Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
270
datasets available to search
ShareScore release 0.9.0
Dataset results
270 results for “Disease Phenotypes”
Integrated Genetic and Epigenetic Analysis of Childhood ALL Reveals a Synergistic Role for Structural and Epigenetic Lesions In Determining Disease Phenotype
GEO Series GSE44862. Homo sapiens. 380 samples. Type: Methylation profiling by genome tiling array.
Monozygotic twins discordant for recessive dystrophic epidermolysis bullosa phenotype highlight the role of TGF-β signalling in modifying disease severity
GEO Series GSE51056. Homo sapiens. 8 samples. Type: Expression profiling by array.
Phenotypic heterogeneity driven by plasticity of the intermediate EMT state governs disease progression and metastasis in breast cancer
GEO Series GSE172613. Homo sapiens. 35 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
Integrated Genetic and Epigenetic Analysis of Childhood Acute Lymphoblastic Leukemia Reveals a Synergistic Role for Structural and Epigenetic Lesions In Determining Disease Phenotype
GEO Series GSE26281. Homo sapiens. 154 samples. Type: Expression profiling by array.
Triplication of HSA21-encoded genes modulates Alzheimer's Disease-related phenotypes in vivo via interferon signaling
GEO Series GSE272851. Mus musculus. 136 samples. Type: Expression profiling by high throughput sequencing; Other.
GENETIC CORRECTION OF HUNTINGTON'S DISEASE PHENOTYPES IN INDUCED PLURIPOTENT STEM CELLS
GEO Series GSE37547. Homo sapiens. 16 samples. Type: Expression profiling by array.
Depletion of p62 reduces nuclear inclusions and paradoxically ameliorates disease phenotypes in Huntington’s model mice
GEO Series GSE62210. Mus musculus. 12 samples. Type: Expression profiling by array.
Integrated Genetic and Epigenetic Analysis of Childhood ALL Reveals a Synergistic Role for Structural and Epigenetic Lesions In Determining Disease Phenotype [194 samples]
GEO Series GSE44860. Homo sapiens. 194 samples. Type: Methylation profiling by genome tiling array.
Phenotypic heterogeneity driven by plasticity of the intermediate EMT state governs disease progression and metastasis in breast cancer [RNA-seq]
GEO Series GSE172609. Homo sapiens. 21 samples. Type: Expression profiling by high throughput sequencing.
Genomic and Phenotypic Evidence for a Causative Role of Calcineurin in the Astrogliosis of Aging and Alzheimer's Disease
GEO Series GSE1978. Rattus norvegicus. 23 samples. Type: Expression profiling by array.
Genetically programmed alternative splicing of NEMO mediates an autoinflammatory disease phenotype
GEO Series GSE196243. Homo sapiens. 257 samples. Type: Expression profiling by high throughput sequencing.
The TREM2-APOE pathway drives the transcriptional phenotype of dysfunctional microglia in neurodegenerative diseases
GEO Series GSE101689. Mus musculus. 246 samples. Type: Expression profiling by array; Expression profiling by high throughput sequencing.
Whole blood transcriptomics characterize molecular phenotypes of pulmonary Mycobacterium avium complex disease
GEO Series GSE288604. Homo sapiens. 200 samples. Type: Expression profiling by high throughput sequencing.
Fusion oncoproteins and cooperating mutations define disease phenotypes in NUP98-rearranged leukemia [RNA-seq]
GEO Series GSE287297. Homo sapiens. 70 samples. Type: Expression profiling by high throughput sequencing.
Dataset related to article "Emerging Variants, Unique Phenotypes, and Transcriptomic Signatures in COASY-Associated Diseases"
<p>The database contains the raw data included in the article at title.</p>
Prediction of Amyloid and Mild Cognitive Impairment in Early Stage Alzheimer's Disease From Remote Speech Phenotyping
ClinicalTrials.gov study NCT04928690. IPD Sharing: UNDECIDED. Countries: 0. Publications: 0.
Integrated Phenotyping of the Gut-plAtelet-Liver AXIS in the Progression of Chronic Liver Disease (iGAL-AXIS)
ClinicalTrials.gov study NCT06623084. IPD Sharing: NO. Countries: 0. Publications: 0.
Myocardial Affectation in Patients With Fabry Disease Without Phenotypic Manifestation. Diagnostic Value of Biomarkers
ClinicalTrials.gov study NCT01442350. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Clinical, Radiological, Tissue and Biological Phenotyping for the Analysis of the Transition From Physiology to Pathology in Pulmonary Diseases With Pulmonary Hypertension
ClinicalTrials.gov study NCT07184671. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Phenotypic and genomic analysis of multiple myeloma minimal residual disease clonal plasma cells: a new model to understand chemoresistance [HuGene-1_0 Expression]
GEO Series GSE70398. Homo sapiens. 14 samples. Type: Expression profiling by 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.