Comments (2)
Hello Lin!
thanks for your feedback :)
Regarding 1) if I understand correctly you want to have the coordinates of the inversions? There is approximate support for that (see here and also more details and a tutorial here. Note that by approximate I mean that CHROMEISTER loses a lot of precision while scaling down the comparison, so the breakpoint's coordinates will be approximate in plus/minus several thousand base pairs. If this is not good enough, I suggest you use GECKO for the particular region.
Regarding 2) I think this is a problem related to the visualization given the size of the sequences. CHROMEISTER is aimed at comparing chromosomes (although it also works for small ~1MB sequences). According to the coordinates in the plot, the sequences appear to be around 3,000 base pairs. In that case I recommend to run GECKO or BLAST. In fact, you can find information on how to do this on the Galaxy workflow manager here for free and without requiring command line.
Also, please note that at the moment I am unable to dedicate much time to this repo but if needed I will take a closer look during the weekend. Let me know if this helps!
Bests,
Esteban
from chromeister.
Thanks, I will try it.
from chromeister.
Related Issues (20)
- remove the [1] and null device from the stdout of both R scripts
- Comparison of large genomes.. messy plot HOT 9
- Sorting the plot from chromeister HOT 3
- compute_score.r error HOT 2
- get the coordinate of synteny block HOT 3
- parallel analysis HOT 1
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- coordinates from the events file HOT 4
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- Problem with run_and_plot_chromeister.sh
- error cannot open file 'dotplot.mat.csv': No such file or directory HOT 11
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- error of removal of "index-refseq-qryseq.csv" HOT 1
- Whole genome comparisons. HOT 1
- bring chromeister to bioconda and update galaxy tool HOT 20
- Error in axis - no locations are finite HOT 2
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