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291
datasets available to search
ShareScore release 0.9.0
Dataset results
291 results for “Genetic variants”
Genome-wide maps of chromatin state (centromeric histone H3 variant CENP-A/Cnp1) in the meiotic progeny from the genetic crossing of mhf2∆ (cen1_inactive) × clr4∆ (cen1_active).
GEO Series GSE117960. Schizosaccharomyces pombe. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Genome-wide maps of chromatin state centromeric histone H3 variant CENP-A/Cnp1 in the meiotic progeny from the genetic crossings of mhf2+ (cen1_inactive) × mhf2+ (cen1_active) and mhf2∆ (cen1_inactive
GEO Series GSE131224. Schizosaccharomyces pombe. 22 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
PTEN variant and genetic backgrounds combine to modify cerebellar neuronal differentiation in autism spectrum disorder
GEO Series GSE310490. Homo sapiens. 9 samples. Type: Expression 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 [captureC]
GEO Series GSE272080. Homo sapiens. 6 samples. Type: Other.
Promoter sequence and architecture determine expression variability and confer robustness to genetic variants [immortalized lymphoblastoid cell lines]
GEO Series GSE188130. Homo sapiens. 108 samples. Type: Expression 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 [HiC]
GEO Series GSE272172. Homo sapiens. 3 samples. Type: Other.
Multiplexed functional assessment of dominant genetic variants in CARD11
GEO Series GSE152129. Homo sapiens. 147 samples. Type: Other; Genome variation profiling by high throughput sequencing.
Genetic Variants in Egyptian Patients Receiving HCQ(Hydroxychloroquine)
ClinicalTrials.gov study NCT03180190. IPD Sharing: NO. Countries: 0. Publications: 0.
Clotting Genetic Variants, Hormones, and Venous Thrombosis
ClinicalTrials.gov study NCT00094185. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Effectiveness of Muscular Work and Genetic Variants in Strength Gain of Ischiofemoral and Quadriceps
ClinicalTrials.gov study NCT03973060. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Interaction of Potassium and Genetic Risk Variants on Diabetes Risk
ClinicalTrials.gov study NCT03367455. IPD Sharing: NO. Countries: 0. Publications: 0.
A Single Center Prospective Study in an Estimated 570 Patients Who Underwent Genetic Screening at UZ Brussel in the Context of a Primary Cardiac Arrhythmia. Patients Showing a Variant Class 3,4 or 5 i
ClinicalTrials.gov study NCT07183059. IPD Sharing: UNDECIDED. Countries: 0. Publications: 0.
Massively parallel analysis of genotype-dependent enhancer activity among atopic dermatitis genetic risk variants
GEO Series GSE300756. Homo sapiens. 6 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Genetic variants in Major Histocompatibility Complex-linked genes Associate with Pediatric Liver Transplant Rejection
GEO Series GSE11361. Homo sapiens. 52 samples. Type: Expression profiling by array.
Functional Validation of Common Idiopathic Pulmonary Fibrosis Genetic Risk Variants
GEO Series GSE175459. Homo sapiens. 969 samples. Type: Expression profiling by high throughput sequencing; Methylation profiling by genome tiling array.
Neutrophils restricted contribution of CCRL2 genetic variants to COVID-19 severity
GEO Series GSE269643. Homo sapiens. 12 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Genetic variants affecting RNA stability influence complex traits and disease risk II
GEO Series GSE298114. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Functional characterization of Alzheimer´s disease genetic variants in microglia
GEO Series GSE206478. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Control iPSC lines with clinically annotated genetic variants for versatile multi-lineage differentiation
GEO Series GSE132012. Homo sapiens. 4 samples. Type: Other.
Unique DNA methylation signature may not specifically characterize BLBS across distinct genetic variants
GEO Series GSE281737. Homo sapiens. 52 samples. Type: Methylation profiling by genome tiling array.
ScienceDex guides
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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.