Comments (3)
Thanks for mentioning this, I've had a few people trip up on the identity being decimal vs percentage so you aren't alone haha. Just merged #43 into master which adds some default values and more usage examples to the help menu so you can try pulling the newest version from git, otherwise it'll be in a new release sometime soon.
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Looks great, thanks for updating, and for the great tool!
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Closing this since it's included in version 0.0.14, which is now released :)
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Related Issues (20)
- Errors in using gff and faa file
- The output result has no information HOT 4
- some issues for -mo --matrix_out parameter HOT 2
- Locus inversion showing incorrect locations
- Possible bug in cluster similarity output (-mo option)
- -gf/--gene_functions not working?
- Problem with -gf and -cm parameteres HOT 3
- try example encouter error
- Gene and species limit HOT 1
- Broken pipe error when using clinker to plot gene clusters HOT 2
- Renaming coding sequence back to gene number HOT 3
- Running clinker via spyder
- Can different domains within a gene also be applicable? HOT 2
- Can't save changes to session HOT 2
- update 0.0.28 HOT 3
- the legend HOT 4
- How to visualize a gene on a large chromosome?
- Use clinker to visualize individual exons rather than whole gene?
- ValueError: not enough values to unpack (expected 2, got 1)
- Error in clinker HTML plotting function
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