“…In total, 5743 patients with advanced GI cancers, including colorectal (n = 2791), gastric (n = 1141), esophageal (n = 369), pancreatic (n = 652), biliary tract (n = 416), liver (n = 67), small intestine (n = 93), appendiceal (n = 47), anal canal cancers (n = 13), GI stromal tumors (n = 79), and neuroendocrine tumors (n = 75), were enrolled. The landscape of genomic alterations was comparable to that reported in other profiling studies in Western countries, and revealed a high prevalence of mutations in trunk genes such as TP53 , and a considerable number of alterations were detected at a low prevalence showing a “long‐tail” distribution 10‐14 . RNA sequencing performed using the OCA assay aided the successful identification of rare fusions involving ERBB2 , FGFR2 or 3 , RET , ROS1 , NTRK , and others.…”