High-grade serous ovarian carcinoma tumour whole genome sequencing variants

Tumour somatic variants (in VCF format) called from paired tumour-germline whole genome sequencing (using IDT library preparation system followed by sequencing on Illumina NovaSeq platform) of three high-grade serous ovarian tumour samples. The dataset comprises three VCF variant files.

30/12/2024
3 samples
DAC: EGAC00001003451
Technology: Illumina NovaSeq 6000

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Metadata

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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.

Study ID	Study Title	Study Type
EGAS50000000770	Assessment of candidate high-grade serous ovarian carcinoma predisposition genes through integrated germline and tumour sequencing	Cancer Genomics

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID	File Type	Size	Located in