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320
datasets available to search
ShareScore release 0.9.0
Dataset results
320 results for “SNP array”
Genome-wide analysis in Human Colorectal Cells reveals Ischaemia-mediated expression of motility genes via DNA hypomethylation (SNP array)
GEO Series GSE58232. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP array.
Affymetrix SNP array data for oral squamous cell carcinoma
GEO Series GSE25103. Homo sapiens. 122 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
(SNP Array) Single-Cell Multi-Omics Identifies Chronic Inflammation as a Driver of TP53 mutant Leukaemic Evolution
<p>Single nucleotide polymorphism (SNP) array data files related our publication titled "Single-Cell Multi-Omics Identifies Chronic Inflammation as a Driver of <em>TP53 </em>mutant Leukaemic Evolution".</p>
Genome Wide SNP Array-based Approach to Detect Micro-cytogenetic Lesions and KIT Mutation to Improve Treatment Outcomes in Patients With Core-binding Factor Positive Acute Myeloid Leukemia
ClinicalTrials.gov study NCT01066286. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Genome-wide Pharmacogenetic Candidate Gene Single Nucleotide Polymorphism (SNP) Array-based Approach to Predict Chemoresponse and Survival in Patients With Acute Myeloid Leukemia With Normal Karyotype
ClinicalTrials.gov study NCT01066338. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Genome-wide Single Nucleotide Polymorphism (SNP) Array-based Approach to Predict Chemoresponse and Survival in Patients With Acute Lymphoblastic Leukemia
ClinicalTrials.gov study NCT01079507. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Prenatal Molecular Characterisation by CGH+SNP-ARRAY of Supernumerary Marker Chromosomes and de Novo Apparently Balanced Reciprocal Translocations
ClinicalTrials.gov study NCT01907425. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Illumina SNP array data for Brugdata syndrome patients in Taiwan
GEO Series GSE46348. Homo sapiens. 16 samples. Type: Genome variation profiling by SNP array.
Illumina SNP array data for acute myeloid leukemia samples
GEO Series GSE95690. Homo sapiens. 412 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Whole genome SNP array of 16 look-alike human couples
GEO Series GSE142300. Homo sapiens. 32 samples. Type: SNP genotyping by SNP array.
Affymetrix SNP array data for esophageal squamous cell carcinoma samples
GEO Series GSE59105. Homo sapiens. 162 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.
Whole genome SNP array data from myelodysplastic syndromes (MDS) patients
GEO Series GSE57229. Homo sapiens. 14 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses [murine SNP array]
GEO Series GSE107510. Mus musculus. 12 samples. Type: Genome variation profiling by SNP array.
Affymetrix OncoScan SNP arrays for profiling somatic copy-number alterations in blastic plasmacytoid dendritic cell neoplasm
GEO Series GSE200113. Homo sapiens. 45 samples. Type: Genome variation profiling by array; Genome variation profiling by SNP array.
Affymetrix SNP 250K array data for paediatric high grade gliomas
GEO Series GSE59678. Homo sapiens. 35 samples. Type: SNP genotyping by SNP array.
Affymetrix 6.0 SNP arrays interrogated to detect allele-specific DNA modification in the brain
GEO Series GSE71443. Homo sapiens. 230 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array; Methylation profiling by SNP array.
Affymetrix SNP array data for B-lineage acute lymphoblastic leukemia
GEO Series GSE67405. Homo sapiens. 25 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.
Derivation and differentiation of haploid human embryonic stem cells [SNP array]
GEO Series GSE74950. Homo sapiens. 4 samples. Type: Genome variation profiling by SNP array.
Affymetrix SNP array data for dog OCD samples
GEO Series GSE53488. Canis lupus familiaris. 176 samples. Type: SNP genotyping by SNP array.
Karyotyping using SNP array of primary uveal melanoma cells, normal uveal melanocytes, neural crest stem cells, embryonic stem cells and uveal melanoma cell lines MUM2B and OCM1A
GEO Series GSE44297. Homo sapiens. 63 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.