Comments (5)
Hi. It seems that there are two issues. First is that the program is crashing. And second is that too few SNPs were identified.
The first issue seems to be a bug. Can you please share the log file so that I could have more information about the run?
For the second issue, can you please check how many SNPs are identified when using the show-snps
utility from MUMmer? SyRI can only report SNPs which are identified by the MUMmer alignments. So, it would be worthwhile to first check whether are indeed SNPs present in the alignments or not. Additionally, please also upload the snps_GARB.txt file.
from syri.
show-snps produce 17107349。 The syri.log is blank.
from syri.
The snps_GARB.txt file. I sent to your email
from syri.
Hi. A blank log file is quite strange. That could mean that SyRI was not running properly at all. Could you please check the installation again, and also the command that you are using.
Also, I didn't receive any email. Could you please check that you used the right email address.
from syri.
There was a bug affecting SNP identification. It should be fixed now and you should be getting proper number of SNPs.
from syri.
Related Issues (20)
- ERROR - No syntenic region found for chromosome: chr15. This is potentially caused by the two assemblies having different strands for this chromosomes. Reverse complement the chromosome to ensure that the same strands are analysed. Exiting HOT 1
- Syri doesn't deal with unequal chromosome comparison HOT 2
- IndexError: list index out of range(direction) HOT 6
- chroder input format requirements HOT 2
- ImportError: libicui18n.so.56: cannot open shared object file: No such file or directory HOT 2
- Sequence length calculation error HOT 6
- translocation ascross chromosomes HOT 1
- Can't install on Ubuntu 22.04 HOT 2
- How to cite chroder? HOT 1
- error running syri: IndexError: list index out of range HOT 2
- How to identify breakpoint of large inversion HOT 3
- Aligning bacterial genomes with different number of contigs HOT 2
- longer processing time for large genome? HOT 1
- nearly identical HDRs HOT 3
- How long does it take to generate the result file? HOT 3
- conda installation HOT 2
- Removes 'low-quality alignments' - what does this mean? HOT 1
- complicated region not detected correctly HOT 2
- About InvOut and Inv breakpoints HOT 3
- Huge chromosome problem HOT 6
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