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244
datasets available to search
ShareScore release 0.9.0
Dataset results
244 results for “genomic variants”
Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss
GEO Series GSE64088. Homo sapiens. 308 samples. Type: Genome variation profiling by genome tiling array.
Integrative functional genomic analyses identify genetic variants influencing skin pigmentation in Africans
GEO Series GSE240717. Homo sapiens. 42 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Genome-wide analysis of histone H3.1 and H3.3 variants in Arabidopsis thaliana
GEO Series GSE34840. Arabidopsis thaliana. 5 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
Integrated genomics of Crohn’s disease risk variant identifies a role for CLEC12A in antibacterial autophagy
GEO Series GSE69132. Mus musculus. 42 samples. Type: Expression profiling by high throughput sequencing.
A genome-wide approach to identify genetic variants that contribute to etoposide-induced cytotoxicity
GEO Series GSE7792. Homo sapiens. 176 samples. Type: Expression profiling by array.
Integrative functional genomic analyses identify novel genetic variants influencing skin pigmentation in indigenous Africans [Cut&Run, ATAC-seq]
GEO Series GSE240716. Homo sapiens. 7 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Analysis of the Saccharomyces cerevisiae Pan-Genome Reveals a Pool of Copy Number Variants Distributed in Diverse Yeast Strains From Differing Industrial Environments.
GEO Series GSE26689. Saccharomyces bayanus; Saccharomyces cerevisiae. 98 samples. Type: Genome variation profiling by array.
Genome-wide discovery of multiple sclerosis genetic risk variant allelic regulatory activity
GEO Series GSE293036. Homo sapiens. 19 samples. Type: Expression profiling by high throughput sequencing; Other.
Integrative functional genomic analyses identify novel genetic variants influencing skin pigmentation in indigenous Africans [RNA-seq]
GEO Series GSE213142. Homo sapiens. 27 samples. Type: Expression profiling by high throughput sequencing.
Genome-wide maps of histone variant H3.3 occupancy in zebrafish cardiomyocytes
GEO Series GSE81893. Danio rerio. 16 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
A functional genomics atlas enhanced by convolutional neural networks facilitates clinical interpretation of disease relevant variants in non-coding regulatory elements [ATAC-seq]
GEO Series GSE263338. Homo sapiens. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Multiplex generation and single cell analysis of structural variants in mammalian genomes
GEO Series GSE282636. Homo sapiens; Mus musculus. 197 samples. Type: Other; Expression profiling by high throughput sequencing.
Histone Variant H2A.X Plays Novel Roles in Cell Lineage Commitment and Genomic Stability in ESC and iPSC
GEO Series GSE49147. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
A functional genomics atlas enhanced by convolutional neural networks facilitates clinical interpretation of disease relevant variants in non-coding regulatory elements [ChIP-seq]
GEO Series GSE263337. Homo sapiens. 16 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Adaptive Structural Variants Contributing to Human Brain Development Revealed by 1,026 Rhesus Macaque Genomes
GEO Series GSE221928. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Multiplex generation and single cell analysis of structural variants in mammalian genomes [IVT-seq]
GEO Series GSE282633. Homo sapiens; Mus musculus. 20 samples. Type: Other.
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.
Genome-wide analysis of the histone variant H3mm7
GEO Series GSE104389. Mus musculus. 117 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Transcriptional activity of an MPRA library containing sequences of genomic origin bound by the transcription factor CRX measured in retinas from mice carrying pathogenic CRX variants
GEO Series GSE230090. Mus musculus; synthetic construct. 38 samples. Type: Other.
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.
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.