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281
datasets available to search
ShareScore release 0.9.0
Dataset results
281 results for “copy number variation”
Representational Oligonucleotide Microarray Analysis (ROMA) array for Copy Number Variation Detection.
GEO Series GSE28013. Homo sapiens. 42 samples. Type: Genome variation profiling by genome tiling array.
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [Agilent021529]
GEO Series GSE96900. Homo sapiens. 2 samples. Type: Genome variation profiling by genome tiling array.
Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.
GEO Series GSE76437. Homo sapiens. 75 samples. Type: Genome variation profiling by SNP array.
DNA copy number variation analysis in hepatoma cell lines
GEO Series GSE77224. Homo sapiens. 20 samples. Type: Genome variation profiling by array.
Copy number variation comparison between control and CC214-2 resistant GBM39 xenografts
GEO Series GSE53042. Homo sapiens. 4 samples. Type: Genome variation profiling by SNP array.
Population structure shapes copy number variation in malaria parasites
GEO Series GSE75137. Plasmodium falciparum. 175 samples. Type: Genome variation profiling by genome tiling array.
3D genome of multiple myeloma reveals spatial genome disorganization associated with copy number variations
GEO Series GSE87585. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Genome variation profiling by high throughput sequencing.
Great Ape Copy Number Variation
GEO Series GSE30559. Gorilla gorilla gorilla; Pan paniscus; Pan troglodytes; Gorilla gorilla; Pongo pygmaeus; Pongo sp.; Homo sapiens; Pongo abelii; Pan troglodytes troglodytes. 58 samples. Type: Genome variation profiling by genome tiling array.
Identification of copy number variations by array comparative genomic hybridization in multi-ethnic multiple myeloma patients
GEO Series GSE44745. Homo sapiens. 63 samples. Type: Genome variation profiling by genome tiling array.
Chromosome copy number variation in Cryptococcus neoformans influences virulence and occurs in isolates from AIDS patients
GEO Series GSE29675. Cryptococcus neoformans; Cryptococcus neoformans H99. 96 samples. Type: Genome variation profiling by genome tiling array.
Normalization of whole-genome SNP data from non-Hodgkin lymphoma patients for copy number variation.
GEO Series GSE47357. Homo sapiens. 53 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.
Copy number variation in tRNA isodecoder genes impairs mammalian development and balanced translation (RNA-seq)
GEO Series GSE223662. Mus musculus. 24 samples. Type: Expression profiling by high throughput sequencing.
Genotyping and analysis of chromosome copy number variation (CNV) from pediatric primary intracranial germ cell tumor
GEO Series GSE19349. Homo sapiens. 16 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 [ATAC-seq]
GEO Series GSE200783. Mus musculus. 32 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Germline Copy Number Variants are Associated with Methylation Variation in the Genome
GEO Series GSE114131. Homo sapiens. 24 samples. Type: Methylation profiling by array.
Subtypes of HPV-positive head and neck cancers are associated with HPV characteristics, copy number variations, PIK3CA mutation, and pathway signatures. [SNP]
GEO Series GSE74949. Homo sapiens. 72 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.
Global variation of copy number in the human genome_COMM
GEO Series GSE5173. Homo sapiens. 552 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP 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.
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.
ScienceDex guides
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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.