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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.
Explore our other RNA Services
cDNA sequencing involves converting RNA into complementary DNA (cDNA) through reverse transcription, followed by sequencing. In contrast, direct RNA (dRNA) sequencing skips the conversion step, enabling the analysis of native RNA molecules. While dRNA preserves epigenetic marks, cDNA sequencing offers greater throughput and improved error correction, making it ideal for studying gene expression and transcript diversity across large datasets.
Wasatch BioLabs combines Oxford Nanopore Technologies with expert bioinformatics support to deliver full-length transcript sequencing with high accuracy. Their long-read capabilities allow for precise isoform detection, alternative splicing analysis, and transcript structure resolution—going beyond standard short-read sequencing providers. Personalized project guidance and certified ONT workflows ensure research-grade, publication-ready results.
Wasatch BioLabs accepts total RNA and poly(A)+ RNA from a variety of non-infectious sources, including human, animal, plant, bacterial, and viral samples. To ensure high-quality cDNA sequencing, samples should be properly extracted, free from contaminants, and certified as non-infectious. For guidance on preparation or shipment, clients can contact their support team for detailed protocols.
The lab employs quality control checkpoints to assess RNA integrity before reverse transcription begins. If samples show signs of degradation, our team offers consultation on sample re-preparation or optimization. This approach ensures the resulting cDNA libraries reflect accurate and comprehensive transcript information, minimizing artifacts in downstream cDNA analysis.
Wasatch BioLabs provides raw output data and can support comprehensive post-sequencing cDNA analysis, including isoform quantification, splice variant detection, expression profiling, and fusion transcript identification. Our bioinformatics experts tailor data pipelines based on research goals and deliver clear, structured reports suitable for academic, translational, or clinical studies.
