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. 2018 Aug 18;34:46–60. doi: 10.1016/j.ebiom.2018.07.040

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© 2018 The Authors

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

PMC Copyright notice

Fig. 7 — Kaplan-Meier survival analysis of prognostic signatures based on seven types of alternative splicing events in gastrointestinal tract adenocarcinomas.

Prognostic signatures based on Alternate Acceptor site for esophageal adenocarcinoma (A), stomach adenocarcinoma (B), colon adenocarcinoma (C), and rectum adenocarcinoma (D).

Prognostic signatures based on Alternate Donor site for esophageal adenocarcinoma (E), stomach adenocarcinoma (F), colon adenocarcinoma (G), and rectum adenocarcinoma (H).

Prognostic signatures based on Alternate Promoter for esophageal adenocarcinoma (I), stomach adenocarcinoma (J), colon adenocarcinoma (K), and rectum adenocarcinoma (L).

Prognostic signatures based on Alternate Terminator for esophageal adenocarcinoma (M), stomach adenocarcinoma (N), colon adenocarcinoma (O), and rectum adenocarcinoma (P).

Prognostic signatures based on Exon Skip for esophageal adenocarcinoma (Q), stomach adenocarcinoma (R), colon adenocarcinoma (S), and rectum adenocarcinoma (T).

Prognostic signatures based on Mutually Exclusive Exons for esophageal adenocarcinoma (U), stomach adenocarcinoma (V), colon adenocarcinoma (W), and rectum adenocarcinoma (X).

Prognostic signatures based on Retained Intron for esophageal adenocarcinoma (Y), stomach adenocarcinoma (Z), colon adenocarcinoma (AA), and rectum adenocarcinoma (AB).