Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
166
datasets available to search
ShareScore release 0.9.0
Dataset results
166 results for “CNV”
Global DNA hypomethylation in ovarian cancer (CNV_data)
GEO Series GSE146554. Homo sapiens. 40 samples. Type: Genome variation profiling by SNP array.
Genome-wide genotyping and CNV scan in IgA Nephropathy patients.
GEO Series GSE44974. Homo sapiens. 217 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
CNV Identification: Prostate Cancer (PCa) vs Benign Prostatic Hyperplasia (BPH) Human DNA Samples
GEO Series GSE79402. Homo sapiens. 18 samples. Type: Genome variation profiling by genome tiling array.
CNV analysis of normal brain and glioma samples II
GEO Series GSE161275. Homo sapiens. 36 samples. Type: Genome variation profiling by SNP array.
Chromosomal microarray analysis for validation of the NGS-based CNV detection results in clinical samples
GEO Series GSE73190. Homo sapiens. 53 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
The effects of chromosomal copy number variations (CNV) on transcriptional programs at single cell resolution in multiple myeloma
GEO Series GSE141299. Homo sapiens. 11 samples. Type: Expression profiling by high throughput sequencing; Other.
Copy number variant (CNV) and Single nucleotide polymorphism (SNP) of UCLA hESC lines
GEO Series GSE91072. Homo sapiens. 15 samples. Type: Genome variation profiling by SNP array.
Influence of ATM-mediated DNA damage response on genomic variation in human induced pluripotent stem cells (NimbleGen CNV)
GEO Series GSE78717. Homo sapiens. 8 samples. Type: Genome variation profiling by genome tiling array.
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [Agilent021850]
GEO Series GSE96904. Homo sapiens. 2 samples. Type: Genome variation profiling by genome tiling array.
Genome-wide consequences of compromised NMD and their relavence for variable clinical phenotype of patients with UPF3B mutations [CNV]
GEO Series GSE27412. Homo sapiens. 8 samples. Type: Genome variation profiling by SNP array.
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [IlluminaHumanOmni5Exome]
GEO Series GSE96893. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP array.
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [Agilent021529]
GEO Series GSE96900. Homo sapiens. 2 samples. Type: Genome variation profiling by genome tiling array.
Multi-omics data analysis for the JGOG3025-TR2 ovarian cancer cohort [OncoScan_CNV]
GEO Series GSE263437. Homo sapiens. 287 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Breast tumors: different structures of tumor cells [cnv]
GEO Series GSE80758. Homo sapiens. 45 samples. Type: Genome variation profiling by array.
Molecular analysis of high-grade serous ovarian carcinoma with and without associated serous tubal intra-epithelial carcinoma [CNV]
GEO Series GSE102085. Homo sapiens. 96 samples. Type: Genome variation profiling by SNP array.
Strains for eQTL CNV Analysis
GEO Series GSE10377. Mus musculus. 5 samples. Type: Expression profiling by array.
Genotyping and analysis of chromosome copy number variation (CNV) from pediatric primary intracranial germ cell tumor
GEO Series GSE19349. Homo sapiens. 16 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
CNV analysis of 869 individuals from the Philippines with cleft lip and/or cleft palate
GEO Series GSE212166. Homo sapiens. 869 samples. Type: Genome variation profiling by genome tiling array.
Modeling and modulation of RHO signaling in human iPSC-derived retinal organoids from patients with RHO-CNV
GEO Series GSE245545. Homo sapiens. 9 samples. Type: Expression profiling by high throughput sequencing.
Influence of ATM-mediated DNA damage response on genomic variation in human induced pluripotent stem cells (Affymetrix CNV)
GEO Series GSE78715. Homo sapiens. 20 samples. Type: Genome variation profiling by SNP array.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.