Sanger Sequencing

Sanger Sequencing

Achieve unmatched sequencing accuracy with BaseClear’s industry-leading Sanger sequencing services. Recognized as the gold standard for DNA sequencing, this method provides high fidelity, capillary electrophoresis-based readouts, ensuring superior precision and reproducibility for a wide range of genetic applications. Whether validating gene constructs, detecting mutations, or confirming CRISPR edits, our Sanger sequencing solutions deliver exceptional clarity, low error rates, and reliable, publication-ready results with rapid turnaround times.

Our services are optimized for plasmid sequencing, single gene analysis, targeted sequencing, and mutation detection, making them ideal for clinical, pharmaceutical, and academic research. With automated sample processing and scalable solutions, we provide consistent quality, whether for small scale projects or high throughput applications.

Key benefits include:

• Gold-standard accuracy for gene validation, CRISPR confirmation, and mutation analysis.
• Short to mid-length sequencing reads with unmatched clarity and reproducibility.
• Fast turnaround times to support time-sensitive research and diagnostics.
• Seamless workflow integration for academic, biotech, and clinical applications.

Enhance your genetic analysis with high accuracy Sanger sequencing and ensure confident, publication-ready results for every project.