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. 2020 Jan 22;48(4):1764–1778. doi: 10.1093/nar/gkz1223

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© The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 3. — Distribution of chimeric RNAs in different EM categories, types of chimeras based on parental gene location, and fusion protein coding potential. The distribution of chimeric RNAs was examined at three stages along our filtering pipeline: All GTEx predictions (All-GTEx) (A), after removal of M/M (Non-M/M) (B), and with an additional frequency requirement (Non-M/M-Recurrent) (C). The number of chimeric RNAs is also plotted based on their frequency (D). (E) Percentage of chimeric RNAs harboring the canonical splicing donor sequence (AG/GT) at the 5′ junction (left) or canonical splicing acceptor sequence (AG/G) at the 3′ junction (right) is plotted. All four categories of chimeric RNAs (E/E, E/M, M/E and M/M) in the whole GTEx or recurrent groups were examined.