Distinguishing circular RNA reads from reads derived from the linear host transcript is a challenging task because of sequence overlap. We developed a computational approach, CiLiQuant, that determines the relative circular and linear abundance of transcripts and gene loci using back-splice and unambiguous forward-splice junction reads generated by existing mapping and circular RNA discovery tools.
Keywords: RNA; bioinformatics; circular; linear; splicing.
Copyright © 2022 Morlion, Hulstaert, Vromman, Anckaert, Everaert, Vandesompele and Mestdagh.