De Novo Genomics is a certified Oxford Nanopore service provider. We offer a variety of sequence services options as well as bioinformatic analysis to fit your research needs. 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. 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.
We perform a wide array of analysis on data generated from next generation sequencing platforms.
We offer the following techniques for nanopore sequencing:
- Whole genome sequencing
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