 | 1 | initial version |
I found GenomeBrowseto be a very good alternative to IGV for RNA-seq data. I only had two issueswhile looking at BAM files: (1) Is it possible to adjust the display parameters so that each coverage peak is normalized to the total number of reads in the BAM file? This would be very useful for visually comparing expression across samples. (2) Is it possible to export the plots as jpeg/pdf?
thank you!
