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281
datasets available to search
ShareScore release 0.9.0
Dataset results
281 results for “copy number variation”
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [IlluminaHumanOmni5]
GEO Series GSE96895. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP array.
Expression data and Copy Number Variations from Diffuse Large B Cell Lymphoma (DLBCL) patients
GEO Series GSE136971. Homo sapiens. 448 samples. Type: Expression profiling by array; Genome binding/occupancy profiling by genome tiling array.
Genome-wide analysis of copy number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes
GEO Series GSE212296. Homo sapiens. 1108 samples. Type: Genome variation profiling by genome tiling array.
Piperaquine Resistance is Associated with a Copy Number Variation on Chromosome 5 in Drug-Pressured Plasmodium falciparum Parasites
GEO Series GSE27907. Plasmodium falciparum. 4 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 [IlluminaCytoSNP850K]
GEO Series GSE96723. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP array.
Quantitative analysis of chromatin interactions upon copy number variation at mouse 4E2 [4C-seq]
GEO Series GSE64358. Mus musculus. 96 samples. Type: Other.
Detection of copy number variation in patients with Pelizaeus-Merzbacher disease (PMD) - Affymetrix
GEO Series GSE64121. Homo sapiens. 4 samples. Type: Genome variation profiling by SNP array.
Analysis of copy number variation (CNV) in human induced hepatic progenitor cells (hiHepPCs) by aCGH
GEO Series GSE118910. Homo sapiens. 4 samples. Type: Genome variation profiling by genome tiling array.
Copy number variation analysis on a non-Hodgkin lymphoma case-control study identifies an 11q25 duplication associated with diffuse large B-cell lymphoma
GEO Series GSE58718. Homo sapiens. 1349 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 [IlluminaHumanOmni2.5Exome]
GEO Series GSE96846. 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 [IlluminaHumanOmniExpressExome]
GEO Series GSE96791. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP array.
Gene copy number variation in male breast cancer by aCGH
GEO Series GSE23891. Homo sapiens. 25 samples. Type: Genome variation profiling by array.
A Map of Copy Number Variations in Chinese Populations
GEO Series GSE30481. Homo sapiens. 155 samples. Type: Genome variation profiling by SNP array.
Copy Number Variation at 16p11.2 Imparts Transcriptional Alterations in Neural Development in an hiPSC-derived Model of Corticogenesis
GEO Series GSE144736. Homo sapiens. 52 samples. Type: Expression profiling by high throughput sequencing.
Copy number variations may contribute to congenital heart defect risk greatly by disrupting long noncoding RNAs
GEO Series GSE201076. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
The cellular origin and malignant transformation of Waldenström's Macroglobulinemia [copy number variation]
GEO Series GSE61650. Homo sapiens. 59 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 [IlluminaHumanOmni2.5]
GEO Series GSE96810. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP array.
Rare Copy Number Variation in Extremely Impulsively Violent Males
GEO Series GSE116022. Homo sapiens. 281 samples. Type: Genome variation profiling by SNP array.
Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.
GEO Series GSE76436. Homo sapiens. 586 samples. Type: Genome binding/occupancy profiling by genome tiling array; Genome binding/occupancy profiling by SNP array.
Array CGH between GK and Wistar Rats for Detecting Copy Number Variations
GEO Series GSE21387. Rattus norvegicus. 3 samples. Type: Genome variation profiling by genome tiling 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.