Review
Copyright ©The Author(s) 2016.
World J Gastrointest Oncol. Nov 15, 2016; 8(11): 772-785
Published online Nov 15, 2016. doi: 10.4251/wjgo.v8.i11.772
Figure 1
Figure 1 Bar chart showing the most frequently mutated genes in esophageal cancer according to catalogue of somatic mutations in cancer database. In the Y-axis the percentage of observed mutation frequency is represented. In the X-axis the most frequently mutated genes are listed. A: Top 30 mutated genes in esophageal adenocarcinoma; B: Top 30 mutated genes in esophageal squamous cell carcinoma.
Figure 2
Figure 2 Bar chart showing the copy number variations in esophageal cancer according to the study performed[13]. In the Y-axis the percentage of CNV frequency is represented. In the X-axis the most frequently altered genes are listed. A: Genes most commonly affected by CNV (amplification or loss) in esophageal adenocarcinoma; B: Genes most commonly affected by CNV (amplification or loss) in esophageal squamous cell carcinoma. CNV: Copy number variation.
Figure 3
Figure 3 Bar chart showing the most frequently mutated genes in gastric cancer according to catalogue of somatic mutations in cancer database. In the Y-axis the percentage of observed mutation frequency is represented. In the X-axis the genes are listed.
Figure 4
Figure 4 Copy number variation in the most important treatment targetable genes in gastric cancer. In the Y-axis the percentage of observed CNV is represented. In the X-axis the genes are listed. CNV: Copy number variation.
Figure 5
Figure 5 Bar chart showing the most frequently mutated genes in gastrointestinal stromal tumors according to catalogue of somatic mutations in cancer database. In the Y-axis the percentage of observed mutation frequency is represented. In the X-axis the genes are listed. GIST: Gastrointestinal stromal tumors.
Figure 6
Figure 6 Copy number variation in the most important treatment targetable genes in colorectal cancer. CNV: Copy number variation.