Hello,
I'm using igv_linux_2.11.4
I loaded my RNA-seq bam file which I aligned to the reference genome.
The coverage track and alignment track seem fine, but I found that some regions with low coverage number displays more aligned read.
I guess it's because of downsampling, but the problem is that I cannot change that option.
When I go into View->Preferences->ThirdGen, 'downsample reads' option is already disabled.
Apart from that, any settings I change in the View->Preference doesn't affect the displayed data.
What's the problem?
Thanks.