Hello,
Ximmer looks very promising, so I would really love to get it to work. Unfortunately, all tools return 1 and the very first hint of what is going wrong is:
Chromosome * is not analysable by CODEX and many more
which happens for each chromosome.
I tried to run Ximmer each time on only one tool to single out the source of error, but each tool aborts at some early point.
So, I guess my input is somewhat wrong. Are there any special limitations on the formats or so?
Here is what I use:
regular .bam files
a regular bed file with gene annotations like:
1 2234359 2234599 SKI
my config.groovy looks like the example from your documentation.
Hello, Ximmer looks very promising, so I would really love to get it to work. Unfortunately, all tools return 1 and the very first hint of what is going wrong is:
Chromosome * is not analysable by CODEX and many more
which happens for each chromosome. I tried to run Ximmer each time on only one tool to single out the source of error, but each tool aborts at some early point. So, I guess my input is somewhat wrong. Are there any special limitations on the formats or so? Here is what I use:
1 2234359 2234599 SKI
Here you can see the std out of Ximmer.
I would be really happy to use Ximmer and I am looking forward to hearing from you, Vinzenz