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Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
83
datasets available to search
ShareScore release 0.9.0
Dataset results
83 results for “SNP analysis”
Structural genomic variation analysis in patients with bone marrow failure using Illumina Infinium SNP Arrays
GEO Series GSE48484. Homo sapiens. 122 samples. Type: SNP genotyping by SNP array.
Copy number variation analysis in Japanese children with Autsim Spectrum Disorder by Affymetrix Genome-Wide Human SNP Array 6.0.
GEO Series GSE144918. Homo sapiens. 192 samples. Type: Genome variation profiling by SNP array.
Combined arrayCGH and SNP-loss of heterozygosity analysis in cervical cancer
GEO Series GSE8605. Homo sapiens. 40 samples. Type: Expression profiling by array; Genome variation profiling by genome tiling array; Genome variation profiling by SNP array; SNP genotyping by SNP array.
SNP Analysis of Primary Glioblastoma Cell Lines
GEO Series GSE5082. Homo sapiens. 5 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
High Resolution Copy Number Analysis of Paraffin Embedded Archival Tissue Using SNP BeadArrays
GEO Series GSE5347. Homo sapiens. 63 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
SNP array analysis of chromosomal instability patterns discriminates rectal adenomas from carcinomas
GEO Series GSE7946. Homo sapiens. 97 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Characterization of genomic imbalances in diffuse large B-cell lymphoma by high resolution SNP-chip analysis
GEO Series GSE57612. Homo sapiens. 296 samples. Type: Expression profiling by array; Genome variation profiling by SNP array; SNP genotyping by SNP array.
Affymetrix SNP array data for longitudinal analysis of adult Myelodysplastic Syndromes (MDS) and Acute Myeloid Leukemia (AML) with 1q jumping translocation after 5'-azacytidine treatment
GEO Series GSE272012. Homo sapiens. 7 samples. Type: Genome variation profiling by genome tiling array; Genome variation profiling by SNP array.
Comparison of primary neuroblastoma tumors and derivative early-passage cell lines using genome-wide SNP array analysis
GEO Series GSE14656. Homo sapiens. 54 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
SNP array analysis of neuroblastic tumor NB99
GEO Series GSE12461. Homo sapiens. 1 samples. Type: Genome variation profiling by SNP array.
eQTL Analysis Identifies Novel Associations Between Genotype and Gene Expression in the Human Intestine (Illumina SNP)
GEO Series GSE41238. Homo sapiens. 173 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Mesothelioma cell lines SNP data copy number analysis
GEO Series GSE29383. Homo sapiens. 25 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Chromophobe and Oncocytoma Renal Cell Carcinomas: gene expression and SNP analysis
GEO Series GSE8271. Homo sapiens. 34 samples. Type: Expression profiling by array; Genome variation profiling by SNP array; SNP genotyping by SNP array.
Affymetrix SNP 6.0 data for analysis of esophageal adenocarcinoma samples
GEO Series GSE49396. Homo sapiens. 82 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
SNP analysis AID-low vs AID-high
GEO Series GSE13612. Homo sapiens. 23 samples. Type: Genome variation profiling by SNP array.
SNP genotyping of cryptic complexity in structural chromosome abnormalities previously detected by cytogenetic analysis
GEO Series GSE20623. Homo sapiens. 40 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Detailed genome-wide SNP analysis of major salivary carcinomas localizes subtype-specific chromosome sites and oncogenes of potential clinical significance
GEO Series GSE44434. Homo sapiens. 76 samples. Type: Genome variation profiling by SNP array.
SNP microarry analysis of primary and first recurrent pediatric ependymoma
GEO Series GSE50876. Homo sapiens. 29 samples. Type: Genome variation profiling by SNP array.
Development of molecular markers linked to powdery mildew resistance gene Pm4b by combining SNP discovery from transcriptome sequencing data with bulked segretant analysis (BSR-seq) in wheat
GEO Series GSE108697. Triticum aestivum. 2 samples. Type: Genome variation profiling by high throughput sequencing.
SNP array analysis on Maffucci tumours
GEO Series GSE26674. Homo sapiens. 7 samples. Type: Genome variation profiling by SNP array; SNP genotyping 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.