Closed Wyclif3 closed 2 months ago
You are only having 40 reads. This does not look like as something as a genome or some well-covered / well-formed part of it.
This means some of the data are of low quality ? I already performed data cleaning in trimmomatic before assembling genes in hybpiper. What is the best solution for my problem at this point?
Description of bug
Spades is failing to assemble some of my reads. I have tried to change the Kmer values and the problem still persists with several abnormalities.
spades.log
spades.log
params.txt
spades_redo.log
SPAdes version
3.15.0
Operating System
linux
Python Version
3.8.4
Method of SPAdes installation
binaries
No errors reported in spades.log