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.
281
datasets available to search
ShareScore release 0.9.0
Dataset results
281 results for “copy number variation”
Auricular Malformations Driven by Copy Number Variations in a Hierarchical Enhancer Cluster and Dominant Enhancer Recapitulates Human Pathogenesis [RNA-seq]
GEO Series GSE263086. Mus musculus. 10 samples. Type: Expression profiling by high throughput sequencing.
Data from: Genome reduction uncovers a large dispensable genome and adaptive role for copy number variation in asexually propagated Solanum tuberosum
Open the record for dataset details and reuse information.
Auricular Malformations Driven by Copy Number Variations in a Hierarchical Enhancer Cluster and Dominant Enhancer Recapitulates Human Pathogenesis [PC-HiC]
GEO Series GSE263085. Homo sapiens. 1 samples. Type: Other.
Characterization of a new genetic signature associated with copy number variation that determines outcome in lung adenocarcinoma patients
GEO Series GSE197346. Homo sapiens. 40 samples. Type: Expression profiling by high throughput sequencing.
Copy number variation analysis of human Barrett's esophagus stem cells (HumanOmniZhongHua-8 v1.1 Beadchip)
GEO Series GSE68663. Homo sapiens. 53 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Single cell transcriptome analysis (scRNASeq) and inferred single cell copy number variations (scCNVs) of cancer associated fibroblast (CAFs) populations in murine KPC pancreatic tumors
GEO Series GSE180859. Mus musculus. 28 samples. Type: Expression profiling by high throughput sequencing.
Genomic copy number variation induced by TAQing system in Saccharomyces cerevisiae.
GEO Series GSE90025. Saccharomyces cerevisiae. 14 samples. Type: Genome variation profiling by genome tiling array.
Large scale copy number variation (CNV) at 14q12 is associated with the presence of genomic abnormalities in neoplasia.
GEO Series GSE4860. Homo sapiens. 8 samples. Type: Genome variation profiling by genome tiling array.
Clinically Relevant Copy Number Variations Detected in Cerebral Palsy
GEO Series GSE70374. Homo sapiens. 429 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 [AffymetrixCytoScanHD]
GEO Series GSE96897. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP array.
An initial map of chromosomal segmental copy number variations in chickens
GEO Series GSE19469. Gallus gallus. 10 samples. Type: Genome variation profiling by genome tiling array.
Subtypes of HPV-positive head and neck cancers are associated with HPV characteristics, copy number variations, PIK3CA mutation, and pathway signatures. [RNA-Seq]
GEO Series GSE74927. Homo sapiens. 36 samples. Type: Expression profiling by high throughput sequencing.
Quantitative analysis of chromatin interactions upon copy number variation at mouse 4E2 [RNA-seq]
GEO Series GSE64359. Mus musculus. 7 samples. Type: Expression profiling by high throughput sequencing.
Auricular Malformations Driven by Copy Number Variations in a Hierarchical Enhancer Cluster and Dominant Enhancer Recapitulates Human Pathogenesis
GEO Series GSE263087. Mus musculus. 3 samples. Type: Expression profiling by high throughput sequencing.
Copy number variation analysis of hepatic metastases from uveal melanoma
GEO Series GSE69614. Homo sapiens. 19 samples. Type: Genome variation profiling by SNP array.
Profiling of copy-number variation between BN and SHR rats
GEO Series GSE20102. Rattus norvegicus. 2 samples. Type: Genome variation profiling by genome tiling array.
A high resolution map of segmental DNA copy number variation in the mouse genome
GEO Series GSE5805. Mus musculus. 31 samples. Type: Genome variation profiling by genome tiling array.
wuHMM: a robust algorithm to detect DNA copy number variation using long oligonucleotide microarray data
GEO Series GSE10511. Mus musculus. 4 samples. Type: Genome variation profiling by genome tiling array.
Evaluation of copy number variation detection between high-resolution array CGH and low-coverage short-insert and mate-pair whole-genome sequencing
GEO Series GSE105092. Homo sapiens. 2 samples. Type: Genome variation profiling by array.
Copy number variation in inbred and wild mice
GEO Series GSE24424. Mus musculus; Mus spretus; Mus musculus domesticus. 64 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.