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376
datasets available to search
ShareScore release 0.9.0
Dataset results
376 results for “Causality”
Data from: Modeling the perception of audiovisual distance: Bayesian causal inference and other models
Open the record for dataset details and reuse information.
Assessing the ability of various genomic features to prioritize causal non-coding variants associated with diseases and traits
GEO Series GSE136703. Homo sapiens; unidentified plasmid. 210 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Other.
Integration of eQTL and single-cell transcriptomics in the human eye identifies causal genes for age-related macular degeneration
GEO Series GSE135092. Homo sapiens. 537 samples. Type: Expression profiling by high throughput sequencing.
Kidney compartment specific eQTL studies highlight causal genes and pathways for renal disease development
GEO Series GSE115098. Homo sapiens. 20 samples. Type: Expression profiling by high throughput sequencing.
Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3’ UTR of FAIM2 (snATAC-Seq)
GEO Series GSE241593. Homo sapiens. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
HALO: Hierarchical Causal Modeling for Single Cell Multi-Omics Data
GEO Series GSE302151. Homo sapiens. 31 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Causal signals between codon bias, mRNA structure and the efficiency of translation and elongation
GEO Series GSE63789. Saccharomyces cerevisiae. 10 samples. Type: Expression profiling by high throughput sequencing; Other.
Human and rat skeletal muscle single-nuclei multi-omic integrative analyses nominate causal cell types, regulatory elements, and SNPs for complex traits [snATAC-seq]
GEO Series GSE178733. Rattus norvegicus; Homo sapiens. 12 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 [MPRA]
GEO Series GSE136702. Homo sapiens; unidentified plasmid. 33 samples. Type: Other.
Human iPSC-derived retinal pigment epithelium: a model system for identifying and functionally characterizing causal variants at AMD risk loci
GEO Series GSE126847. Homo sapiens. 24 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Coupled single-cell epigenome editing and profiling reveals causal gene regulatory networks [scATAC-seq]
GEO Series GSE116248. Homo sapiens. 288 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Coupled single-cell epigenome editing and profiling reveals causal gene regulatory networks [Perturb-ATAC (ATAC)]
GEO Series GSE116249. Homo sapiens. 4207 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
NBL1 Correlates with Renal Phenotypes in Mouse Models of Kidney Disease, but is not Causal: Male Nbl1 HET or WT Mice Treated with Cisplatin or PBS
GEO Series GSE310628. Mus musculus. 31 samples. Type: Expression profiling by high throughput sequencing.
A Dinucleotide-barcode reporter system and application in dissecting the causal rule of regulatory risk SNPs
GEO Series GSE165765. synthetic construct; Homo sapiens. 11 samples. Type: Genome variation profiling by high throughput sequencing.
Exploring the Genetic Basis of Human Population Differences in DNA Methylation and their Causal Impact on Immune Gene Regulation
GEO Series GSE120610. Homo sapiens. 156 samples. Type: Methylation profiling by array.
A biallelic multiple nucleotide length polymorphism explains functional causality at 5p15.33 prostate cancer risk locus [RNA-Seq]
GEO Series GSE231747. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Colocalization of GWAS and molecular QTL signals in human vascular smooth muscle cells predict candidate causal genes for coronary artery disease and vascular disorders
GEO Series GSE193817. Homo sapiens. 284 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.
Dissecting Non-Coding GWAS Loci with High-Resolution 3D Chromatin Interactions Reveals Causal Genes with Relevance to Heart Failure [RNA-seq]
GEO Series GSE281465. Homo sapiens. 3 samples. Type: Expression profiling by high throughput sequencing.
Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3’ UTR of FAIM2 (RNA-Seq)
GEO Series GSE241050. Homo sapiens. 32 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.