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428
datasets available to search
ShareScore release 0.9.0
Dataset results
428 results for “Malformations”
PRDM15 loss-of-function causes brain malformations through defective embryonic anterior-posterior patterning
GEO Series GSE125752. Mus musculus. 34 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Combinatorial effects on gene expression at the Lbx1/Fgf8 locus resolve Split-Hand/Foot Malformation type 3 [RNA-seq]
GEO Series GSE223455. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Additional references for: Brain arteriovenous malformations: a review of natural history, pathobiology, and interventions
Open the record for dataset details and reuse information.
Impaired neurovascular remodeling mediated by Apelin signaling and Cdc42 activity in endothelial Rbpj deficient brain arteriovenous malformation [ChIP-seq]
GEO Series GSE223532. Mus musculus. 3 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Epigenetic regulation by Polycomb Repressive Complex 1 promotes Cerebral Cavernous Malformations
GEO Series GSE277234. Danio rerio. 12 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.
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.
Serial Inversions Induce Tissue-specific Architectural Stripes, Gene Misexpression and Congenital Malformations [cHi-C]
GEO Series GSE116792. Mus musculus. 7 samples. Type: Other.
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.
Expression data of miRNAs and mRNAs from the fetal rats with anorectal malformations
GEO Series GSE120445. Rattus norvegicus. 6 samples. Type: Non-coding RNA profiling by array.
Silver nanocolloids affects glycosylation in medaka fish to cause embryonic malformation.
GEO Series GSE106163. Oryzias latipes. 6 samples. Type: Expression profiling by array.
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.
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.
Transcriptome analysis provides insights into the skeletal malformation induced by dietary phospholipids deficiency in largemouth bass (Micropterus salmoides) larvae
GEO Series GSE241086. Micropterus salmoides. 6 samples. Type: Expression 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.
Expression data of miRNAs and lncRNAs from the lumbosacral spinal cord of fetal rats with anorectal malformations in embryonic day 17
GEO Series GSE190331. Rattus norvegicus. 12 samples. Type: Non-coding RNA 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.
Genome-Wide Sequencing Reveals Small Nucleolar RNAs Downregulated in Cerebral Cavernous Malformations
GEO Series GSE111623. Homo sapiens. 6 samples. Type: Non-coding RNA 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.
Somatic variants of MAP3K3 are sufficient to cause cerebral cavernous malformations
GEO Series GSE210673. 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.