Compute the genome read coverage

To interpretate the likelihood of translocation calls, we need to know the sequencing depth at the breakpoints.

This can be done by computing the genome read coverage from the BAM alignments, using the tool:

bamCoverage generates a coverage bigWig file from a given BAM or CRAM file (Galaxy Version 3.1.2.0.0)

BAM/CRAM file: Dataset Collection and Map with BWA-MEM on collection 3 (mapped reads in BAM format)
Bin size in bases: 100
Scaling/Normalization method: Do not normalize or scale
Coverage file format: bigWig
Compute an exact scaling factor: no
Region of the genome to limit the operation to: Leave empty
Show advanced options: yes
Ignore missing data?: yes
Other options unchanged