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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”
TREM2 Gene Dosage Increase Reprograms Microglia Responsivity and Ameliorates Pathological Phenotypes in Alzheimer’s Disease Models
GEO Series GSE104775. Mus musculus. 72 samples. Type: Expression profiling by high throughput sequencing.
Phenotypic manifestation of alpha-synuclein strains from Parkinson’s disease and multiple system atrophy in human dopaminergic neruons
GEO Series GSE149632. Homo sapiens. 24 samples. Type: Expression profiling by high throughput sequencing.
Fusion oncoproteins and cooperating mutations define disease phenotypes in NUP98-rearranged leukemia
GEO Series GSE287716. Homo sapiens. 13 samples. Type: Expression profiling by high throughput sequencing.
Ctla-4 deficiency induces an inflammatory bowel disease-like phenotype in a zebrafish model [scRNA-seq]
GEO Series GSE255303. Danio rerio. 2 samples. Type: Expression profiling by high throughput sequencing.
NBL1 Correlates with Renal Phenotypes in Mouse Models of Kidney Disease, but is not Causal: Male Mice with XLAS either HET or WT for Nbl1
GEO Series GSE310901. Mus musculus. 24 samples. Type: Expression profiling by high throughput sequencing.
Phenotypic heterogeneity driven by plasticity of the intermediate EMT state governs disease progression and metastasis in breast cancer [ATAC-seq]
GEO Series GSE172608. Homo sapiens. 14 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Delivery of A4GALT targeting siRNA-lipid nanoparticle rescues fabry disease phenotypes in hiPSC derived endothelial cell and podocyte models
GEO Series GSE282204. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
Phenotypic and genomic analysis of multiple myeloma minimal residual disease clonal plasma cells: a new model to understand chemoresistance [CytoScan750K Copy Number, LOH]
GEO Series GSE70397. Homo sapiens. 24 samples. Type: Genome variation profiling by SNP array.
The HDAC inhibitor 4b ameliorates the disease phenotype and transcriptional abnormalities in Huntington's disease transgenic mice
GEO Series GSE26317. Mus musculus. 47 samples. Type: Expression profiling by array.
Whole Genome DNA Methylation Analysis of Active Pulmonary Tuberculosis Disease Identifies Novel Epigenotypes: PARP9/miR-505/RASGRP4/GNG12 Gene Methylation and Clinical Phenotypes
GEO Series GSE118469. Homo sapiens. 21 samples. Type: Methylation profiling by array.
The TREM2-APOE pathway drives the transcriptional phenotype of dysfunctional microglia in neurodegenerative diseases IV
GEO Series GSE102562. Mus musculus. 20 samples. Type: Expression profiling by high throughput sequencing.
Characterisation of the sensory phenotype of the oesophageal mucosa in gastroesophageal reflux disease
GEO Series GSE226303. Homo sapiens. 46 samples. Type: Expression profiling by high throughput sequencing.
Mycobacterium avium ssp. paratuberculosis Infection Induces an Immune Tolerance Phenotype in Primary Bovine Macrophages from Johne’s Disease Cows (Agriculture and Agri-Food Canada_N.Bissonnette_J00007
GEO Series GSE98363. Bos taurus. 72 samples. Type: Expression profiling by high throughput sequencing.
HLA-B*46 associates with rapid HIV disease progression in Asian cohorts and prominent differences in NK cell phenotype
GEO Series GSE192384. Homo sapiens. 112 samples. Type: Expression profiling by high throughput sequencing.
Fusion oncoproteins and cooperating mutations define disease phenotypes in NUP98-rearranged leukemia [CUT&RUN]
GEO Series GSE287298. Homo sapiens. 98 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Novel human cellular model of CDA IV enables comprehensive analysis revealing molecular basis of disease phenotype.
GEO Series GSE226782. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Human microglia carrying an early-onset Parkinson’s disease mutation display cell-autonomous disease-relevant phenotypes that may worsen neuronal damage
GEO Series GSE241437. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
Modeling early phenotypes of Parkinson’s disease by age-induced midbrain-striatum assembloids
GEO Series GSE241632. Homo sapiens. 15 samples. Type: Expression profiling by high throughput sequencing.
Pro-inflammatory monocyte phenotype during acute progression of cerebral small vessel disease
GEO Series GSE162790. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Single-cell analysis identifies distinct macrophage phenotypes associated with pro-disease and pro-resolving functions in the endometriotic niche
GEO Series GSE274438. Mus musculus. 6 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.