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Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
1,336
datasets available to search
ShareScore release 0.9.0
Dataset results
1,336 results for “congenital”
Analysis of copy number changes and complex rearrangements in patients with congenital abnormalities
GEO Series GSE37906. Homo sapiens. 13 samples. Type: SNP genotyping by SNP array; Genome variation profiling by SNP array.
Gene therapy of dominant CRX-Leber congenital amaurosis using patient retinal organoids
GEO Series GSE153101. Homo sapiens. 43 samples. Type: Expression profiling by high throughput sequencing.
Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring [case 2]
GEO Series GSE65452. Homo sapiens. 2 samples. Type: Genome variation profiling by SNP array; SNP genotyping by SNP array.
Maternal Cholesterol Deficiency Predisposes Congenital Heart Defect Risk
GEO Series GSE307566. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Differentially expressed tRNA-derived fragments in bovine fetuses with assisted reproduction induced congenital overgrowth syndrome
GEO Series GSE213525. Bos indicus x Bos taurus. 17 samples. Type: Expression profiling by high throughput sequencing.
Integrated multiomic characterization of congenital heart disease [RNA-Seq]
GEO Series GSE203274. Homo sapiens. 43 samples. Type: Expression profiling by high throughput sequencing.
Dynamics and variability of transcriptomic dysregulation in congenital myotonic dystrophy during childhood development
GEO Series GSE201255. Homo sapiens. 86 samples. Type: Expression profiling by high throughput sequencing.
Transcriptomics integrated with metabolomics reveals partial molecular mechanisms of nutritional risk and neurodevelopment in children with congenital heart disease
GEO Series GSE267250. Homo sapiens. 30 samples. Type: Expression profiling by high throughput sequencing.
The miRNA profiles of amniotic fluid-derived extracellular vesicles of congenital diaphragmatic hernia patients.
GEO Series GSE240554. Homo sapiens. 45 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Somatic CNV profile of congenital ectopic thyroids
GEO Series GSE17463. Homo sapiens. 3 samples. Type: Genome variation profiling by genome tiling array.
Gene expression profile of PMM2_CDG (Congenital Disorder of Glycosylation) B lymphoblastoid cell lines (B-LCL)
GEO Series GSE145082. Homo sapiens. 14 samples. Type: Expression profiling by array.
Blood genome expression Profiles in Infants with Congenital Cytomegalovirus Infection: Is the asymptomatic infant truly asymptomatic?
GEO Series GSE108211. Homo sapiens. 158 samples. Type: Expression profiling by array.
The miRNA profiles of amniotic fluid-derived extracellular vesicles and fetal lung tissue of nitrofen-induced congenital diaphragmatic hernia rat model.
GEO Series GSE240558. Rattus norvegicus. 30 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Congenital T cell activation blocks transitional to follicular B cell maturation in humans
GEO Series GSE188449. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Single cell transcriptomic profiling of microvascular endothelial cell heterogeneity in congenital diaphragmatic hernia
GEO Series GSE196313. Rattus norvegicus. 4 samples. Type: Expression profiling by high throughput sequencing.
Defective SEC61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia
GEO Series GSE137496. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing.
Molecular Basis of Renal Adaptation in a Murine Model of Congenital Obstructive Nephropathy
GEO Series GSE48041. Mus musculus. 24 samples. Type: Expression profiling by array.
OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness
GEO Series GSE52006. Mus musculus. 20 samples. Type: Expression profiling by high throughput sequencing.
Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring [case 3]
GEO Series GSE65453. Homo sapiens. 3 samples. Type: Genome variation profiling by genome tiling array.
Genetic disarray follows mutant KLF1-E325K expression in a congenital dyserythropoietic anemia patient
GEO Series GSE128718. Homo sapiens. 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.