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.
376
datasets available to search
ShareScore release 0.9.0
Dataset results
376 results for “Causality”
Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3’ UTR of FAIM2 (snRNA-Seq)
GEO Series GSE241594. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Human and rat skeletal muscle single-nuclei multi-omic integrative analyses nominate causal cell types, regulatory elements, and SNPs for complex traits [snRNA-seq]
GEO Series GSE178734. Rattus norvegicus; Homo sapiens. 7 samples. Type: Expression profiling by high throughput sequencing.
Coupled single-cell epigenome editing and profiling reveals causal gene regulatory networks [Bulk ATAC-seq]
GEO Series GSE116247. Homo sapiens. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
TDP-43, an ALS/FTD causal gene, regulates SREBF2-mediated cholesterol metabolism in the CNS
GEO Series GSE133047. Mus musculus. 21 samples. Type: Expression profiling by high throughput sequencing.
Genome-wide enhancer-gene regulatory maps link causal variants to target genes underlying human colorectal cancer risk [RNA-seq]
GEO Series GSE222769. Homo sapiens. 10 samples. Type: Expression profiling by high throughput sequencing.
Assessing the ability of various genomic features to prioritize causal non-coding variants associated with diseases and traits [CRISPR guide-seq]
GEO Series GSE136693. Homo sapiens. 168 samples. Type: Other.
Multiple causal variants underlie genetic associations in humans
GEO Series GSE174534. synthetic construct; Homo sapiens. 7 samples. Type: Expression profiling by high throughput sequencing; Other.
Genetic landscape and functional exploration of kidney cancer predisposition causality in cross-ancestral populations
GEO Series GSE279473. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
RNA-Seq analysis of maize lines resistant and susceptible to Cercospora zeina, causal organism of Grey leafspot disease
GEO Series GSE99005. Zea mays. 6 samples. Type: Expression profiling by high throughput sequencing.
Causal linkage of presence of mutant NPM1 to efficacy of novel therapeutic agents against AML cells with mutant NPM1 [RNA-Seq]
GEO Series GSE227022. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
Coupled single-cell epigenome editing and profiling reveals causal gene regulatory networks [Perturb-ATAC (GBC/sgRNA)]
GEO Series GSE116285. Homo sapiens. 4208 samples. Type: Other.
Characterization of a barley (Hordeum vulgare L.) mutant with Multiple Stem Nodes and Spikes and Dwarf (msnsd) and fine-mapping of its causal gene
GEO Series GSE235622. Hordeum vulgare. 6 samples. Type: Expression profiling by high throughput sequencing.
Learning causal networks using inducible transcription factors and transcriptome-wide time series
GEO Series GSE142864. Saccharomyces cerevisiae. 1768 samples. Type: Expression profiling by array.
Single nuclei RNAseq analysis of HD mouse model and human brain reveals impaired 1 oligodendrocyte maturation and potential causal regulators
GEO Series GSE180928. Homo sapiens. 32 samples. Type: Expression profiling by high throughput sequencing.
Exome sequencing reveals the genetic architecture of non-syndromic orofacial clefts and identifies BOC as a novel causal gene
GEO Series GSE292867. Danio rerio. 6 samples. Type: Expression profiling by high throughput sequencing.
Single-cell multiome of the human retina and deep learning nominate causal variants in complex eye diseases
GEO Series GSE196235. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes
GEO Series GSE116497. Homo sapiens. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Assessing the ability of various genomic features to prioritize causal non-coding variants associated with diseases and traits [ATAC-seq]
GEO Series GSE136686. Homo sapiens. 9 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Genome-wide enhancer-gene regulatory maps link causal variants to target genes underlying human colorectal cancer risk
GEO Series GSE222770. Homo sapiens. 40 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Human and rat skeletal muscle single-nuclei multi-omic integrative analyses nominate causal cell types, regulatory elements, and SNPs for complex traits
GEO Series GSE178735. Rattus norvegicus; Homo sapiens. 19 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; 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.