Open sengelen opened 1 week ago
Hi,@sengelen. Can you provide more information? You can pay attention to whether the memory overflows during program execution. At present, I am trying to find a solution to this problem. Perhaps you can first try splitting the input pod5 and bam into multiple ones, then perform methylation calls separately, and finally merge the output tsv to see if this problem can be solved.
Hi @xyfltq. I followed the loaded memory it was big but there was no memory overflows. I ran deepsignal3 in a container on 4 a100 GPU node with 80Gb memory. And yes in my previous workflow (guppy/tombo/deepsignal-plant) I split the data on scaffolds of the reference. So I can do the same thing in order to see if this is a problem of a part of my data or if it is really a problem of the number of reads.
Dear all
I tested deepsignal3 call_mods with sucess on a sample of 360000 reads but when I launched on the entire run (16M reads) I had this error :
First of all I thought it was due to big reads so I added a read of 1Mb in my sample of 360000 reads and all worked well. So the problem is not the size of the reads. Do you think it is due to the number of reads ? On the web they say the error is that if the size of the pickled data is > 4096, have you any idea ?
Thank you Stefan