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1,336
datasets available to search
ShareScore release 0.9.0
Dataset results
1,336 results for “congenital”
Muscle from patients with mitochondrial myopathies and congenital muscular dystrophies versus normal human muscle
GEO Series GSE43698. Homo sapiens. 29 samples. Type: Expression profiling by array.
RNAseq of periosteal stem/progenitor cells from patients with congenital pseudarthrosis of the tibia
GEO Series GSE234071. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing.
The destiny of the resistance/susceptibility against GCRV has been congenitally destined by epigenetic mechanism in CIK cells (MeDIP-seq)
GEO Series GSE87405. Ctenopharyngodon idella. 3 samples. Type: Methylation profiling by high throughput sequencing.
The destiny of the resistance/susceptibility against GCRV has been congenitally destined by epigenetic mechanism in CIK cells [miRNA-seq]
GEO Series GSE87413. Ctenopharyngodon idella. 3 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Molecular Features of Congenital Cytomegalovirus Infection in Neonatal Mouse Brain at Single-cell Resolution
GEO Series GSE282712. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing.
Epigenomic signatures of accelerated epigenetic aging are associated with congenital heart disease in newborns
GEO Series GSE293799. Homo sapiens. 59 samples. Type: Methylation profiling by array.
Endothelial RNF20 Suppresses Endothelial-to-Mesenchymal Transition and Safeguards Physiological Angiocrine Signaling to Prevent Congenital Heart Disease [Heart_scRNAseq_E11_5_Cdh5cre_Rnf20KO]
GEO Series GSE246905. Mus musculus. 2 samples. Type: Expression profiling by high throughput sequencing.
RNA-seq of hiPSCs-derived NPCs from 3 pairs of dizygotic discordant twins for Congenital Zika syndrome
GEO Series GSE102128. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Maternal Vitamin C Deficiency and Genetic Risk Factors Contribute to Congenital Malformations through Dysregulation of DNA Methylation.
GEO Series GSE295926. Mus musculus. 67 samples. Type: Methylation profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
Maternal Vitamin C Deficiency and Genetic Risk Factors Contribute to Congenital Malformations through Dysregulation of DNA Methylation. [WGBS E11.5]
GEO Series GSE295922. Mus musculus. 8 samples. Type: Methylation profiling by high throughput sequencing.
Repression of Ect2 induces cytokinesis failure and decreases heart muscle cell proliferation in congenital heart disease
GEO Series GSE108359. Mus musculus. 33 samples. Type: Expression profiling by high throughput sequencing.
Global interpretation of novel alternative splicing events in human congenital pulmonary airway malformations
GEO Series GSE179404. Homo sapiens. 15 samples. Type: Expression profiling by high throughput sequencing.
Whole-genome methylation study of congenital lung malformations in children
GEO Series GSE174625. Homo sapiens. 29 samples. Type: Methylation profiling by genome tiling array.
Oligogenic inheritance of congenital heart disease involving a NKX2-5 modifier [mouse]
GEO Series GSE111394. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing.
RNA-seq right ventricle congenital heart disease paediatric patients
GEO Series GSE256516. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
Conjunctival mRNA and miRNA expression profiles in congenital aniridia are genotype and phenotype dependent (AKK miRNA)
GEO Series GSE137995. Homo sapiens. 40 samples. Type: Non-coding RNA profiling by array.
The application of second-generation sequencing in congenital pulmonary airway malformations
GEO Series GSE190620. Homo sapiens. 9 samples. Type: Non-coding RNA profiling by high throughput sequencing.
The Tudor-domain protein TDRD7, mutated in congenital cataract, controls the heat shock protein HSPB1 (HSP27) and lens fiber cell morphology
GEO Series GSE134384. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Activation of the interferon type I response rather than autophagy contributes to myogenesis inhibition in congenital DM1 myoblasts
GEO Series GSE97019. Homo sapiens. 12 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Improving Thymus Implantation for Congenital Athymia with Interleukin-7
GEO Series GSE246565. Mus musculus. 8 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.