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I ran POLCA with default parameters:
polca.sh -a $ASMFILE -r 'read1.fastq.gz read2.fastq.gz' -t 64 -m 20
However, I cancelled the job after 20 hours on a single fungal genome (~45Mb) and after over 11 million intermediate files were created (mostly .bam files). Is this supposed to happen? I have executed the code from both my HPC server installation and from a conda environment and I obtained the same result. This seems like this is not supposed to happen as this is supposed to be a fast and accurate tool to use. Are the intermediate files not being disposed of properly during the job?
Any help would be apreciated!
The text was updated successfully, but these errors were encountered:
Hi,
I ran POLCA with default parameters:
polca.sh -a $ASMFILE -r 'read1.fastq.gz read2.fastq.gz' -t 64 -m 20
However, I cancelled the job after 20 hours on a single fungal genome (~45Mb) and after over 11 million intermediate files were created (mostly .bam files). Is this supposed to happen? I have executed the code from both my HPC server installation and from a conda environment and I obtained the same result. This seems like this is not supposed to happen as this is supposed to be a fast and accurate tool to use. Are the intermediate files not being disposed of properly during the job?
Any help would be apreciated!
The text was updated successfully, but these errors were encountered: