Hello, I have code that indicates there are a number of SNP mutations at specific locations for different cell types and none for others. I need to align all the respective long reads at that coordinate to see if my code works. These BAM files are located on a remote server and are too large for me to download them locally to my computer. I am really stuck, can anyone help me out? It is my first time doing this and I've never used IGV before. Happy to answer any questions that might help clarify what I need.
Sorry to be a noob, but what does the -L region.bed do? As in could you provide an example? I feel in over my head.
the manual is available here: http://www.htslib.org/doc/samtools-view.html