Comments (2)
Hi,
I think SibeliaZ might be helpful in this scenario, though you will have to find a way to postprocesss the results (or visualize them) to find the roots of the problem.
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Hi Simón,
You can certainly try to use SibeliaZ for this, but as Iila mentioned, you would have to post-process the results. There may be simpler ways to get to the bottom of your problem. For example, for the second issue, you can use BLAT or BLAST to align your scaffolds against the human reference. For the first issue, there might be specialized tools for doing this, for example https://github.com/dfguan/purge_dups.
Good luck with it,
Paul
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Related Issues (20)
- free -w erro
- How would it deal with phased genomes?
- SibeliaZ/spoa/vendor/bioparser/include/bioparser/parser.hpp:124:19: error: 'gzFile_s' was not declared in this scope
- Installation issues HOT 2
- please include ##sequence-region pragmas in blocks_coords output HOT 4
- more detailed description for output HOT 1
- Conda installation doesn't include maf_to_gfa1.py HOT 2
- support gzip'd input fasta HOT 1
- is it suitable for the very big genome? HOT 2
- Apply the tool to virus HOT 4
- Q on coverage, multi-genome alignment, and maf2synteny HOT 4
- (support oneTBB) fatal error: tbb/mutex.h: No such file or directory HOT 3
- Question about block_coords.gff output
- Unexpected output HOT 1
- PackagesNotFoundError: The following packages are not available from current channels: - sibeliaz HOT 4
- sibeliaZ outputs HOT 2
- # running issue
- Getting alignments after running with "-n"
- question about LCB determination
- SibeliaZ causes my Ubuntu session to close
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