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.
1,890
datasets available to search
ShareScore release 0.9.0
Dataset results
1,890 results for “Defects”
Splicing Correction as a Therapeutic Approach for Acetylation-Defective p53 K120R mutation
GEO Series GSE274604. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Defects in placental syncytiotrophoblast cells are a common cause of developmental heart disease
GEO Series GSE204859. Mus musculus. 75 samples. Type: Expression profiling by high throughput sequencing.
Deletion of Gas2l3 in mice leads to specific defects in cardiomyocyte cytokinesis during development
GEO Series GSE91078. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Defects in dosage compensation impact global gene regulation in the mouse trophoblast
GEO Series GSE93031. Mus musculus. 16 samples. Type: Expression profiling by high throughput sequencing.
Maternal CXCR4 deletion results in placental defects and pregnancy loss mediated by immune dysregulation
GEO Series GSE241958. Mus musculus. 1 samples. Type: Expression profiling by high throughput sequencing.
Granulosa cell mevalonate pathway abnormalities contribute to oocyte meiotic defects and aneuploidy
GEO Series GSE175836. Mus musculus; Homo sapiens. 97 samples. Type: Expression profiling by high throughput sequencing; Other.
Granulosa cell mevalonate pathway abnormalities contribute to oocyte meiotic defects and aneuploidy [RNA-seq mouse GC]
GEO Series GSE175834. Mus musculus. 28 samples. Type: Expression profiling by high throughput sequencing.
Impairment of RNA polymerase I elongation rate induces defects in ribosomal RNA processing and ribosome biogenesis
GEO Series GSE196146. Saccharomyces cerevisiae. 6 samples. Type: Other.
Molecular Signatures of cardiac defects in Down syndrome lymphoblastoid cell lines (trisomy 21)
GEO Series GSE34458. Homo sapiens. 23 samples. Type: Expression profiling by array.
Mouse models of neutropenia reveal progenitor-stage-specific defects [CITE-Seq]
GEO Series GSE142341. Mus musculus. 14 samples. Type: Expression profiling by high throughput sequencing.
Search for mitochondrial editing defect in an Arabidopsis PPR mutant
GEO Series GSE144560. Arabidopsis thaliana. 12 samples. Type: Expression profiling by high throughput sequencing.
DNMT3A haploinsufficiency causes dichotomous DNA methylation defects at enhancers in mature human immune cells [RNA-seq]
GEO Series GSE168810. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
Defective autophagy in CD4 T cells drives liver fibrosis via type 3 inflammation
GEO Series GSE292735. Mus musculus. 11 samples. Type: Expression profiling by high throughput sequencing.
Cerebrospinal fluid-driven ependymal motile cilia defects are implicated in multiple sclerosis pathophysiology
GEO Series GSE301791. Rattus norvegicus. 7 samples. Type: Expression profiling by high throughput sequencing.
Loss of G6b-B results in defective TPO signaling and blocks megakaryocyte-lineage differentiation
GEO Series GSE155735. Mus musculus. 16 samples. Type: Expression profiling by high throughput sequencing.
Copy number variations may contribute to congenital heart defect risk greatly by disrupting long noncoding RNAs
GEO Series GSE201076. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
Defective endomembrane dynamics in Rab27a deficiency impairs nucleic acid sensing and cytokine secretion in immune cells
GEO Series GSE272416. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
Functional analysis across model systems implicates ribosomal proteins in growth and proliferation defects associated with hypoplastic left heart syndrome
GEO Series GSE207658. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
Prkar1a haploinsufficiency leads to an overall increase in tumors caused by other genetic defects or chemical induction
GEO Series GSE19576. Mus musculus. 23 samples. Type: Expression profiling by array.
Incomplete repair causes permanent defects in renal medullary structure and function after reversal of urinary obstruction
GEO Series GSE283241. Mus musculus. 3 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.