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Nanopore sequencing offers advantages in all areas of research. Our offering includes DNA sequencing, as well as RNA and gene expression analysis and future technology for analysing proteins.

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New insights into large genomes white paper

This review outlines how researchers are now utilising the advantages of long nanopore sequencing reads to address this challenge, delivering more accurate large genomes for a wide variety of applications.

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Overview:

Since Haemophilus influenzae became the first organism to have its entire genome sequenced in 1995, there are now thousands of completed genomes covering archaea, bacteria and eukarya. However, the term ‘completed genome’ (or sometimes ‘finished genome’) is overused, as the majority of sequenced genomes contain numerous gaps. These gaps correspond to repetitive regions and structural variants that are too large to be resolved by the short-read sequencing technologies often used to generate the genomes.

Large genomes white paper
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