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281
datasets available to search
ShareScore release 0.9.0
Dataset results
281 results for “copy number variation”
Copy Number Variation of human hepatocellular carcinoma (HCC) and Cholangiocarcinoma (CCA) from the Thailand Initiative in Genomics and Expression Research for Liver Cancer (TIGER-LC)
GEO Series GSE76213. Homo sapiens. 304 samples. Type: Genome variation profiling by SNP array.
Evaluation of affinity-based genome-wide DNA methylation data: effects of CpG density, amplification bias and copy number variation
GEO Series GSE24546. Homo sapiens. 40 samples. Type: Methylation profiling by genome tiling array; Methylation profiling by high throughput sequencing; Genome variation profiling by SNP array.
Genomic copy number variations in the genomes of leukocytes predict prostate cancer clinical outcomes
GEO Series GSE70650. Homo sapiens. 273 samples. Type: Genome variation profiling by SNP array.
High-resolution map of copy number variations in motor cortex of Control and Sporadic Amyotrphic Lateral Sclerosis patients by using a customized exon-centric comparative genomic hybridization array.
GEO Series GSE107375. Homo sapiens. 40 samples. Type: Genome variation profiling by array.
A Family Study of Copy Number Variations in Patients With Autism Spectrum Disorder
ClinicalTrials.gov study NCT02228876. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Investigation of the HDAC4 Copy Number Variation and Its Effect on Gene and Protein Expression in Patients With ASD
ClinicalTrials.gov study NCT03670381. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Study of DNA Copy Numbers Variations and Gene Expression Profile of Bone Marrow Plasma Cells From MGUS and SMM.
ClinicalTrials.gov study NCT01079429. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Investigation of Copy Number Variations and Genetic Variants in POI
ClinicalTrials.gov study NCT05327283. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Development of a NIPTT for Detecting Copy Number Variations
ClinicalTrials.gov study NCT04774640. IPD Sharing: NO. Countries: 1. Publications: 0.
Copy Number Variation in Prenatal Diagnosis
ClinicalTrials.gov study NCT04561440. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Association of Copy Number Variations in the SMN Genes With Acute Kidney Injury After Heart Surgery
ClinicalTrials.gov study NCT04317196. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Copy Number Variation in CHRNA7 Gene in Migraine and Gene Expression
ClinicalTrials.gov study NCT04912752. IPD Sharing: NO. Countries: 1. Publications: 0.
Copy Number Variations, Inflammatory Cytokines and the Risk of Dementia
ClinicalTrials.gov study NCT00878280. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Copy number variation profiling of gastric tissues: Cancer Samples vs. Matched Adjacent Noncancerous Samples
GEO Series GSE33428. Homo sapiens. 27 samples. Type: Genome variation profiling by genome tiling array.
Genome-wide analysis of gene expression and DNA copy number variations in small cell esophageal carcinoma
GEO Series GSE111299. Homo sapiens. 9 samples. Type: Expression profiling by array; Genome variation profiling by genome tiling array.
High copy number variation burdens in cranial meningiomas from patients with diverse clinical phenotypes characterized by hot genomic structure changes
GEO Series GSE147673. Homo sapiens. 383 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.
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.
De novo copy number variations in cloned dogs (Illumina SNP)
GEO Series GSE49123. Canis lupus familiaris. 8 samples. Type: SNP genotyping by SNP array.
Global variation of copy number in the human genome_EA
GEO Series GSE5013. Homo sapiens. 612 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Copy Number Variation across 12 tribes of African cichlid species
GEO Series GSE117914. Cyathopharynx furcifer; Oreochromis alcalicus; Pseudocrenilabrus multicolor victoriae; Cyprichromis leptosoma; Labeotropheus fuelleborni; Oreochromis ndalalani; Astatotilapia flaviijosephi; Xenotilapia spiloptera; Julidochromis ornatus; Rhamphochromis longiceps; Coptodon fusiforme; Coptodon kottae; Sarotherodon lamprechti; Lobochilotes labiata; Sarotherodon galilaeus; Tropheus moorii; Haplochromis burtoni; Ophthalmotilapia ventralis; Boulengerochromis microlepis; Neolamprologus brichardi; Eretmodus cyanostictus; Hemichromis fasciatus; Stomatepia mariae; Copadichromis virginalis; Diplotaxodon greenwoodi; Pallidochromis tokolosh; Konia eisentrauti; Benthodesmus elongatus; Coptodon zillii; Cyphotilapia frontosa; Lepidiolamprologus elongatus; Sarotherodon melanotheron; Oreochromis grahami; Pungu maclareni; Nyassachromis microcephalus; Tropheops sp. 'red cheek'; Haplochromis thereuterion; Coptodon deckerti; Oreochromis niloticus; Astatotilapia calliptera; Callochromis
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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.