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.
1,023
datasets available to search
ShareScore release 0.9.0
Dataset results
1,023 results for “copy number”
Analysis of somatic DNA copy number alterations and frequency of breast cancer intrinsic subtypes from Mexican women
GEO Series GSE87049. Homo sapiens. 359 samples. Type: Expression profiling by array; 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.
Validation of dedifferentiated liposarcoma (DDLS) cell lines with the original tumors via copy number alteration analysis
GEO Series GSE184702. Homo sapiens. 5 samples. Type: Genome variation profiling by array; Genome variation profiling by high throughput sequencing.
Analysis of somatic DNA copy number alterations and frequency of breast cancer intrinsic subtypes from Mexican women [copy number]
GEO Series GSE87048. Homo sapiens. 200 samples. Type: Genome variation profiling by SNP array.
Analysis of transgenerational effects on DNA copy number aberrations in male mice exposed to continuous 20mGy/day gamma-rays for 400 days (Secondary screening for 20mGyJ familly).
GEO Series GSE95322. Mus musculus. 16 samples. Type: Genome variation profiling by genome tiling array.
Analysis of transgenerational effects on DNA copy number aberrations in male mice exposed to continuous 20mGy/day gamma-rays for 400 days (Primary screening for 20mGyX familly).
GEO Series GSE93508. Mus musculus. 18 samples. Type: Genome variation profiling by genome tiling array.
Radiation-specific DNA copy number aberration in rat mammary carcinoma.
GEO Series GSE16128. Rattus norvegicus. 21 samples. Type: Genome variation profiling by array.
Analysis of transgenerational effects on DNA copy number aberrations in male mice exposed to continuous 20mGy/day gamma-rays for 400 days (Secondary screening for 0GyE family)
GEO Series GSE94101. Mus musculus. 16 samples. Type: Genome variation profiling by genome tiling array.
Landscape of somatic allelic imbalances and copy number alterations in HER2-amplified breast cancer
GEO Series GSE31645. Homo sapiens. 26 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Copy number analysis of BPH (Benign Prostatic Hyperplasia)
GEO Series GSE124187. Homo sapiens. 36 samples. Type: Genome variation profiling by SNP array.
Cyto2.7M copy number analysis of eight diffuse large B-cell samples and one matched blood sample
GEO Series GSE37978. Homo sapiens. 9 samples. Type: Genome variation profiling by SNP array.
Deep Sequence Analysis of the Relationship between Gene Expression, CpG Island Methylation, and Gene Copy Number in Breast Cancer Cells
GEO Series GSE27003. Homo sapiens. 24 samples. Type: Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Across-species comprehensive copy number analyses identifies subtype-specific drivers of breast cancer development
GEO Series GSE52173. Mus musculus; Homo sapiens. 201 samples. Type: Genome variation profiling by SNP array.
Combined clinical and genomic signatures for the prognosis of early stage non-small cell lung cancer based on gene copy number alterations [Affymetrix]
GEO Series GSE72192. Homo sapiens. 78 samples. Type: Genome variation profiling by SNP array.
Representational Oligonucleotide Microarray Analysis (ROMA) array for Copy Number Variation Detection.
GEO Series GSE28013. Homo sapiens. 42 samples. Type: Genome variation profiling by genome tiling array.
Copy number of oral cell lines [CGH]
GEO Series GSE59406. Homo sapiens. 8 samples. Type: Genome variation profiling by array.
Screening for copy-number alterations and LOH in CLL - a comparative study of four microarray platforms
GEO Series GSE13557. Homo sapiens. 40 samples. Type: Genome variation profiling by SNP array; Genome variation profiling by genome tiling array.
Affymetrix OncoScan SNP arrays for profiling somatic copy-number alterations in primary renal diffuse large B cell lymphoma
GEO Series GSE270422. Homo sapiens. 29 samples. Type: Genome variation profiling by SNP array.
Copy number profiling of 5-FU resistant gastric cancer cell line compared to the parental cell line
GEO Series GSE89191. Homo sapiens. 1 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 [Agilent021529]
GEO Series GSE96900. Homo sapiens. 2 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.