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1,283
datasets available to search
ShareScore release 0.7.1
Dataset results
1,283 results for “Copying”
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [Agilent022060]
GEO Series GSE96905. Homo sapiens. 2 samples. Type: Genome variation profiling by genome tiling array.
Copy number variations distinguish lung adenocarcinomas from squamous cell carcinomas
GEO Series GSE74948. Homo sapiens. 162 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 0GyG family)
GEO Series GSE94103. Mus musculus. 16 samples. Type: Genome variation profiling by genome tiling array.
DNA copy number gain at 1q23.3 is associated with poor survival in metastatic bladder cancer [Agilent]
GEO Series GSE39281. Homo sapiens. 94 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 20mGyAA familly).
GEO Series GSE93523. Mus musculus. 14 samples. Type: Genome variation profiling by genome tiling array.
Genome-wide copy number and allele-specific copy number analysis of choroid plexus tumors (II)
GEO Series GSE61363. Homo sapiens. 20 samples. Type: Genome variation profiling by SNP array.
Genomic landscape of copy number aberrations enables the identification of oncogenic drivers in hepatocellular carcinoma [tumor]
GEO Series GSE38323. Homo sapiens. 572 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Genome-wide identification of copy number variations in Holstein cattle from Baja California, Mexico, using high-density SNP genotyping arrays
GEO Series GSE54813. Bos taurus. 12 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Integrated copy number and transcriptomic profiling reveal novel oncogenic drivers and clinically significant biomarkers in adenoid cystic carcinoma [Agilent]
GEO Series GSE153228. Homo sapiens. 100 samples. Type: Genome variation profiling by genome tiling array.
Analysis of the Saccharomyces cerevisiae Pan-Genome Reveals a Pool of Copy Number Variants Distributed in Diverse Yeast Strains From Differing Industrial Environments.
GEO Series GSE26689. Saccharomyces bayanus; Saccharomyces cerevisiae. 98 samples. Type: Genome variation profiling by 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 0mGyX familly).
GEO Series GSE92526. Mus musculus. 16 samples. Type: Genome variation profiling by genome tiling array.
Using the Porcine SNP60k array to discover copy number variations in high and low fertility boars
GEO Series GSE66170. Sus scrofa. 36 samples. Type: Genome variation profiling by SNP array.
Copy number variation of human intestinal stem cells with different passage in culture (five pedifrees, passage 5 and 25)
GEO Series GSE66748. Homo sapiens. 11 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [IlluminaHumanCoreExome]
GEO Series GSE96816. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP array.
DNA Copy-Number Alterations in clear-cell Renal Cell Carcinoma (ccRCC) Tumors and Tumorgrafts for samples deficient in BAP1 or PBRM1
GEO Series GSE25540. Homo sapiens. 82 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 [IlluminaPsychArray]
GEO Series GSE96789. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP array.
High-resolution custom array spanning Xq28 region to study patients carrying MECP2 copy number gain (part 1)
GEO Series GSE49440. Homo sapiens. 22 samples. Type: Genome variation profiling by genome tiling array.
The dependency factor RRM2 at the nexus of a copy number driven regulatory network and a target for synthetic lethal interactions with replication stress checkpoint addiction in high-risk neuroblastom
GEO Series GSE161900. Homo sapiens. 54 samples. Type: Expression profiling by high throughput sequencing.
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 20mGyM familly).
GEO Series GSE95325. Mus musculus. 20 samples. Type: Genome variation profiling by genome tiling array.
Non-clonal mosaicism in human somatic and embryonic stem cells revealed by single-cell array-based copy-number variation analysis
GEO Series GSE51126. Homo sapiens. 106 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.