Hi everybody,
I just did a alignment by STAR, and I am pretty sure the BAM output has some chimeric connections among different chromosomes, but I do not know how to visualize them, whereas I do see the chimeric conections in the same chromosome. is this something related to the samples being paired-end instead single-end reads? Is there any way to see them on IGV? Because I could not find one that works.
Thanks in advance!.
Thanks for your useful suggestion!I am trying to use your tool, but actually I am having some trouble to run the algorithm, I am not sure but maybe because i am dong RNAseq and not NGS. If you have any clue what is happening I'd appreciate it! T