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 Study Assessing the Safety and Efficacy of Multiple Intravitreal KH902 in Patients With CNV Due to AMD
ClinicalTrials.gov study NCT01242254. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Study of the Intravitreal Implantation of NT-503-3 Encapsulated Cell Technology (ECT) for the Treatment of Recurrent Choroidal Neovascularization (CNV) Secondary to Age-related Macular Degeneration (A
ClinicalTrials.gov study NCT02228304. IPD Sharing: Not stated. Countries: 2. Publications: 0.
Comparison Between Foresee Home and Optical Coherence Tomography (OCT) Visual Field Defects in Patients With Choroidal Neovascularization (CNV)
ClinicalTrials.gov study NCT01073592. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Does Vascular Endothelial Growth Factor (VEGF) or Complement Factor H Gene Polymorphism Play a Role in the Treatment Success With VEGF Inhibitors in Patients With Choroidal NeoVascularization (CNV)?
ClinicalTrials.gov study NCT00813514. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Time Course of Activity Signs at SD-OCT High Frequency Intravitreal Ranibizumab Treatment in CNV Due to AMD
ClinicalTrials.gov study NCT03393767. IPD Sharing: Not stated. Countries: 1. Publications: 0.
High-density genome-wide copy number variation (CNV) in human head and neck paragangliomas.
GEO Series GSE49614. Homo sapiens. 51 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
CNV analysis of 140 Filipinos with Cleft Lip and/or Palate
GEO Series GSE100845. Homo sapiens. 140 samples. Type: Genome variation profiling by genome tiling array.
Oligo array for CNV calling AUTS2 project [Agilent]
GEO Series GSE37141. Homo sapiens. 2 samples. Type: Genome variation profiling by genome tiling array.
Trunk events present minimal intra- and inter-tumoral heterogeneity in hepatocellular carcinoma [multinodular CNV]
GEO Series GSE98618. Homo sapiens. 56 samples. Type: Genome variation profiling by SNP array.
Modulation of global expression by aneuploids and CNV of dosage sensitive regulatory genes
GEO Series GSE180089. Drosophila melanogaster. 4 samples. Type: Expression profiling by high throughput sequencing.
Affymetrix SNP and CNV data for the HuRef individual
GEO Series GSE20275. Homo sapiens. 1 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.
NanoString DNA data for CNV Analysis
GEO Series GSE99355. Homo sapiens. 65 samples. Type: Genome variation profiling by array.
Oligo array for calling CNV's for AUTS2 project [NimbleGen]
GEO Series GSE37654. Homo sapiens. 1 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.
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.
CNV analysis of 233 individuals of European ancestry and 6 individuals of non-European ancestry with cleft lip and/or cleft palate
GEO Series GSE212165. Homo sapiens. 239 samples. Type: Genome variation profiling by genome tiling array.
OncoScan™ CNV FFPE Assay data for desmoid tumors
GEO Series GSE250149. Homo sapiens. 23 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
7q11.23 CNV alters ribosomal biogenesis, mTOR and neuronal intrinsic excitability [RNA-seq]
GEO Series GSE261691. Homo sapiens. 24 samples. Type: Expression profiling by high throughput sequencing.
CNV Polymorphisms Modulate the Expression of GST Subtypes in the Human Small Airway Epithelium and Alveolar Macrophages
GEO Series GSE20250. Homo sapiens. 211 samples. Type: Expression profiling by array; Genome variation profiling by SNP array.
SNP array for CNV calling AUTS2 project [Affymetrix]
GEO Series GSE36950. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP 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.