What software tool is proper for the gap closing of the de novo produced illumina bacterial genome contig, and what can be installed through brew or sudo apt?
What software tool is proper for the gap closing of the de novo produced illumina bacterial genome contig, and what can be installed through brew or sudo apt? And what other tools are used for the contig preprocessing before submitting it to the annotation with RAST, Prokka, BG7?
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You can’t magically close gaps without more sequencing.
Are you looking for scaffolding programs?
OK, advise good scaffolding programs, which are easily installed on Linux Mint, thx. How do you define a scaffold and how to process it?
Why don’t you tell us what you actually want to achieve first? If you don’t know what a scaffold is or what to do with it, why would you want to scaffold?