Single-cell RNA sequencing generated from 11 glioma patient samples
This dataset includes paired-end fastq files from 6 IDH-mutant, 5 IDH-wild-type glioma patient samples of unmatched initial and recurrent timepoints profiled using single-cell RNA sequencing.
- 11 samples
- DAC: EGAC00001002118
- Technologies: Illumina HiSeq 4000, Illumina NovaSeq 6000
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Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.
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