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97
datasets available to search
ShareScore release 0.9.0
Dataset results
97 results for “DNA variants”
DNA Repair Function Scores for 2172 Variants in the BRCA1 Amino-Terminus
GEO Series GSE234482. Homo sapiens. 16 samples. Type: Other.
Missense variants in human forkhead transcription factors reveal determinants of forkhead DNA bispecificity
GEO Series GSE297784. Homo sapiens; synthetic construct. 260 samples. Type: Genome binding/occupancy profiling by array.
A multiplexed homology-directed DNA repair assay reveals the impact of over 1,000 BRCA1 missense substitution variants on protein function
GEO Series GSE116427. Homo sapiens. 32 samples. Type: Other.
RING1 missense variants reveal sensitivity of DNA damage repair to H2A monoubiquitination dosage during neurogenesis [scRNA-seq]
GEO Series GSE252449. Homo sapiens. 7 samples. Type: Expression profiling by high throughput sequencing.
Direct recruitment of TONSOKU by the N-terminal tails of histone variants H2A.X and H2A.W coordinates DNA repair
GEO Series GSE293950. Arabidopsis thaliana. 30 samples. Type: Expression profiling by high throughput sequencing.
Functional phenotyping of genomic variants using joint multiomic single-cell DNA-RNA sequencing
GEO Series GSE268646. Homo sapiens; Mus musculus. 17 samples. Type: Expression profiling by high throughput sequencing; Other.
Compendium of Disease-Linked Regulatory DNA Variants and Homeostatic Transcription Factors in Epidermis [mpra_tf_kos]
GEO Series GSE302354. Homo sapiens. 29 samples. Type: Other.
Analysis of the DNA topology upon multiple histone H1 variants depletion by Hi-C experiments
GEO Series GSE172618. Homo sapiens. 6 samples. Type: Other.
Compendium of Disease-Linked Regulatory DNA Variants and Homeostatic Transcription Factors in Epidermis [cutandrun]
GEO Series GSE255543. Homo sapiens. 310 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
NOMe-HiC: joint profiling of genetic variants, DNA methylation, chromatin accessibility, and 3D genome in the same DNA molecule
GEO Series GSE189158. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing; Other.
Whole Exome Sequencing in Finding Causative Variants in Germline DNA Samples From Patients With Hypertension Receiving Bevacizumab for Breast Cancer
ClinicalTrials.gov study NCT02610413. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Whole Exome Sequencing in Finding Causative Variants in Germline DNA Samples From Patients With Peripheral Neuropathy Receiving Paclitaxel for Breast Cancer
ClinicalTrials.gov study NCT02610439. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Evaluation of the Technical Feasibility of Testing ct DNA for Homologous Recombination Gene Variants in Metastatic Prostate Cancer.
ClinicalTrials.gov study NCT05415787. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Whole Exome Sequencing in Finding Causative Variants in Germline DNA Samples From Patients With Congestive Heart Failure Receiving Therapy for Breast Cancer
ClinicalTrials.gov study NCT02610426. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Identification of introduced and stably inherited DNA methylation variants in soybean associated with soybean cyst nematode parasitism
GEO Series GSE130139. Glycine max. 30 samples. Type: Methylation profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
The histone H3 variant H3.3 regulates gene body DNA methylation
GEO Series GSE96873. Arabidopsis thaliana. 25 samples. Type: Methylation profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
Identification of introduced and stably inherited DNA methylation variants in soybean associated with soybean cyst nematode parasitism [RNA-seq]
GEO Series GSE130138. Glycine max. 12 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 [plasmid DNA-seq]
GEO Series GSE263336. Homo sapiens. 4 samples. Type: Other.
MGA-seq is an efficient tool for genetic variants and extrachromosomal DNA detection in cancer cell [RNA-Seq]
GEO Series GSE205281. Homo sapiens. 3 samples. Type: Expression profiling by high throughput sequencing.
Identification of introduced and stably inherited DNA methylation variants in soybean associated with soybean cyst nematode parasitism [MethylC-Seq]
GEO Series GSE130134. Glycine max. 18 samples. Type: Methylation 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.