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It'd be nice to report the “window” regtools considered to decide each variant - junction pair were relevant to each other in the output file. This would make it easier if someone wanted to create a visualization of supporting data they already know what span of the genome is possibly relevant
The text was updated successfully, but these errors were encountered:
It'd be nice to report the “window” regtools considered to decide each variant - junction pair were relevant to each other in the output file. This would make it easier if someone wanted to create a visualization of supporting data they already know what span of the genome is possibly relevant
The text was updated successfully, but these errors were encountered: