CNV | Copy number variation |
GB | Glioblastoma |
GCS | Global score |
MAF | Minor allele frequency |
PTI | Phylogenetic tree inference |
SNV | Single-nucleotide variant |
VAF | Variant allele frequency |
WES | Whole-Exome Sequencing |
CNV | Copy number variation |
GB | Glioblastoma |
GCS | Global score |
MAF | Minor allele frequency |
PTI | Phylogenetic tree inference |
SNV | Single-nucleotide variant |
VAF | Variant allele frequency |
WES | Whole-Exome Sequencing |