SUPPA2 is able to quantify and report alternative last (AL) exon events, which is good, since the last exons are always the target of several factors such as miRNAs and regulators of mRNA stability and transport. But, what about alternative polyadenylation (pA) sites? Would it be possible to also include this feature in SUPPA2 script as well, if the input TPM files allow for this of course? if so, SUPPA2 will be the package that detects the most possible binary splicing events (excluding non-binary or complex events).
Dear Eduardo,
SUPPA2 is able to quantify and report alternative last (AL) exon events, which is good, since the last exons are always the target of several factors such as miRNAs and regulators of mRNA stability and transport. But, what about alternative polyadenylation (pA) sites? Would it be possible to also include this feature in SUPPA2 script as well, if the input TPM files allow for this of course? if so, SUPPA2 will be the package that detects the most possible binary splicing events (excluding non-binary or complex events).
Thank you!
Kind regards, Jamal.