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1,890
datasets available to search
ShareScore release 0.9.0
Dataset results
1,890 results for “Defects”
DHX9 suppresses spurious RNA processing defects originating from the Alu invasion of the human genome [uvCLAP CLIP-seq]
GEO Series GSE85155. Homo sapiens; Drosophila melanogaster; Mus musculus. 52 samples. Type: Expression profiling by high throughput sequencing; Other.
CAG repeat expansion in the Huntington’s Disease gene correlates with defective linear and back-splicing [smallRNA-seq]
GEO Series GSE175657. Mus musculus. 24 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Maternal obesity induces the meiotic defects and epigenetic alterations during fetal oocyte development [RNA-seq]
GEO Series GSE263548. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Defective RNA processing and ELOA-mediated transcriptional elongation in reversible cellular senescence suggest aging by transcription
GEO Series GSE269948. Homo sapiens. 162 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Other.
Cellular responses in the airway ciliary microenvironment from mouse models of primary ciliary dyskinesia with central pair apparatus defects
GEO Series GSE254100. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Inhibition of BET proteins rescues neural defects in Rett syndrome [HiC-seq]
GEO Series GSE117509. Homo sapiens. 4 samples. Type: Other.
Array profiling of dystrophin-deficient mice with a secondary glycosylation defect
GEO Series GSE16438. Mus musculus. 24 samples. Type: Expression profiling by array.
Ubiquitination of the spliceosome auxiliary factor hnRNPA1 by TRAF6 links chronic innate immune signaling with hematopoietic defects and myelodysplasia
GEO Series GSE64542. Mus musculus. 7 samples. Type: Expression profiling by array.
Distinct pathways for removal of defective RNA polymerase II transcription complexes at a promoter-proximal pause checkpoint [RN21114 Ttchemn-Seq]
GEO Series GSE253353. Homo sapiens. 12 samples. Type: Other.
Biphasic Cell Cycle Defect Causes Impaired Neurogenesis in Down Syndrome [Pluripotency, RNA-Seq]
GEO Series GSE95551. Mus musculus. 15 samples. Type: Expression profiling by high throughput sequencing.
DICER1 hotspot mutations cause defective miRNA processing
GEO Series GSE40965. Mus musculus. 28 samples. Type: Expression profiling by array.
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects
GEO Series GSE242698. Mus musculus. 29 samples. Type: Expression profiling by high throughput sequencing.
ATAC-seq of E9.5 Neural Tube defects mouse brain and E9.5 normal mouse brains
GEO Series GSE299189. Mus musculus. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Identification of transcription termination defects at DNA hypomethylated transcription termination sites in DNA methyltransferase 3a-deficient vertebrates [RNA-Seq]
GEO Series GSE178688. Danio rerio. 2 samples. Type: Expression profiling by high throughput sequencing.
Maternal obesity disrupts histone modifications mediated by Ezh2 and Ampk interactions and induces cell fate defects during embryonic cortical neurogenesis. [ChIP-Seq]
GEO Series GSE255917. Rattus norvegicus. 30 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Downregulation of Endothelin Receptor B Contributes to Defective B Cell Lymphopoiesis in Trisomy 21 Pluripotent Cells
GEO Series GSE110064. Homo sapiens. 6 samples. Type: Expression profiling by array.
Chronic Oxidative DNA Damage Due to DNA Repair Defects Causes Chromosomal Instability in Saccharomyces cerevisiae
GEO Series GSE10152. Saccharomyces cerevisiae. 9 samples. Type: Genome variation profiling by genome tiling array.
RUNX1 Deficiency Cooperates with SRSF2 Mutation to Induce Multi-lineage Hematopoietic Defects Characteristic of Myelodysplastic Syndromes
GEO Series GSE200446. Homo sapiens; Mus musculus. 24 samples. Type: Expression profiling by high throughput sequencing.
Next Generation RNA Sequencing reveals defects in nuclear mRNA maturation of Arabidopsis thaliana lefko1 mutant
GEO Series GSE106459. Arabidopsis thaliana. 2 samples. Type: Other.
QTL-region-specific microrrays reveal differential expression of signaling pathways associated with the liability for the inverted teat defect
GEO Series GSE34240. Sus scrofa. 30 samples. Type: Expression profiling by genome tiling array.
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.