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I'm trying to run your script on my bam file but the process dies due to memory lack (32GB RAM). I have partial output file my_sample.var with variants for 5 out of 9 chromosomes and I'm wondering is there any way to run script starting from chr6? (and then combine 2 output files). Or maybe there is some other way (e.g. saving data in temp. file rather than store in RAM) to overcome the memory problem. I am also wondering if my partial var. file is already filtered or should I filter them before further processing?
Best regards,
The text was updated successfully, but these errors were encountered:
You can split the genome into several chromosomes and get the mapping bam files from each chromosome. Use one linux command to run them all and combine the result.
Hi,
I'm trying to run your script on my bam file but the process dies due to memory lack (32GB RAM). I have partial output file my_sample.var with variants for 5 out of 9 chromosomes and I'm wondering is there any way to run script starting from chr6? (and then combine 2 output files). Or maybe there is some other way (e.g. saving data in temp. file rather than store in RAM) to overcome the memory problem. I am also wondering if my partial var. file is already filtered or should I filter them before further processing?
Best regards,
The text was updated successfully, but these errors were encountered: