Comments (7)
Hi Linda. Can you please share the log file? Was there a warning message complaining about too many inverted alignments?
from syri.
Hi,
I attached the syri.log file.
Syri.log states this indeed. How can i resolve this?
thank you.
Linda
from syri.
That means that potentially your assemblies have different strands for that chromosome. Reverse complement the chromosome/s (for which you get this warning) and try again. This is described in more detail in the README.
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Hi, I did the reverse complement for all contigs mentioned in the log file, but after i ran nucmer and syri again, i still get the same message for 4 of the contigs. So changing to the reverse complement did not work for these 4. What can i additionally try? For the other contigs it shows output.
from syri.
The basic assumption with syri is that the compared sequences would be homologous to each other, i.e. they would be largely syntenic. Since, these four contigs did not work in both cases, I suspect that they might not be homologous. You could check if that is the case with these four contigs.
If the compared sequences are not homologous, then syntenic region cannot be identified and as a result syri cannot work.
Additionally, comparing highly divergent sequences would not result in biologically relevant structural rearrangements anyway.
from syri.
Hi,
I removed the most conflicting contigs and now i am left with this error:
Traceback (most recent call last):
File "/lustre/scratch/WUR/PRI/bakke227/tools/syri/syri/bin/syri", line 216, in
startSyri(args, coords[["aStart", "aEnd", "bStart", "bEnd", "aLen", "bLen", "iden", "aDir", "bDir", "aChr", "bChr"]])
File "syri/pyxFiles/synsearchFunctions.pyx", line 367, in syri.pyxFiles.synsearchFunctions.startSyri (syri/pyxFiles/synsearchFunctions.cpp:13271)
File "syri/pyxFiles/tdfunc.pyx", line 511, in syri.pyxFiles.tdfunc.getCTX (syri/pyxFiles/tdfunc.cpp:16911)
File "syri/pyxFiles/tdfunc.pyx", line 447, in syri.pyxFiles.tdfunc.readAnnoCoords (syri/pyxFiles/tdfunc.cpp:14839)
ValueError: invalid literal for int() with base 10: '14270551.0'
(END)
How can i solve this?
thanks for your help.
from syri.
Hi Linda. The log file contains a warning that the pandas version is 0.18.0. SyRI was designed using pandas version 0.23.4. I guess, that this might have caused this problem. Please check the installation guide here. Upgrading pandas (and then reinstalling SyRI) might solve this issue.
Other than this, I do not see any obvious reason for this error in the current log file. If the problem persists after upgrading pandas, than could you please run SyRI with DEBUG mode of logging and then share the new log file.
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Related Issues (20)
- 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
- keyerror HOT 3
- Request for Guidance on Converting NOTALs to Presence in Syri Outputs HOT 3
- translocated to different chromosomes HOT 3
- Consult DUP/INVDP for details HOT 2
- microhomology at ends of insertions HOT 4
- INV vs INVDUP HOT 2
- ERROR syri:201 - Length of query sequence of Chr1 is less than the maximum coordinate of its aligned regions HOT 7
- Wrong CIGAR string HOT 1
- IndexError: list index out of range syri HOT 9
- SYRI:IndexError: list index out of range HOT 1
- how to merge SyRI vcfs HOT 2
- Questions about 'NOTAL' HOT 2
- Question about output
- Support for promer HOT 3
- CIGAR string starting with non-matching base HOT 1
- Overlapping INV and SYN HOT 3
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