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91
datasets available to search
ShareScore release 0.9.0
Dataset results
91 results for “variant identification”
Identification and Characterization of Genetic Variants in Hereditary Angioedema
ClinicalTrials.gov study NCT05833620. IPD Sharing: NO. Countries: 1. Publications: 0.
Identification and Characterization of Novel Non-Coding Variants That Contribute to Genetic Disorders
ClinicalTrials.gov study NCT04399694. IPD Sharing: YES. Countries: 1. Publications: 0.
Diagnosis of RSTS: Identification of the Acetylation Profiles as Epigenetic Markers for Assessing Causality of CREBBP and EP300 Variants.
ClinicalTrials.gov study NCT04122742. IPD Sharing: NO. Countries: 1. Publications: 0.
Identification and Characterization of Bone-related Genetic Variants in Families
ClinicalTrials.gov study NCT02762318. IPD Sharing: YES. Countries: 1. Publications: 0.
Identification of Viral Variants Involved in the Transmission of Hepatitis C and Characterization of Antigenic and Functional Properties of Their Envelope Glycoproteins
ClinicalTrials.gov study NCT02574884. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Transcriptomic Approach for the Identification and Prioritization of Genome Variants in Neurodevelopmental Disorders With Malformation
ClinicalTrials.gov study NCT06762678. IPD Sharing: UNDECIDED. Countries: 0. 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.
Systematic identification of genotype-dependent enhancer variants in eosinophilic esophagitis and atopic dermatitis [RNA-Seq]
GEO Series GSE232336. Homo sapiens. 10 samples. Type: Expression profiling by high throughput sequencing.
Comprehensive identification of coronary artery disease-associated variants regulating vascular smooth muscle cell gene expression [lentiMPRA]
GEO Series GSE279300. Homo sapiens. 24 samples. Type: Other.
Identification of variant distribution in ethanol-selected sRNA libraries
GEO Series GSE125161. Vibrio cholerae C6706. 7 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Data from: Multiple maize reference genomes impact the identification of variants by GWAS in a diverse inbred panel
Open the record for dataset details and reuse information.
Identification of genes regulated by the MADS transcription factor (TF), SEPALLATA3 spliced variant, SEP3.3 , in the context of the triple sep1 sep2 sep3 mutant background, by RNA-Seq analysis
GEO Series GSE226520. Arabidopsis thaliana. 3 samples. Type: Expression profiling by high throughput sequencing.
Identification and characterization of androgen receptor splice variants preferred bindings that drive prostate cancer progression
GEO Series GSE80743. Homo sapiens. 29 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy 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.
Identification of a Therapeutically Targetable JAK-STAT Enriched Androgen Receptor (AR) and AR Splice Variant Positive Triple Negative Breast Cancer Subtype [MDA-MB-453]
GEO Series GSE245554. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
New strategies for the identification of intronic variants related to splicing events in pancreas cancer [iCELL8]
GEO Series GSE229006. Homo sapiens. 10 samples. Type: Expression profiling by high throughput sequencing.
Identification of Genetic Variants Contributing to Cisplatin-Induced Cytotoxicity using a Genome-wide Approach
GEO Series GSE7761. Homo sapiens. 176 samples. Type: Expression profiling by array.
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.
Identification of genetic variants affecting vitamin D receptor binding and associations with autoimmune disease
GEO Series GSE73254. Homo sapiens. 30 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Systematic Identification of Regulatory Variants Associated with Cancer Risk
GEO Series GSE94140. Homo sapiens; synthetic construct. 4 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.