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2,880
datasets available to search
ShareScore release 0.9.0
Dataset results
2,880 results for “variant”
SMCHD1 variants induce variegated expression in Facio Scapulo Humeral Dystrophy and Bosma Arhinia and microphtalmia syndrome (Methylation).
GEO Series GSE175527. Homo sapiens. 28 samples. Type: Methylation profiling by array.
A homologous or variant booster vaccine after Ad26.COV2.S immunization enhances SARS-CoV-2-specific immune responses in rhesus macaques
GEO Series GSE193264. Macaca mulatta. 50 samples. Type: Expression profiling by high throughput sequencing.
Identification and characterization of androgen receptor splice variants preferred bindings that drive prostate cancer progression
GEO Series GSE80743. Homo sapiens. 29 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Connecting cilium, stress response and proteostasis abnormalities inform variant and therapy assessment in RPGRIP1 retinal organoids [RNA-Seq]
GEO Series GSE293982. Homo sapiens. 9 samples. Type: Expression profiling by high throughput sequencing.
Antitumor immunity induced by antibody-based natural killer cell engager therapeutics armed with not-alpha IL-2 variant
GEO Series GSE214378. Homo sapiens. 30 samples. Type: Expression profiling by high throughput sequencing.
Expression data from the seed coats of black (iRT) and brown (irT) soybean variant for alleles of the R locus
GEO Series GSE26208. Glycine max. 6 samples. Type: Expression profiling by array.
Variants in ZFX Cause an X-linked Neurodevelopmental Disorder with Recurrent Facial Gestalt
GEO Series GSE218688. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
Identification of introduced and stably inherited DNA methylation variants in soybean associated with soybean cyst nematode parasitism [RNA-seq]
GEO Series GSE130138. Glycine max. 12 samples. Type: Expression profiling by high throughput sequencing.
Novel risk variants affecting enhancers of TH1 and TREG cells in type 1 diabetes [ChIP-seq]
GEO Series GSE112337. Homo sapiens. 66 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Identification of a Therapeutically Targetable JAK-STAT Enriched Androgen Receptor (AR) and AR Splice Variant Positive Triple Negative Breast Cancer Subtype [MDA-MB-453]
GEO Series GSE245554. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Genetic effects on liver chromatin accessibility identify disease regulatory variants [RNA-seq]
GEO Series GSE164876. Homo sapiens. 20 samples. Type: Expression profiling by high throughput sequencing.
Histone variant, H2B.Z demarcates the AT-rich promoter regions of the Plasmodium falciparum genome
GEO Series GSE39702. Plasmodium falciparum 3D7. 6 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Multi-omic comparison of Alzheimer’s variants in human ESC-derived microglia reveals convergence at APOE
GEO Series GSE153658. Homo sapiens. 103 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Massively parallel reporter assays combined with cell-type specific eQTL identified a functional melanoma risk variant in HIV-1 restriction gene, MX2
GEO Series GSE129250. Homo sapiens. 61 samples. Type: Expression profiling by high throughput sequencing; Other.
Pleomorphic Variants of Borreliella (syn. Borrelia) burgdorferi Express Evolutionary Distinct Transcriptomes
GEO Series GSE199941. Borreliella burgdorferi. 11 samples. Type: Expression profiling by high throughput sequencing.
SARS-CoV-2 spike P681R mutation, a hallmark of the Delta variant, enhances viral fusogenicity and pathogenicity
GEO Series GSE182738. Severe acute respiratory syndrome coronavirus 2. 6 samples. Type: Genome variation profiling by high throughput sequencing.
Effects of coronary artery disease-associated variants on vascular smooth muscle cells
GEO Series GSE189300. Homo sapiens. 1499 samples. Type: Expression profiling by high throughput sequencing.
New strategies for the identification of intronic variants related to splicing events in pancreas cancer [iCELL8]
GEO Series GSE229006. Homo sapiens. 10 samples. Type: Expression profiling by high throughput sequencing.
LRRK2 G2019S variant triggers transcriptional changes in Parkinson’s disease human myeloid cells under pro-inflammatory environment
GEO Series GSE240907. Homo sapiens. 27 samples. Type: Expression profiling by high throughput sequencing.
Next-generation RNA sequencing of human astrocyte cultures to study the comparative levels of transmembrane proteins and their transcriptional variants
GEO Series GSE228084. Homo sapiens. 4 samples. Type: Expression 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.