Comments (11)
Thanks for reporting this. The grid update introduced an error which was only apparent if the -dimension parameter was used. It should be now fixed.
Please update your repository using "git pull origin", then compile the files again with "make all" within the /src folder and rerun your experiment.
As a sidenote, also remember that if your input FASTA sequence is a multifasta containing more than ~50 sequences, then you should used the alternative script:
Rscript $scriptdir/compute_score-nogrid.R dotplot.mat 2000
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My bad, I updated the repository but forgot to update the release package :-)
First, I assume you were able to generate the .png file of the dotplot and then proceeded to run GECKO with the guide_fastas script to generate the alignments.
NOTE: please update your whole chromeister and gecko repository (I have just pushed an update that improves precision in the alignments from GECKO) and the re-run your experiment completely.
Regarding your question, those coordinates are in the sequence.
Also, if you are interested in obtaining the alignments (as text, such as in blast) you can do now by running the "guided_fastas.sh" script with a 1 at the end, in this fashion (remember to update your repos and recompile):
bin/guidefastas.sh X.fasta Y.fasta hits-XY-dotplot.mat.hits 1000 100 60 32 1
The one at the end indicates you want the alignments --beware, if there are many long alignments it will take some time. You can disable this option by running it with a 0 at the end.
Additionally you can visualize the master.csv file here:
https://pistacho.ac.uma.es/
Just upload it by using the "Load frags from local" button.
Btw, may I ask the size of your sequences?
Best regards,
Esteban
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In the case of the .png dotplot, no, thats not possible due to how chromeister works.
However, what you could do is take the .csv that is output by GECKO after using the guide_fastas script, upload here https://pistacho.ac.uma.es/ and then filter by similarity. This will remove alignments that do not meet the similarity threshold. See an example:
Best regards,
Esteban
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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
- Interpretation of scores HOT 1
- coordinates from the events file HOT 4
- Get plots in pdf or svg formats? HOT 4
- Breakpoint about inversion HOT 2
- Problem with run_and_plot_chromeister.sh
- Bad Install due opencv-python HOT 1
- Not finding any synteny in test data HOT 7
- 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
- Look into the dotplot matrix format in galaxy
- Remove empty lines before she bang lines
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