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. 2022 Feb 11;9:758464. doi: 10.3389/fmed.2022.758464

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Copyright © 2022 Choudhury, Tan, Shi, Tee, Ngeow, Poh, Goh and Mong.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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The spectrum of genomic alterations in NSCLC was detected by plasma NGS testing. Baseline plasma samples for 53 NSCLC cases were tested with the 49-gene panel LiquidHALLMARK® assay. Cases with ≥1 alteration are presented (n = 38), 15 cases with no alteration detected were excluded from the presentation. Genes with no alteration detected among all cases were also excluded from the presentation. Percentage (%) and number of cases carrying a mutation in each gene are shown in the right-most columns.