Closed carolhsb closed 3 years ago
Hi Carol, is that the whole log?
Best regards, Robert
Hi Carol, is that the whole log?
Best regards, Robert
Yes...
Might be that it got killed due to insufficient memory. How much RAM do you have and how big is the concat.clean.fastq.gz file?
Might be that it got killed due to insufficient memory. How much RAM do you have and how big is the concat.clean.fastq.gz file?
The concat.clean.fastq.gz file has 57GB and I got 250 GB of RAM
Can you please run gzip -dc concat.clean.fastq.gz | wc -c
? It will print the uncompressed file size.
I did it and the file has 173943628896
I think that this Illumina run will not fit into your RAM (or it will hit swap memory and take a long time finish), either with or without the wrapper.
I think that this Illumina run will not fit into your RAM (or it will hit swap memory and take a long time finish), either with or without the wrapper.
That's odd, because I've polished an assembly with PacBio subreads (166 G) in the same sever without any problems
For short reads, the overhead of storing them in memory (~1.5x FASTQ) is greater than for long reads (~1x FASTQ).
For short reads, the overhead of storing them in memory (~1.5x FASTQ) is greater than for long reads (~1x FASTQ).
Oh, I understand it. Thank you for your time
Best regards
Hopefully, we will update Racon in the near future to use less memory. :)
Hi Robert,
Me again. Racon runs without errors, but it outputs an empty fasta file. I've tried twice and got the same result. I'm using racon version 1.4.21.
This is the command I'm using: python3 /home/carol/racon/build/bin/racon_wrapper -t 30 --split 28048207 /home/carol/short_reads_mma/concat.clean.fastq.gz ./dbgAGAIN2.illumina.sam ./dbgAGAIN2.corrected.fasta > dbgAGAIN2.corrected2.fasta
This is the log: RaconWrapper::run] preparing data with rampler [RaconWrapper::run] total number of splits: 42 [RaconWrapper::run] processing data with racon [racon::Polisher::initialize] loaded target sequences 0.289602 s
Thank you,
Carol