Hi all,
I am sorry if maybe I am not the first one with this question.
I would like to see some alignment files using IGV, but I am mainly interested in non-coding RNA (such as lncRNA or miRNA).
Is there a way to increase the number of transcripts showed in the feature track, including all the transcripts now annotated?
In other words, I expect to see lncRNA in some regions, I have the aligned reads there and I know that there is the lncRNA X in that position, but loading hg19 I can not see the exon/intron representation in the genome, in the lower track, is there a way to add these kind of information?
Thank you in advance for your reply and please let me know if my question is not clear, I will try to explain in a better way.
Kind regards,
Jennifer