Closed lmulroney closed 1 year ago
I fixed this bug sometime ago as I remember. Can you please tell me which version of f5c you are using please?
I just realized that I'm using a fairly old version, v0.6.
I will update to v1.3 and try again.
Updating the version to v1.3 has fixed the issue. Sorry for the bother and thanks for the suggestion.
Hi @hasindu2008,
I'm trying to run F5C on an sample of 16M direct RNA nanopore reads, but I'm getting a segmentation fault at the same point roughly 200k reads into the sample. I've gotten warning about too many threads, which I've tried reducing. I've tried allocating more memory, and I've tried removing the last read written to the output to try and get past this segmentation fault that is happening always at the same point. I would appreciate any help. here is the last few lines of the log
[sprintf_append::WARNING][1;33m Too long string got truncated: 88.1937,96.7707,113.925,88.1937,96.7707,96.7707,113.925,101.059,113.925,113.925,113.925,113.925,101.059,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,122.502,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,118.213,122.502,113.925,113.925,113.925,113.925,113.925,118.213,113.925,113.925,113.925,113.925,113.925,113.925,113.925,122.502,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,118.213,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.925,113.9
......
[0m [sig_handler::ERROR][1;31m I regret to inform that a segmentation fault occurred. But at least it is better than a wrong answer.[0m
Here is the command: f5c_x86_64_linux eventalign -t 12 --iop 12 -r basecalled.fastq -b mapped.bam -g ref.fa --rna --print-read-names --scale-events --samples --min-mapq 0 --secondary=yes -o f5c_eventalign.tsv
Thanks, Logan