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Hello, I'm using nanopolish call-methylation on an Ontario long read data with an average read depth of 35. I'm using 40 processors with 4 GB of memory per processor. I'm using the standard parameters (-t, -r, -b, -g). The job has been running for 12 days, and it has only completed processing chromosomes 1-4 and 10-22 so far. I'm wondering if there are ways to speed up the process, or if this long processing time is expected for this tool?
The text was updated successfully, but these errors were encountered:
Likely to be the fast5 IO bottleneck
You may try https://github.com/hasindu2008/f5c/ with the --iop option to spawn parallel processes for IO. F5c should give same output as nanopolish.
Thank you for the quick and helpful response. I will try your suggestions. I am wondering if it is possible to use intervals (one Chr per job) when running the Nanopolish call-methylation and the calculate_methylation_frequency.py, and at the end concatenate the methylation_frequency.tsv files from each chromosome into a single file?
Hello, I'm using nanopolish call-methylation on an Ontario long read data with an average read depth of 35. I'm using 40 processors with 4 GB of memory per processor. I'm using the standard parameters (-t, -r, -b, -g). The job has been running for 12 days, and it has only completed processing chromosomes 1-4 and 10-22 so far. I'm wondering if there are ways to speed up the process, or if this long processing time is expected for this tool?
The text was updated successfully, but these errors were encountered: