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291
datasets available to search
ShareScore release 0.9.0
Dataset results
291 results for “Genetic variants”
Genetic effects on liver chromatin accessibility identify disease regulatory variants
GEO Series GSE164942. Homo sapiens. 60 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Genome variation profiling by SNP array.
Addiction-associated genetic variants implicate brain cell type- and region-specific cis-regulatory elements in addiction neurobiology
GEO Series GSE161374. Mus musculus. 35 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Allele-Specific Methylation Occurs at Genetic Variants Associated with Complex Disease
GEO Series GSE56298. Homo sapiens. 82 samples. Type: Methylation profiling by high throughput sequencing.
Discriminating activities of DEAD-Box Helicase 41 from myeloid malignancy-associated germline variants by genetic rescue
GEO Series GSE208400. Mus musculus. 15 samples. Type: Expression profiling by high throughput sequencing.
U937 cells with CRISPR interference at regulatory genetic variants [4C-seq]
GEO Series GSE281909. Homo sapiens. 6 samples. Type: Other.
Promoter sequence and architecture determine expression variability and confer robustness to genetic variants
GEO Series GSE188131. Homo sapiens. 116 samples. Type: Expression profiling by high throughput sequencing.
CRISPR gene editing, cardiac disease modelling and transcriptomics interpretation of a novel GATA4 patient genetic variant
GEO Series GSE229879. Homo sapiens. 26 samples. Type: Expression profiling by high throughput sequencing; Other.
Functional characterization of Alzheimer´s disease genetic variants in microglia
GEO Series GSE206480. Homo sapiens. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Oxygen tension modulates the mitochondrial genetic bottleneck and influences the segregation of a heteroplasmic mtDNA variant
GEO Series GSE169427. Mus musculus. 768 samples. Type: Expression profiling by high throughput sequencing.
Classifying pathogenic variants in amyloid beta using intramolecular genetic interaction profiling
GEO Series GSE247583. Saccharomyces cerevisiae. 6 samples. Type: Other.
Genetic Variants of Phospholipase C-γ2 Confer Altered Microglial Phenotypes and Differential Risk for Alzheimer’s Disease
GEO Series GSE239658. Mus musculus. 72 samples. Type: Expression profiling by high throughput sequencing; Other.
Expression of long non-coding RNAs in autoimmunity and linkage to enhancer function and autoimmune disease risk genetic variants
GEO Series GSE92472. Homo sapiens. 15 samples. Type: Expression profiling by high throughput sequencing.
Identification of Common Genetic Variants that Account for Transcript Isoform Variation between Human Populations
GEO Series GSE9703. Homo sapiens. 176 samples. Type: Expression profiling by array.
A genetic variant controls interferon-β gene expression in human myeloid cells by preventing C/EBP-β binding on a conserved enhancer
GEO Series GSE137514. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Genetic effects on liver chromatin accessibility identify disease regulatory variants [genotypes]
GEO Series GSE164938. Homo sapiens. 20 samples. Type: Genome variation profiling by SNP array.
Transcriptional profiling of striatum from the Q140 mouse model of Huntington's disease, from A rare genetic variant confers resistance to neurodegeneration across multiple neurological disorders by a
GEO Series GSE281823. Mus musculus. 40 samples. Type: Expression profiling by high throughput sequencing.
Integrative functional genomic analyses identify genetic variants influencing skin pigmentation in Africans [HiChIP & Hi-C]
GEO Series GSE248849. Homo sapiens. 8 samples. Type: Other.
Non-coding genetic variants dominant in African American reveal prostate cancer risk
GEO Series GSE276748. Homo sapiens. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Functional characterization of Alzheimer´s disease genetic variants in microglia
GEO Series GSE206479. Homo sapiens. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
3D chromatin-based variant-to-gene maps across 57 human cell types reveal the cellular and genetic architecture of autoimmune disease susceptibility [ATAC-seq]
GEO Series GSE272120. Homo sapiens. 14 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.