Open xhu556 opened 7 months ago
This is usually caused by low quality of sequences, which results in 0 contigs. In the current version, we don't have a filter to remove bad samples. You'd better to manually remove the bad samples. Suppose you found the sample "hts_smp1" caused the problem in the log file, then you can find all "hts_smp1" related files and remove them by
runFolder=/path/my/phytopipe/run
#find files
find $runFolder -name "hts_smp1*"
#remove files
find $runFolder -name "hts_smp1*" -exec rm {} \;
Now you can rerun the pipeline without fastqDir parameter since the read files are already in the raw folder. The pipeline will continue the previous work.
The PhytoPipe exits because of Error in rule run_blastx or run_blastn. How can I fix it?