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1,336
datasets available to search
ShareScore release 0.9.0
Dataset results
1,336 results for “congenital”
PKN2 deficiency leads both to prenatal ‘congenital’ cardiomyopathy and defective angiotensin II stress responses
GEO Series GSE206779. Mus musculus. 20 samples. Type: Expression profiling by high throughput sequencing.
A tracheal aspirate-derived airway basal cell model reveals a proinflammatory epithelial defect in congenital diaphragmatic hernia (ATAC-Seq)
GEO Series GSE211788. Homo sapiens. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Differential contributions of fetal mononuclear phagocytes to Zika neuroinvasion versus neuroprotection during congenital infection
GEO Series GSE267677. Mus musculus. 3 samples. Type: Expression profiling by high throughput sequencing.
Serial Inversions Induce Tissue-specific Architectural Stripes, Gene Misexpression and Congenital Malformations [RNA-Seq]
GEO Series GSE116793. Mus musculus. 23 samples. Type: Expression profiling by high throughput sequencing.
A Congenital Anemia Dissociates the Pleiotropic Functions of Master Transcription Factor GATA1 [G1E_ATACseq]
GEO Series GSE133404. Mus musculus. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Loss of Maenli lncRNA expression causes engrailed-1 dependent congenital limb malformations [scRNA-seq]
GEO Series GSE149368. Mus musculus. 3 samples. Type: Expression profiling by high throughput sequencing.
A Congenital Anemia Dissociates the Pleiotropic Functions of Master Transcription Factor GATA1 [Patient_RNAseq]
GEO Series GSE133414. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Serial Inversions Induce Tissue-specific Architectural Stripes, Gene Misexpression and Congenital Malformations [cHi-C]
GEO Series GSE116792. Mus musculus. 7 samples. Type: Other.
A Switch in Iron Transport Mechanisms Defines Novel Forms of Congenital Chronic Kidney Disease [P60 Tfr1KO;KspCre]
GEO Series GSE100253. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Complex DNA Structural Variant on Chromosome 2 in a Pediatric Patient with Development Delay and Congenital Malformation
GEO Series GSE296122. Homo sapiens. 3 samples. Type: Genome variation profiling by array.
EPIC analysis of Brazilian babies born with congenital microcephaly
GEO Series GSE145233. Homo sapiens. 45 samples. Type: Methylation profiling by genome tiling array.
A Congenital Anemia Dissociates the Pleiotropic Functions of Master Transcription Factor GATA1 [G1E_ChIPseq]
GEO Series GSE133409. Mus musculus. 9 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Neuregulin 1 type III reduces severity in a mouse model of Congenital Hypomyelination Neuropathy
GEO Series GSE101808. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing.
Histological and single cell transcriptomic analysis of human retinal organoid models of Leber Congenital Amaurosis identifies endoplasmic reticulum stress as a common degenerative pathway
GEO Series GSE152212. Homo sapiens. 51 samples. Type: Expression profiling by high throughput sequencing.
A Congenital Anemia Dissociates the Pleiotropic Functions of Master Transcription Factor GATA1 [Beta-estradiol_RNAseq]
GEO Series GSE133415. Mus musculus. 16 samples. Type: Expression profiling by high throughput sequencing.
Human stem cell-derived cardiomyocytes integrate into the heart of monkeys with surgically-created congenital-like cardiac defect
GEO Series GSE234206. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Application of Array CGH technique for the clinical diagnosis of developmental delay and congenital malformations in Saudi Arabia [244k]
GEO Series GSE181995. Homo sapiens. 11 samples. Type: Genome variation profiling by genome tiling array.
In vivo verification of the pathophysiology of lipoid congenital adrenal hyperplasia in the adrenal cortex
GEO Series GSE123300. Mus musculus. 13 samples. Type: Expression profiling by high throughput sequencing.
Application of Array CGH technique for the clinical diagnosis of developmental delay and congenital malformations in Saudi Arabia
GEO Series GSE182101. Homo sapiens. 63 samples. Type: Genome variation profiling by genome tiling array.
A Switch in Iron Transport Mechanisms Defines Novel Forms of Congenital Chronic Kidney Disease [P13 Tfr1KO;Six2Cre]
GEO Series GSE100251. Mus musculus. 6 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.