Hello, I'm working on a pipeline using Bash, Python, and R to process metagenomic datasets. One of the features I want to incorporate is producing coverage maps for some hits depending on the read counts associated with them.
I know how to do this using IGV or UCSC genome browser and the necessary .bam and .bai files. However I want to automate this process so I won't need to manually do it each time. Some preliminary googling hasn't yielded much useful data. I was curious if anyone was aware of any Bash, Python, or R packages that have this same functionality?
Any help would be awesome, thanks!