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. 2021 Jul 22;13(8):e12881. doi: 10.15252/emmm.202012881

Figure 1. Study design.

Figure 1

Schematic of ctDNA detection in matched CSF, plasma and urine samples from HGG and LGG patients using INVAR and/or sWGS. CNS, central nervous system; CSF, cerebrospinal fluid; HGG, high grade glioma; LGG, low grade glioma; sWGS, shallow whole‐genome sequencing.