Oxford Nanopore sequencing has the ability to sequence DNA in excess of 1Mb in length and full length transcripts.
Long reads are ideal for genome assembly. They can identify structural variation within genomes, provide a comprehensive view of transcript abundance, and characterize isoform usage.
We offer the following techniques for nanopore sequencing:
Whole genome sequencing
Multiplexed amplicon sequencing
Low input sequencing
Analysis and interpretation of long read sequencing produces new bioinformatic challenges. We can help with the analysis and offer range of services to fit your specific needs.
If you require a quote for service or want more information contact us using the below links.