Hi,
I have 100 bigwig files and a bed file which has 80 features. I want to load all the bigwig files and bed annotation file in IGV and for each feature I want to output an image which has for each feature all the loaded 100 bigwig files. In total I should have 80 graphs(for 80 features). Also I want it to scroll and not a screen shot as I want to see all the bigwig files. I am writing a batch script as told in IGV but I cannot get all the bigwig files to display.
Any help how to do it is appreciated.
Thanks
In the "screenshot" categorie, check this paper : Strategies for identification of somatic variants using the Ion Torrent deep targeted sequencing platform. They have "created an IGV batch script to load the samples in which each variant was called", it's pretty nice.