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.
244
datasets available to search
ShareScore release 0.9.0
Dataset results
244 results for “genomic variants”
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.
Multiplex generation and single cell analysis of structural variants in mammalian genomes [scRNA-seq]
GEO Series GSE282634. Homo sapiens; Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing; Other.
Genomic instability in the naturally and prematurely aged myocardium [variants: data set 1]
GEO Series GSE124083. Mus musculus. 2 samples. Type: Genome variation profiling by high throughput sequencing.
Chromosomal microarray data for validation of copy-number variants detection from a low-coverage whole-genome sequencing approach in clinical samples
GEO Series GSE73191. Homo sapiens. 72 samples. Type: Genome variation profiling by array; Genome variation profiling by SNP array; SNP genotyping by SNP array.
Genomic profiling of active vitamin D colonic responses in African- and European-Americans identifies an ancestry-related regulatory variant of POLB
GEO Series GSE295961. Homo sapiens. 157 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
Elimination of mitochondrial DNA variants by nuclear genome transfer in human oocytes.
GEO Series GSE42271. Homo sapiens. 15 samples. Type: Genome variation profiling by SNP array.
Identification and functional impact of genomic copy number variants in zebrafish, an important human disease model (Zebrafish Strain CNVs) (CGH ZV81M 2)
GEO Series GSE28278. Danio rerio. 76 samples. Type: Genome variation profiling by genome tiling array.
Genome-wide localisation of histone variants in Toxoplasma gondii implicates variant exchange in transcriptional control by demarcation of functional chromatin regions
GEO Series GSE87834. Toxoplasma gondii ME49; Toxoplasma gondii RH. 10 samples. Type: Genome binding/occupancy profiling by genome tiling array.
Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants
GEO Series GSE53351. Homo sapiens. 301 samples. Type: Expression profiling by array.
Genomic instability in the naturally and prematurely aged myocardium [variants: data set 2]
GEO Series GSE129278. Mus musculus. 6 samples. Type: Other.
Subcellular genomics shows pervasive within-mitochondrion single nucleotide variant heteroplasmy as revealed by single mitochondrion sequencing
GEO Series GSE107115. Mus musculus. 158 samples. Type: Expression profiling by high throughput sequencing.
Genome-wide maps of histone variant H3.3 occupancy in zebrafish cardiomyocytes [H3K27Ac]
GEO Series GSE81863. Danio rerio. 2 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Genome-wide maps of enhancer regulation connect risk variants to disease genes
GEO Series GSE285157. Homo sapiens. 16 samples. Type: Expression profiling by high throughput sequencing.
Genome-wide search for exonic variants affecting translational efficiency
GEO Series GSE46195. Homo sapiens. 126 samples. Type: Expression profiling by array.
Multiplex generation and single cell analysis of structural variants in mammalian genomes [Amplicon-seq]
GEO Series GSE282632. Mus musculus; Homo sapiens. 169 samples. Type: Other.
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.
Genome-wide incorporation dynamics reveal distinct categories of turnover for the histone variant H3.3
GEO Series GSE51505. Mus musculus. 45 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
A maternal-effect Padi6 variant causes nuclear and cytoplasmic abnormalities in oocytes as well as failure of epigenetic reprogramming and zygotic genome activation in embryos [WGS]
GEO Series GSE245425. Mus musculus. 1 samples. Type: Other.
Effect of Gfi1 36N variant on genome-wide H3K9 Acetylation patterns
GEO Series GSE71254. Mus musculus; Homo sapiens. 24 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Transcriptomic characterization of CRISPR/Cas9-edited THP1 cells to test the effect of disrupting the 3q23 genomic region containing TB-risk associated variants marking a putative monocyte-specific e
GEO Series GSE134419. Homo sapiens. 46 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.