Hi,
I was under the impression that the canonical genes set was a dataset of
non-redundant genes, with different isoforms clustered as a single,
representative transcript. However, I now came across the two ids
"uc002hra.1" and "uc010cvq.1", which are obviously two splice isoforms, and
yet they are both independently represented in the canonical gene dataset.
I would be very grateful if you could clarify what's going on.
Best,
Schragi
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