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.
166
datasets available to search
ShareScore release 0.9.0
Dataset results
166 results for “CNV”
A composite map of copy number variable (CNV) regions in the horse genome and the discovery of CNVs involved in equine XY disorders of sexual development
GEO Series GSE55266. Equus caballus. 44 samples. Type: Genome variation profiling by array.
CNV analysis of iPS cell lines and H2A.X knockout ES cell
GEO Series GSE42266. Mus musculus. 9 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 [IlluminaHumanOmni5]
GEO Series GSE96895. 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 [IlluminaCytoSNP850K]
GEO Series GSE96723. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP array.
CNV analysis of normal brain and glioma samples
GEO Series GSE123682. Homo sapiens. 15 samples. Type: Genome variation profiling by SNP array.
X-linked CNV burden and male infertility
GEO Series GSE37948. Homo sapiens. 200 samples. Type: Genome variation profiling by genome tiling array.
Analysis of copy number variation (CNV) in human induced hepatic progenitor cells (hiHepPCs) by aCGH
GEO Series GSE118910. Homo sapiens. 4 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 [IlluminaHumanOmni2.5Exome]
GEO Series GSE96846. 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 [IlluminaHumanOmniExpressExome]
GEO Series GSE96791. 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 [IlluminaHumanOmni2.5]
GEO Series GSE96810. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP array.
Affymetrix SNP array data (Oncoscan CNV) for Fudan University Shanghai Cancer Center Triple Negative Breast Cancer (FUSCCTNBC) project
GEO Series GSE118527. Homo sapiens. 424 samples. Type: Genome variation profiling by genome tiling array.
Effects of hydroxyurea on CNV induction in the mouse germline
GEO Series GSE114754. Mus musculus. 110 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 [Agilent022060]
GEO Series GSE96905. Homo sapiens. 2 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 [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.
A BRCA1 coiled-coil domain variant disrupting PALB2 interaction predisposes to mammary tumors with a targetable defect in homologous recombination repair [CNV-seq]
GEO Series GSE182449. Mus musculus. 101 samples. Type: Other.
CNV in spruce
GEO Series GSE92329. Picea mariana; Picea engelmannii x Picea glauca; Picea glauca. 73 samples. Type: Genome variation profiling by 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.
Detection of CNV in LMP1 mouse lymphomas
GEO Series GSE136074. Mus musculus. 12 samples. Type: Genome variation profiling by genome tiling array.
Oligo array for CNV calling AUTS2 project [Bluegnome]
GEO Series GSE37656. Homo sapiens. 1 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.