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CIGAR and query sequence lengths differ for reads in smoothed.selective.bam #16
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Hi Kyle, thanks for trying SVDSS out. I encountered a similar issue some times ago, I tried to solve it with no success and then I forgot to go back to it.. Just to be sure that the issue is the same, can you please try to use the SVDSS version you find in the lowcov branch? Unfortunately, you'll have to compile it from scratch since it's a development branch and I didn't produce the binary yet.. I suspect that for those alignments, in the new version you should see a line starting with
(where If this is the case, I'll try to fix it. If you have any issue, please let me know. Other way to check this (in case you encounter any issue while compiling):
Let me know what you prefer. Best, |
Hi, I got the same error. I used pbmm2 to map raw fastq files and used the mapped bam files as input to SVDSS. After using smooth to obtain the smoothed.selective.bam file, I have the same problem. Below are the first 10 lines of smoothed.selective.bam. Do you have any thoughts on this issue? Thanks,
|
Thanks for the response,
Thanks |
I see. Well, at least we found the problem. I'll fix the smooth and let you know. In the meantime, can you please try to run the @YahGao I suspect your error is the same, so I'll let you know when it's solved. Best, |
I think I've fixed this. Please, check the new commit on the lowcov branch. So pull, recompile, and rerun the smoothing. You shouldn't see any warning anymore (or line starting with Regarding the Best, |
Please check the latest release v1.0.5. This bug should be fixed now. |
Hi,
I was trying to use this exciting tool to call SVs using HiFi reads on a genome assembled from those same reads.
I can run
SVDSS index
andSVDSS smooth
. The file smoothed.selective.bam is generated. When I runSVDSS search --assemble
the process completes generating files calledsolution_batch_*.assembled.sfs
, but the log contains the samtools error[E::bam_read1] CIGAR and query sequence lengths differ for m64069_220917_213940/14419164/ccs
multiple times for different reads.Because of this, I am unable to generate an index for the BAM
Meaning I cannot complete the pipeline.
I am able to index the BAM input to
SVDSS smooth
without issue.I have tried to filter the BAM for primary reads, but I run into the same problem.
Please let me know if you have any advice to overcome this issue.
Thanks
Kyle
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