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281
datasets available to search
ShareScore release 0.9.0
Dataset results
281 results for “copy number variation”
Validation experiment of copy number variations identified by next-generation sequencing in chickens (part 2)
GEO Series GSE54118. Gallus gallus. 3 samples. Type: Genome variation profiling by genome tiling array.
Genome-wide copy number variation in human metastatic melanoma cell lines
GEO Series GSE24890. Homo sapiens. 4 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males
GEO Series GSE8691. Homo sapiens. 57 samples. Type: Genome variation profiling by genome tiling array.
Profiling of copy-number variation in tumors from heterozygous and homozygous Tp53C273X knockout rats
GEO Series GSE55895. Rattus norvegicus. 28 samples. Type: Genome variation profiling by genome tiling array.
Diversity of Human Copy Number Variation and Multicopy Genes
GEO Series GSE24334. Homo sapiens. 5 samples. Type: Genome variation profiling by genome tiling array.
Copy number variation analysis of nasopharyngeal carcinoma cell lines
GEO Series GSE15172. Homo sapiens. 4 samples. Type: Genome variation profiling by genome tiling array.
Copy Number Variation data from non-trasformed human fibroblasts
GEO Series GSE231621. Homo sapiens. 129 samples. Type: Genome variation profiling by genome tiling array.
Genome wide analysis of copy number variation in NAFLD spectrum
GEO Series GSE55645. Homo sapiens. 49 samples. Type: Genome variation profiling by genome tiling array.
Copy number variation in fetal alcohol spectrum disorder
GEO Series GSE102650. Homo sapiens. 182 samples. Type: Genome variation profiling by SNP array.
Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity
GEO Series GSE101418. Homo sapiens. 52 samples. Type: Genome variation profiling by SNP array.
Validation experiment of copy number variations identified by next-generation sequencing in chickens
GEO Series GSE54119. Gallus gallus. 11 samples. Type: Genome variation profiling by genome tiling array.
Transgenic mice overexpressing Neuregulin-1 model neurofibroma-malignant peripheral nerve sheath tumor progression and implicate specific chromosomal copy number variations in tumorigenesis.
GEO Series GSE40212. Mus musculus. 12 samples. Type: Genome variation profiling by array.
Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity [Omni2.5M Beadchip]
GEO Series GSE101417. Homo sapiens. 31 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.
The UBC-40 Urothelial Bladder Cancer Cell Line Index [copy number variation]
GEO Series GSE64572. Homo sapiens. 50 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP 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.
Detection of copy number variation in patients with Pelizaeus-Merzbacher disease (PMD)
GEO Series GSE64122. Homo sapiens. 14 samples. Type: Genome variation profiling by SNP array; Genome variation profiling by genome tiling array.
Dosage compensation can buffer copy-number variation in wild yeast
GEO Series GSE61532. Saccharomyces cerevisiae. 60 samples. Type: Expression profiling by high throughput sequencing.
Genomic copy number variation induced by TAQing system in Arabidopsis thaliana.
GEO Series GSE90026. Arabidopsis thaliana. 115 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 [IlluminaHumanOmni5Exome]
GEO Series GSE96893. Homo sapiens. 2 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.