Figure 1.

Mutation spectrum of baseline plasma and tissue samples from 43 patients CRC. The genes with a high mutation frequency among all patients are listed on the left and individual patients are represented by the columns. Mutation types of non-synonymous single nucleotide variant, SNV (single nucleotide variant), indel (insertion-deletion), gain(stop gain, non-sense mutation), and loss(stop loss, missense mutation) are represented by blue, orange, and dark, respectively.