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.
1,283
datasets available to search
ShareScore release 0.7.1
Dataset results
1,283 results for “Copying”
Comparative oncogenomic analysis of copy number alterations in human and zebrafish tumors enables cancer driver discovery
GEO Series GSE38397. Danio rerio. 294 samples. Type: Genome variation profiling by high throughput sequencing.
Osteosarcoma Copy Number Analysis
GEO Series GSE12830. Homo sapiens. 20 samples. Type: Genome variation profiling by genome tiling array.
Genome wide analysis of copy number variation in NAFLD spectrum
GEO Series GSE55645. Homo sapiens. 49 samples. Type: Genome variation profiling by genome tiling array.
Benign Copy Number Changes in Clinical Cytogenetic Diagnostics by Array CGH
GEO Series GSE11815. Homo sapiens. 24 samples. Type: Genome variation profiling by genome tiling array.
Transcript copy number estimation using a mouse whole-genome oligonucleotide microarray (22k Linearity)
GEO Series GSE3508. Mus musculus. 10 samples. Type: Expression profiling by array.
Detection of de novo and homozygous copy number variants in 99 autism simplex trios
GEO Series GSE23765. Homo sapiens. 300 samples. Type: Genome variation profiling by array.
Small bowel adenocarcinoma copy number profiles are more closely related to colorectal than to gastric cancers
GEO Series GSE23418. Homo sapiens. 91 samples. Type: Genome variation profiling by 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 20mGyA familly).
GEO Series GSE95261. Mus musculus. 16 samples. Type: Genome variation profiling by genome tiling array.
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.
Recognition of copy-back defective interfering rabies virus genomes by RIG-I triggers efficient immune response against vaccine strains
GEO Series GSE196051. Lyssavirus rabies; Homo sapiens; Rabies virus SAD B19. 36 samples. Type: Expression profiling by high throughput sequencing; Other.
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.
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.