● Complete Plasmid Sequencing: Analyze entire plasmid structures to identify unknown plasmids or confirm known constructs.
● Comprehensive Genome and Epigenome Sequencing: Obtain full genome assemblies for humans and other mammals, including detailed epigenetic profiles.
● RNA Sequencing: Quantify isoform expression from bulk or single-cell samples, providing insights into gene expression dynamics.
● Bacterial Genome Sequencing: Achieve high-quality microbial genome assemblies to study bacterial genetics and functions.
● 16S rRNA and Metagenomic Analysis: Perform full-length 16S rRNA gene sequencing for precise microbial identification or conduct metagenomic studies to explore complex microbial communities.
● Ultra-Long DNA Sequencing: Generate ultra-long reads for detailed genome assemblies, structural variant analysis, and comprehensive genomic studies.

As a certified service provider for Oxford Nanopore Technologies, Sesana Genomics utilizes cutting-edge GridION and P2 Solo devices to deliver high-quality sequencing data.

Advantages of Nanopore Sequencing:

● Direct Sequencing: Reads native DNA and RNA strands without the need for amplification or chemical labeling, preserving original nucleotide sequences and modifications.
● Versatile Read Lengths: Capable of sequencing fragments ranging from short to ultra-long lengths, facilitating various genomic research applications.