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1,023
datasets available to search
ShareScore release 0.9.0
Dataset results
1,023 results for “copy number”
Genome-Wide DNA Copy Number Analysis of Acute Lymphoblastic Leukemia Identifies New Genetic Markers Associated with Clinical Outcome
GEO Series GSE75671. Homo sapiens. 265 samples. Type: Genome variation profiling by genome tiling array.
DNA copy number variation from human Wilms' Tumor samples
GEO Series GSE29374. Homo sapiens. 5 samples. Type: Genome variation profiling by genome tiling array.
A compendium of myeloma associated chromosomal copy number abnormalities and their prognostic value
GEO Series GSE21349. Homo sapiens. 491 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array; Expression profiling by array.
Copy number analysis of liver metastases from colorectal cancer
GEO Series GSE63490. Homo sapiens. 140 samples. Type: Genome variation profiling by SNP array.
Global variation of copy number in the MCF7 genome
GEO Series GSE8508. Homo sapiens. 1 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Single Cell Whole Genome Amplification Technique Impacts the Accuracy of SNP Microarray Based Genotyping and Copy Number Analyses
GEO Series GSE24690. Homo sapiens. 56 samples. Type: Genome variation profiling by SNP array.
Identification of candidate predisposing copy number variants in familial and early-onset colorectal cancer patients
GEO Series GSE13429. Homo sapiens. 49 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
SNP copy number data from glioblastoma subcutaneous xenografts
GEO Series GSE14804. Homo sapiens. 21 samples. Type: Genome variation profiling by SNP array.
A first comparative map of copy number variations in the sheep genome
GEO Series GSE25122. Bos taurus; Ovis aries. 11 samples. Type: Genome variation profiling by genome tiling array.
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (Mapping250K_Nsp)
GEO Series GSE28105. Homo sapiens. 14 samples. Type: Genome variation profiling by SNP array.
Genomic copy number alterations as predictive markers of systemic recurrence in breast cancer
GEO Series GSE10128. Homo sapiens. 62 samples. Type: Genome variation profiling by genome tiling array.
Copy number analysis of high-grade osteosarcoma
GEO Series GSE33153. Homo sapiens. 32 samples. Type: Genome variation profiling by SNP array.
Copy Number Analysis of Renal Epithelial Neoplasms
GEO Series GSE9469. Homo sapiens. 20 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Patterns of gene expression and copy-number alterations in VHL disease-associated and sporadic ccRCC
GEO Series GSE14994. Homo sapiens. 229 samples. Type: Expression profiling by array; Genome variation profiling by SNP array.
Copy number variants in autism spectrum disorders
GEO Series GSE270110. Homo sapiens. 35 samples. Type: Genome variation profiling by SNP array; Genome variation profiling by array.
Basal-like Breast Cancer DNA copy number losses identify genes involved in genomic instability, response to therapy, and patient survival
GEO Series GSE10893. Homo sapiens. 504 samples. Type: Expression profiling by array; Genome variation profiling by genome tiling array; Genome variation profiling by SNP array.
Copy number variation analysis of pheochromocytoma and paraganglioma
GEO Series GSE61594. Homo sapiens. 41 samples. Type: Genome variation profiling by SNP array.
Copy number profiling of 45 human breast cancer cell lines on Affymetrix 100K SNP arrays
GEO Series GSE13696. Homo sapiens. 90 samples. Type: Genome variation profiling by SNP array.
Profiling of copy-number variation between DNA isolation from different tissues of BN and ACI rats
GEO Series GSE45308. Rattus norvegicus. 24 samples. Type: Genome variation profiling by genome tiling array.
Genome-wide copy number analyses reveal genomic abnormalities involved in transformation of follicular lymphoma [gene expression]
GEO Series GSE81183. Homo sapiens. 42 samples. Type: Expression profiling by 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.