At SmartLife Biosciences, we offer advanced long-read sequencing services using state-of-the-art technologies such as Oxford Nanopore. Our long-read solutions provide high-resolution insights into complex genomic regions that are difficult to resolve with short-read technologies.

Whether you're working on de novo genome assembly, structural variant detection, full-length transcript analysis, or epigenetics, our long-read expertise ensures accurate, high-quality results tailored to your research goals.

Key Advantages of Our Long-Read Sequencing Services:

• Access to Complete and Continuous Reads: Ideal for spanning large structural variants, repetitive regions, and full-length transcripts.

• Custom Solutions: We adapt our workflows to your specific sample types and research objectives, including amplicons, plasmids, microbial genomes, and more.

• High Accuracy Through Optimized Bioinformatics Pipelines: Our in-house expertise in polishing, assembly, and annotation ensures reliable and reproducible results.

• Fast Turnaround and Dedicated Support: From sample preparation to data analysis, our team offers personalized project support and clear, actionable insights.

• Flexible Data Delivery Options: Receive both raw data and comprehensive reports, with alignment to reference sequences or de novo assembly where needed.

Our long-read sequencing service is designed for researchers seeking in-depth, accurate genomic insights and the flexibility to explore complex genetic information with confidence.

Contact us to discuss your project or request a quote — we’re here to support you at every stage of your sequencing journey.