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2,880
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ShareScore release 0.9.0
Dataset results
2,880 results for “variant”
Copy Number variants in Mallotus villosus
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Data from: A synonymous germline variant in a gene encoding a cell adhesion molecule is associated with cutaneous mast cell tumour development in Labrador and Golden Retrievers
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Data from: Admixture and the organization of genetic diversity in a butterfly species complex revealed through common and rare genetic variants
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VCF of structural variant calls of Nanopore data aligned to dm6 reference genome
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Classification of Type 2 Diabetes Genetic Variants and a Novel Genetic Risk Score Association with Insulin Clearance
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Data from: Social chromosome variants differentially affect queen determination and the survival of workers in the fire ant Solenopsis invicta
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Natural variation for carotenoids in fresh kernels is controlled by uncommon variants in sweet corn
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Data from: Phylotranscriptomic analysis uncovers a wealth of tissue inhibitor of metalloproteinases variants in echinoderms
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The modularity of a social group does not affect the transmission speed of a novel, socially learned behaviour, or the formation of local variants
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mRNA vaccine-induced T cells respond identically to SARS-CoV-2 variants of concern but differ in longevity and homing properties depending on prior infection status
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UNC93B1 variants underlie TLR7-dependent autoimmunity
GEO Series GSE250223. Homo sapiens. 1 samples. Type: Expression profiling by high throughput sequencing.
Elimination of mitochondrial DNA variants by nuclear genome transfer in human oocytes
GEO Series GSE42077. Homo sapiens. 11 samples. Type: Expression profiling by array.
A practical evaluation of alignment algorithms for RNA variant calling analysis
GEO Series GSE110114. Homo sapiens. 13 samples. Type: Expression profiling by high throughput sequencing.
Extensive genetic diversity and substructuring among zebrafish strains revealed through copy number variant analysis (CGH)
GEO Series GSE33962. Danio rerio. 3 samples. Type: Genome variation profiling by genome tiling array.
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.
The histone H3 variant H3.3 regulates gene body DNA methylation [ChIP-seq]
GEO Series GSE96834. Arabidopsis thaliana. 20 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
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.
The histone chaperone ANP32B regulates chromatin incorporation of the atypical human histone variant macroH2A
GEO Series GSE241387. Homo sapiens. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Post-zygotic structural variants in histologically normal breast tissue may predispose to sporadic breast cancer [SET 6]
GEO Series GSE64724. Homo sapiens. 100 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
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.
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.