A direct PCR approach is applied to our nanopore-based full-length 16S/18S/ITS sequencing, allowing the direct amplification of 16S/18S/ITS sequences from bacterial/archaeal/fungal/eukaryotic cell suspensions via PCR without DNA purification. This approach overcomes the limitations of the traditional culture-based bacterial identification, instead providing rapid and accurate microbial identification and diversity analysis. https://www.cd-genomics.co...