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1,023
datasets available to search
ShareScore release 0.9.0
Dataset results
1,023 results for “copy number”
Micro-scale genomic copy number aberrations as another means of mutagenesis in breast cancer
GEO Series GSE36889. Homo sapiens. 192 samples. Type: Genome variation profiling by array; Genome variation profiling by genome tiling array.
Copy number profiling of 92 human lung tumors on Affymetrix 100K SNP arrays
GEO Series GSE39793. Homo sapiens. 184 samples. Type: Genome variation profiling by SNP array.
Integrative analysis reveals relationships of genetic and epigenetic alterations in osteosarcoma [DNA copy number]
GEO Series GSE36003. Homo sapiens. 19 samples. Type: Genome variation profiling by SNP array.
FFPE study using MIP copy number platform - breast cancer II
GEO Series GSE14744. Homo sapiens. 56 samples. Type: Genome variation profiling by SNP array.
A High-Resolution Copy Number Variation Resource for Clinical Genetics
GEO Series GSE59150. Homo sapiens. 873 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array; Genome variation profiling by genome tiling array.
Quantification of Normal Cell Fraction and Copy Number Neutral LOH in Clinical Lung Cancer Samples Using SNP Array Data
GEO Series GSE16092. Homo sapiens. 50 samples. Type: Genome variation profiling by SNP array.
Integrative analysis of gene expression profiling and genomic copy number in Gastrointestinal Stromal Tumors
GEO Series GSE20710. Homo sapiens. 47 samples. Type: Expression profiling by array; Genome variation profiling by SNP array.
DNA copy number profiling of lung adenocarcinomas and patient-matched non-malignant lung
GEO Series GSE139294. Homo sapiens. 166 samples. Type: Genome variation profiling by SNP array.
SNP arrays to detect copy number changes in t(1;19) E2A-PBX1 positive leukemias
GEO Series GSE52654. Homo sapiens. 21 samples. Type: Genome variation profiling by genome tiling array.
Somatic mosaicism for copy number variation in differentiated human tissues
GEO Series GSE9598. Homo sapiens. 74 samples. Type: Genome variation profiling by genome tiling array.
Integrative analysis of copy number and gene expression data suggests novel pathogenic mechanisms in Primary Myelofibrosis
GEO Series GSE69161. Homo sapiens. 31 samples. Type: Genome variation profiling by genome tiling array; Genome variation profiling by SNP array; SNP genotyping by SNP array.
Gene Copy Number Aberrations are Associated with Survival in Histological Subgroups of Non-Small Cell Lung Cancer
GEO Series GSE28582. Homo sapiens. 201 samples. Type: Expression profiling by array; Genome variation profiling by SNP array.
Copy-number profiling by SNP array of 4 acute myeloid leukemia (AML) cell lines
GEO Series GSE138438. Homo sapiens. 4 samples. Type: Genome variation profiling by SNP array.
Integration of transcript expression, copy number and LOH analysis of infiltrating ductal carcinoma of the breast: expression analysis
GEO Series GSE22544. Homo sapiens. 20 samples. Type: Expression profiling by array.
Stratification of clear cell renal cell carcinoma (ccRCC) genomes by gene-directed copy number alteration (CNA) analysis
GEO Series GSE95239. Homo sapiens. 48 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Auricular Malformations Driven by Copy Number Variations in a Hierarchical Enhancer Cluster and Dominant Enhancer Recapitulates Human Pathogenesis [CUT&RUN]
GEO Series GSE263084. Homo sapiens. 6 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
FFPE study using MIP copy number platform - liver
GEO Series GSE14745. Homo sapiens. 38 samples. Type: Genome variation profiling by SNP array.
Copy number variation in the bovine genome
GEO Series GSE18174. Bos taurus. 114 samples. Type: Genome variation profiling by genome tiling array.
Integrated copy number and expression analysis identifies profiles of whole-arm chromosomal alterations and subgroups with favorable outcome in ovarian clear cell carcinomas
GEO Series GSE65986. Homo sapiens. 55 samples. Type: Expression profiling by array.
Isw2 and Ino80 chromatin remodeling factors regulate chromatin, replication, and copy number at the yeast ribosomal DNA locus
GEO Series GSE112465. Saccharomyces cerevisiae. 63 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
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.