Find research datasets worth reusing
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”
Congenital scolisis may be associated with both of rare mutation and allele-specific methylation
GEO Series GSE58104. Homo sapiens. 4 samples. Type: Methylation profiling by high throughput sequencing.
Loss of the Maternal Effect Gene Nlrp2 Impairs Embryonic and Extra-Embryonic Development, Unveiling a Novel Cause of Congenital Anomalies
GEO Series GSE274909. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing.
The osteogenic capacity and lncRNA/mRNA expression profile of periosteal-derived mesenchymal stem cells of congenital pseudarthrosis of the tibia
GEO Series GSE200069. Homo sapiens. 10 samples. Type: Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing.
Comparative transcriptome analyses highlight distinct pathogenetic mechanisms for pleuropulmonary blastoma and congenital pulmonary airway malformations I
GEO Series GSE311205. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
NAA15 haploinsufficiency can cause congenital heart disease and perturbs protein levels in induced pluripotent stem cells
GEO Series GSE160809. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
Comparative transcriptome analyses highlight distinct pathogenetic mechanisms for pleuropulmonary blastoma and congenital pulmonary airway malformations II
GEO Series GSE311209. Homo sapiens. 7 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Non-viral in situ gene editing effectively and safely rescues congenital ichthyosis-causing mutations in human skin
GEO Series GSE314473. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
Loss of Maenli lncRNA expression causes engrailed-1 dependent congenital limb malformations [Capture Hi-C]
GEO Series GSE137333. Mus musculus. 11 samples. Type: Other.
A Congenital Anemia Dissociates the Pleiotropic Functions of Master Transcription Factor GATA1 [Patient scATAC-seq]
GEO Series GSE155255. Homo sapiens. 1 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
A Congenital Anemia Dissociates the Pleiotropic Functions of Master Transcription Factor GATA1 [G1E_RNAseq]
GEO Series GSE133403. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing.
Functional dissection of human cardiac enhancers and non-coding de novo variants in congenital heart disease
GEO Series GSE210376. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing; Other.
Targeting Galectin-3 to modulate inflammation in LAMA2-deficient congenital muscular dystrophy
GEO Series GSE292894. Mus musculus. 18 samples. Type: Expression profiling by high throughput sequencing.
Serial Inversions Induce Tissue-specific Architectural Stripes, Gene Misexpression and Congenital Malformations [Hi-C]
GEO Series GSE116791. Mus musculus. 3 samples. Type: Other.
Early-life thymectomy leads to an increase of granzyme-producing γδ T cells in children with congenital heart disease
GEO Series GSE274083. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Effect of treprostinil on rabbit lungs with congenital diaphragmatic hernia
GEO Series GSE220739. Oryctolagus cuniculus. 8 samples. Type: Expression profiling by high throughput sequencing.
Macrophage depletion blocks congenital SARM1-dependent neuropathy
GEO Series GSE210403. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
Similar metabolic pathways are affected in both Congenital Myasthenic Syndrome-22 and Prader-Willi Syndrome
GEO Series GSE261165. Mus musculus. 16 samples. Type: Expression profiling by high throughput sequencing.
A Congenital Anemia Dissociates the Pleiotropic Functions of Master Transcription Factor GATA1 [Patient scRNA-seq]
GEO Series GSE155254. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing.
Mutations in Bcl9 and Pygo genes cause congenital heart defects by tissue-specific perturbation of Wnt/β-catenin signaling (ChIP-seq data set)
GEO Series GSE110781. Mus musculus. 7 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
FOXK2 in Skeletal Muscle Development: A New Pathogenic Gene for Congenital Myopathy with Ptosis
GEO Series GSE291642. Mus musculus. 16 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy 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.