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1,023
datasets available to search
ShareScore release 0.9.0
Dataset results
1,023 results for “copy number”
Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumour tissue
GEO Series GSE85035. Homo sapiens. 6 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 (Primary screening for 0mGyS familly).
GEO Series GSE92410. Mus musculus. 16 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.
Copy number analysis of selumetinib-resistant CRC cells lines
GEO Series GSE126367. Homo sapiens. 10 samples. Type: Genome variation profiling by 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.
Somatic copy number alterations associating with alcohol drinking and smoking in head and neck squamous cell carcinoma
GEO Series GSE47443. Homo sapiens. 225 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.
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (2X244K)
GEO Series GSE28187. Homo sapiens. 72 samples. Type: Genome variation profiling by genome tiling 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.
Combined clinical and genomic signatures for the prognosis of early stage non-small cell lung cancer based on gene copy number alterations
GEO Series GSE72195. Homo sapiens. 142 samples. Type: Genome variation profiling by genome tiling array; 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 0GyD family1)
GEO Series GSE94097. Mus musculus. 12 samples. Type: Genome variation profiling by genome tiling array.
Copy number variant (CNV) and Single nucleotide polymorphism (SNP) of UCLA hESC lines
GEO Series GSE91072. Homo sapiens. 15 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 20mGyU familly).
GEO Series GSE95494. Mus musculus. 20 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 (Secondary screening for 20mGyAA familly).
GEO Series GSE95340. Mus musculus. 14 samples. Type: Genome variation profiling by genome tiling array.
Genome-wide copy number profiling of MCF-7 and fulvestrant-resistant MCF-7/FR cells by SNP microarray.
GEO Series GSE121631. Homo sapiens. 2 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.
Copy number alterations of 103 hepatocellular carcinomas with hepatitis C virus etiology
GEO Series GSE9845. Homo sapiens. 197 samples. Type: Genome variation profiling by SNP array; SNP genotyping 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 0GyB family)
GEO Series GSE94094. 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 0mGyT familly).
GEO Series GSE92527. Mus musculus. 14 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.