Liu Yang
Liu Yang
Thank you for your suggestion! But the fisrt step I have tried is --fast5 and --fastq. Disappointingly, this step did not work . My fast5 file has no Analyses Group...
Hello, My goal is to measure the polyA length of cdna in large quantities using tailfindr or PolyACaller with SQK-PCS111, both of which require a trace table. Rebasecalling with stand-alone...
Hello, Is this feature added in this new version ?
And for large genomes, memory usage is also very scary, the peak memory usage of `modkit pileup` reached 150G, and `modkit find-motifs` has exploded a server with 500GB of memory....
I have read the documention of Performance Consideration；but it has almost no effect on my doubts. For 300GB input files, the memory has already exploded before seed searching step
I have read the documention of Performance Consideration；but it has almost no effect on my doubts. For 300GB input files, the memory has already exploded before seed searching step
I have read the documention of Performance Consideration；but it has almost no effect on my doubts. For 300GB input files, the memory has already exploded before seed searching step
my modkit version : 
I found the problem. The problem is that the output folder must exist, otherwise an error will occur after creating the folder.
The reason I found seems inaccurate because I encountered this error again. Looking forward to software updates