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.
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:
WBL’s Direct RNA Sequencing offering is specifically designed to address the following types of analyses:
*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.
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.
NGS 3.0 data with fully streamlined bioinformatics pipelines.
Results within 14-21 days of your sample’s arrival at the lab.
Teams of dedicated researchers and project managers to support your research and development.
Direct access to an online portal for sample information and batch status at each step of the sequencing process.
