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281
datasets available to search
ShareScore release 0.9.0
Dataset results
281 results for “copy number variation”
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.
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.
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.
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.
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.
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [Agilent023642]
GEO Series GSE96906. Homo sapiens. 2 samples. Type: Genome variation profiling by genome tiling array.
Hi-C As A New Tool For Precise Detection And Characterization Of Chromosomal Rearrangements And Copy Number Variation In Human Tumors
GEO Series GSE81879. Mus musculus; Homo sapiens. 10 samples. Type: Other.
Analysis of copy number variations among Chinese cattle breeds
GEO Series GSE47086. Bos grunniens; Bos taurus; Bubalus bubalis. 30 samples. Type: Genome variation profiling by genome tiling array.
Copy number variation of genes (exons) in invasive Cottus compared to the parental species, Cottus rhenanus and Cottus perifretum.
GEO Series GSE93064. Cottus perifretum; Cottus rhenanus; Cottus. 24 samples. Type: Genome variation profiling by array.
Copy number variation analysis of human Barrett's esophagus stem cells (HumanOmniZhongHua-8 v1.0 Beadchip)
GEO Series GSE68662. Homo sapiens. 8 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Genome-wide survey of large rare copy number variations in Alzheimer’s disease among Caribbean Hispanics
GEO Series GSE33528. Homo sapiens. 1215 samples. Type: Genome variation profiling by SNP array.
Chromosome copy number variation in Cryptococcus neoformans influences virulence and occurs in isolates from AIDS patients: CBS7779 black and white strains
GEO Series GSE29627. Cryptococcus neoformans; Cryptococcus neoformans H99. 17 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 GSE76438. Homo sapiens. 661 samples. Type: Genome variation profiling by genome tiling array; Genome variation profiling by SNP array.
Copy number variation of individual cattle genomes using next-generation sequencing.
GEO Series GSE31018. Bos taurus. 5 samples. Type: Genome variation profiling by genome tiling array.
Detection of genomic copy number variations induced by multiple DNA breaks
GEO Series GSE90027. Arabidopsis thaliana; Saccharomyces cerevisiae. 129 samples. Type: Genome variation profiling by genome tiling array.
Analysis of Genomic Copy Number Variation in Equine Recurrent Airway Obstruction
GEO Series GSE63033. Equus caballus. 56 samples. Type: Genome variation profiling by array.
Chromosome copy number variation in Cryptococcus neoformans influences virulence and occurs in isolates from AIDS patients: clinal and environmental strains
GEO Series GSE29671. Cryptococcus neoformans H99; Cryptococcus neoformans. 79 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.