Whole genome sequencing of glioblastoma reveals enrichment of non-coding constraint mutations in known and novel genes
|Study ID||Alternative Stable ID||Type|
Study Datasets 1 dataset.
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The dataset comprises of an aggregate level VCF (version 4.1), containing the somatic point and indel mutations found across the glioblastoma cohort (SweGBM-1, n=38 samples). The VCF file is in accordance with the HTS format specifications (https://samtools.github.io/hts-specs/).