direct RNA Sequencing allows researchers to sequence the transcriptome and visualize native epigenetic modifications, offering researchers and clinical service providers richer transcriptome data with unprecedented insights for multi-omics studies.

The Power Of Long Read Sequencing

Capture the full complexity of RNA molecules in their native state. ONT’s long-reads enable identification of full-length transcripts across diverse species, the resolution of highly repetitive and other complex regions, and the direct detection of post-transcriptional modifications.

Explore the advantages of WBL’s Long-Read Direct RNA Sequencing compared to cDNA and short-read RNA sequencing methods:

Direct RNA Sequencing:
Applications and Use Cases

WBL’s Direct RNA Sequencing offering is specifically designed to address the following types of analyses:

Direct RNA Sequencing:
Applications and Use Cases

*WBL currently only accepts DNA and RNA that are extracted from samples that are not classified as infectious. This policy ensures the safety of our laboratory personnel and compliance with regulatory standards. Please ensure that all samples are appropriately treated and certified as non-infectious before submission. If you have any questions about sample preparation or our safety standards, please contact our support team at: support@wasatchbiolabs.com.

Humans
Animals
Plants
Bacteria*
Virus*

Sample types accepted:

mRNA
tRNA
rRNA

WBL: Your Competitive Edge

Maximize your sequencing output with WBL’s leading technology, streamlined bioinformatics pipelines, and expert guidance. WBL’s team of researchers are pioneers in Oxford Nanopore Technologies sequencing with decades of experience in genomics and bioinformatics research.

Robust Data

NGS 3.0 data with fully streamlined bioinformatics pipelines.

Fast Turnarounds

Results within 14-21 days of your sample’s arrival at the lab.

Expert Guidance

Teams of dedicated researchers and project managers to support your research and development.

Full Visibility

Direct access to an online portal for sample information and batch status at each step of the sequencing process.

Specialized offerings in our next-generation     biolab

Explore our other RNA Services