E50a5f0d-c339-4494-9d1d-f2b7961701dd - samples
Ontology highlight
ABSTRACT: Paired end shallow whole genome sequencing (sWGS) data (FASTQ) for the identification of genomewide somatic copy number alterations (SCNA) and the estimation of tumor fractions.
PROVIDER: EGAD00001010293 | EGA |
REPOSITORIES: EGA
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