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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 analysis of in-trans correlations between copy number and expression with application to human breast cancer
GEO Series GSE10583. Homo sapiens. 20 samples. Type: Genome variation profiling by array.
caArray_socci-00214: TCGA Analysis of Copy Number for OV Using Agilent Human Genome CGH Microarray Kit 244K
GEO Series GSE90928. Homo sapiens. 87 samples. Type: Genome variation profiling by genome tiling array.
Copy number profiling of gastric cancer cell lines and gastric tumor tissues
GEO Series GSE22694. Homo sapiens. 132 samples. Type: Genome variation profiling by genome tiling array.
Assessment of tumor heterogeneity, as evidenced by gene expression profiles, pathway activation, and gene copy number, in patients with multifocal invasive lobular breast tumors [gene expression]
GEO Series GSE79058. Homo sapiens. 76 samples. Type: Expression profiling by array.
Copy number analysis of spontaneously transformed hTERT-immortalized ovarian surface epithelial cells
GEO Series GSE25492. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP array.
Nasopharyngeal carcinoma cell lines (copy number analysis)
GEO Series GSE15051. Homo sapiens. 6 samples. Type: Genome variation profiling by SNP array.
Genetic Copy Number Variants in Myocardial Infarction Patients with Hyperlipidemia
GEO Series GSE31276. Homo sapiens. 40 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Nasopharyngeal carcinoma cell lines (expression analysis and copy number analysis)
GEO Series GSE15098. Homo sapiens. 10 samples. Type: Expression profiling by array; Genome variation profiling by SNP array.
Copy number variations analysis by CytoscanHD array of 33 human pleural mesothelioma cell lines
GEO Series GSE134349. Homo sapiens. 33 samples. Type: Genome variation profiling by SNP array.
Retrospective study of 186 fetuses with sex chromosomal copy number variations
GEO Series GSE208389. Homo sapiens. 185 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.
Assessment of tumor heterogeneity, as evidenced by gene expression profiles, pathway activation, and gene copy number, in patients with multifocal invasive lobular breast tumors
GEO Series GSE79171. Homo sapiens. 160 samples. Type: Expression profiling by array; Genome variation profiling by array.
Prevalence of Copy-number neutral LOH in glioblastomas revealed by analysis of laser-microdissected tissues
GEO Series GSE10922. Homo sapiens. 28 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Impact on Disease Development, Genomic Location and Biological Function of Copy Number Alterations in Non-Small Cell Lung Cancer
GEO Series GSE34140. Homo sapiens. 301 samples. Type: Genome variation profiling by SNP array.
Concurrent DNA copy number alterations and mutations in genes related to maintenance of genome stability in uninvolved glandular tissue from breast cancer patients
GEO Series GSE63623. Homo sapiens. 180 samples. Type: Genome variation profiling by genome tiling array.
Copy Number Variants at Chromosome 10q11.21, 12p12.1 and 21q22.11 May Be Associated with Hyperlipidemia in Taiwanese Patients
GEO Series GSE38149. Homo sapiens. 7 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.
Copy number variation analysis of 18,000 fetuses in southern China
GEO Series GSE274505. Homo sapiens. 60 samples. Type: Genome variation profiling by SNP array.
Gene copy number polymorphism, a major source of genetic variation between humans
GEO Series GSE4981. Homo sapiens. 9 samples. Type: Genome variation profiling by array.
Genomic copy number variation in head and neck squamous cell carcinoma cell lines
GEO Series GSE127231. Homo sapiens. 35 samples. Type: Genome variation profiling by SNP array.
Genome-wide copy number profiling of 18 gastric cancer cell lines using 500K SNP arrays
GEO Series GSE51074. Homo sapiens. 50 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Copy number variation in tRNA isodecoder genes impairs mammalian development and balanced translation
GEO Series GSE227363. Mus musculus. 62 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Other.
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.