Genome wide analysis of tumours in individuals with p53-germline mutations
Direct links to NCBI, no account and no request form: the whole study as GSE34323_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 7 samples.
Also filed as BioProject PRJNA151479. Searching any of these in the dataset finder brings you back here.
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+ 7 more — browse all 7 samples with per-sample file links →
- GSE19416 Genome-wide copy number variation in TP53 mutation negative ovarian tumours 7 samples
- GSE34258 Genome sequencing of childhood medulloblastoma brain tumors links chromothripsis with TP53 mutations 49 samples
- GSE314342 Genome-scale perturb-seq in primary human CD4+ T cells reveals genes regulating T cell programs and human immune traits. 577 samples
- GSE15688 Acquired mutations in TET2 are common in myelodysplastic syndromes 122 samples
- GSE61502 Whole Genome Sequencing Informs Therapeutic Selection for Pancreatic Cancer 100 samples
- GSE341753 Cohesin loading at regulatory elements shapes 3D genome folding during erythropoiesis [RNA-Seq] 12 samples
- GSE29772 CNV analysis for Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations 6 samples
- GSE36138 SNP array data from the Cancer Cell Line Encyclopedia (CCLE) 947 samples
Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.