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Capture full-length transcript diversity with WBL's cDNA sequencing service, powered by Oxford Nanopore Technologies (ONT). This service provides detailed insights into gene expression, alternative splicing, and isoform diversity by sequencing the entire cDNA length, enabling a deeper understanding of transcriptomic landscapes and gene regulation.
Capture the full transcriptomic landscape across diverse species, resolving highly repetitive and other complex regions.
cDNA
Short Read RNA
ONT Direct RNA
RNA Sequencing
Small Nucleotide Variants
Methylation & Hydroxy Methylation
Structural Variants
Copy Number Variation
Repetitive Regions
Haplotype
Splice Variants
Fusion Transcripts
Humans
Animals
Plants
Bacteria*
Virus*
Poly(A)+ RNA
Total RNA
*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.
Accelerate your research with comprehensive nanopore data. With native precision and long reads, Wasatch BioLabs' Nanopore services deliver actionable insights with confidence in every read.
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Leverage Oxford Nanopore Technologies-certified services, supported by rigorous quality assurance and control metrics, to achieve reliable data for your research.
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Enhance your nanopore data with custom bioinformatics solutions, using tailored workflows and advanced analysis to generate impactful, publication-ready insights.
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Work directly with sequencing and bioinformatics experts who provide personalized, end-to-end support, guiding you from project planning to data interpretation.
cDNA sequencing involves reverse transcribing RNA into complementary DNA prior to sequencing, whereas direct RNA sequencing analyzes native RNA molecules without conversion. Direct RNA sequencing preserves RNA modifications, while cDNA sequencing offers higher throughput and improved error correction, making it well suited for large-scale gene expression and transcript diversity studies.
Wasatch BioLabs combines Oxford Nanopore long-read sequencing with expert bioinformatics support to deliver high-quality, full-length transcript data. Our approach enables accurate isoform detection, alternative splicing analysis, and transcript structure resolution beyond the limits of short-read sequencing.
Wasatch BioLabs accepts high-quality total RNA or poly(A)+ RNA from a wide range of non-infectious sources, including human, animal, plant, bacterial, and viral samples. All samples must be certified as non-infectious prior to submission. Questions regarding sample quality, preparation, or shipment can be directed to our team at support@wasatchbiolabs.com.
We apply quality control checks to assess RNA integrity prior to reverse transcription. If degradation is detected, our team provides guidance on sample re-preparation or workflow optimization to ensure cDNA libraries accurately reflect transcript content and minimize downstream artifacts.
Yes, we offer comprehensive bioinformatics support for cDNA sequencing data, including custom analysis workflows and one-on-one collaboration to support data interpretation and generation of publication-ready insights. Analysis options include isoform quantification, splice variant detection, expression profiling, and fusion transcript identification.
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