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1,023
datasets available to search
ShareScore release 0.9.0
Dataset results
1,023 results for “copy number”
Analysis of copy number profiles of several tumor samples of same patient reveals the successive steps in tumorigenesis
GEO Series GSE19195. Homo sapiens. 78 samples. Type: Genome variation profiling by SNP array; Genome variation profiling by genome tiling array.
Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies.
GEO Series GSE223312. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Genome-wide copy number aberrations and methylation profiles in human colorectal lesions
GEO Series GSE35534. Homo sapiens. 172 samples. Type: Methylation profiling by genome tiling array; 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 0GyA family)
GEO Series GSE94093. Mus musculus. 10 samples. Type: Genome variation profiling by genome tiling array.
Copy number analysis of plasma cells from AL amyloidosis patients
GEO Series GSE89616. Homo sapiens. 118 samples. Type: Genome variation profiling by SNP array.
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [Agilent021365]
GEO Series GSE96898. Homo sapiens. 2 samples. Type: Genome variation profiling by genome tiling array.
Genome-Wide Copy Number Variation Analysis of Chinese Patients with Intellectual Disability
GEO Series GSE83414. Homo sapiens. 31 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Single-cell copy number analysis in melanoma
GEO Series GSE151409. Homo sapiens. 1 samples. Type: Expression profiling by high throughput sequencing.
Copy Number Variation of human hepatocellular carcinoma (HCC) and Cholangiocarcinoma (CCA) from the Thailand Initiative in Genomics and Expression Research for Liver Cancer (TIGER-LC)
GEO Series GSE76213. Homo sapiens. 304 samples. Type: Genome variation profiling by SNP array.
Genome-wide changes in DNA methylation and copy number play a role in deregulation of gene expression in osteosarcoma
GEO Series GSE12885. Homo sapiens. 58 samples. Type: Expression profiling by array; Genome variation profiling by genome tiling array; Methylation profiling by genome tiling array.
Analysis of copy number variants on chromosome 21 in Down syndrome-associated congenital heart defects
GEO Series GSE93004. Homo sapiens. 526 samples. Type: Genome variation profiling by array.
Evaluation of affinity-based genome-wide DNA methylation data: effects of CpG density, amplification bias and copy number variation
GEO Series GSE24546. Homo sapiens. 40 samples. Type: Methylation profiling by genome tiling array; Methylation profiling by high throughput sequencing; 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 20mGyZ familly).
GEO Series GSE95336. Mus musculus. 14 samples. Type: Genome variation profiling by genome tiling array.
Genomic copy number variations in the genomes of leukocytes predict prostate cancer clinical outcomes
GEO Series GSE70650. Homo sapiens. 273 samples. Type: Genome variation profiling by SNP array.
High-resolution map of copy number variations in motor cortex of Control and Sporadic Amyotrphic Lateral Sclerosis patients by using a customized exon-centric comparative genomic hybridization array.
GEO Series GSE107375. Homo sapiens. 40 samples. Type: Genome variation profiling by array.
DNA copy number alterations in endobronchial squamous metaplastic lesions predict lung cancer
GEO Series GSE23644. Homo sapiens. 58 samples. Type: Genome variation profiling by array.
Acquired Genomic Copy Number Aberrations and Survival in Adult Acute Myelogenous Leukemia
GEO Series GSE23452. Homo sapiens. 226 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.
Primary tumor grafts as advanced models for breast cancer that authentically reflect tumor histopathology, growth, metastasis, and patient outcomes (copy number)
GEO Series GSE32530. Homo sapiens. 24 samples. Type: Genome variation profiling by SNP array.
DNA copy number, including telomeres and mitochondria, assayed using next-generation sequencing
GEO Series GSE21159. Homo sapiens. 3 samples. Type: Genome variation profiling by high throughput sequencing.
Investigation of MET copy number in various cancer cell lines
GEO Series GSE77414. Homo sapiens. 21 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.