
Officially recommendflye
to conduct sequence assembly in Nanopore website.
conda install -y flye
flye --nano-raw ~/project/ONT/basecalling_gpu_sup/pass/BL21.fastq.gz -g 4.6m -o ~/project/ONT/basecalling_gpu_sup/6_flye -t 15 -i 3
Output

View the assembled genome sequences

Using flye
to conducted genome assembly, we get two cycle sequences, one is about 5M in size (genome), and the other is about 11k in size (plasmid).
Taxonomy Analysis
After assembling, we start to classify them directly by using theKraken2
tools which is commonly used.
-
Taxonomy Analysis result

The output of kraken-report is tab-delimited, with one line per taxon. The fields of the output, from left-to-right, are as follows:
-
Percentage of reads covered by the clade rooted at this taxon
-
Number of reads covered by the clade rooted at this taxon
-
Number of reads assigned directly to this taxon
-
A rank code, indicating Unclassified, Domain, Kingdom, Phylum, Class, Order, Family, Genus, or Species..
-
The indented scientific name
网友评论