Closed akkellogg closed 8 years ago
@akkellogg Sorry for the late reply, i'm just returning from holiday. What type of data are you working with? Exome or genome?
@zeeev We think we pinpointed the problem. We were aligning the reads to a custom reference and we think the issue was with that reference, since aligning to a different reference seems to have solved the problem.
Hello,
I'm having a problem running WHAM on some smaller BAM files. Every time I try to run it the WHAM.err file returns the following:
INFO: WHAM-BAM will using the following fasta: ../ABL1_cds.fasta INFO: OpenMP will roughly use 24 threads INFO: target bams: S2.bam INFO: gathering stats for each bam file.
At which point it exits out and prints "Floating Point Exception" to the terminal.
The reads are aligned with BWA-MEM, and duplicates marked with Picard. Any idea what would be causing this issue? My BAM file is relatively small, could this be causing the problem?
Thanks for your help.
-Ana