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1,890
datasets available to search
ShareScore release 0.9.0
Dataset results
1,890 results for “Defects”
Prenatal SMN-dependent defects in translation uncover a reversible primary ciliopathy in spinal muscular atrophy
GEO Series GSE295681. Mus musculus. 12 samples. Type: Other.
Molecular Signatures of cardiac defects in Down syndrome lymphoblastoid cell lines (congenital heart disease)
GEO Series GSE34457. Homo sapiens. 43 samples. Type: Expression profiling by array.
Deletion of HDAC1 induces caspase-independent autophagic cell death and mitotic defect in Hep3B cells
GEO Series GSE31358. Homo sapiens. 2 samples. Type: Expression profiling by array.
Direct and indirect transcriptional effects of abiotic stress in Zea mays plants defective in RNA-directed DNA methylation
GEO Series GSE179629. Zea mays. 12 samples. Type: Expression profiling by high throughput sequencing.
Tracing the molecular route to progression in miRNA biogenesis-defective thyroid lesions [InfiniumMethylationData]
GEO Series GSE300956. Homo sapiens. 12 samples. Type: Methylation profiling by genome tiling array; Third-party reanalysis.
A BRCA1 coiled-coil domain variant disrupting PALB2 interaction predisposes to mammary tumors with a targetable defect in homologous recombination repair [RNA-seq]
GEO Series GSE182448. Mus musculus. 73 samples. Type: Expression profiling by high throughput sequencing.
Duplication of autism-related gene Chd8 leads to behavioral hyperactivity and neurodevelopmental defects in mice
GEO Series GSE263334. Mus musculus. 40 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Modelling and rescuing neurodevelopmental defect of Down syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21
GEO Series GSE52251. Homo sapiens. 9 samples. Type: Expression profiling by high throughput sequencing; Genome variation profiling by array.
Phenotyping spermatogenic defects by single-cell expression profiling
GEO Series GSE113293. Mus musculus. 27 samples. Type: Expression profiling by high throughput sequencing.
Gene expression changes in dauer defective strains
GEO Series GSE89295. Caenorhabditis elegans. 35 samples. Type: Expression profiling by high throughput sequencing.
Myocardial Reprogramming by HMGN1 Underlies Heart Defects in Trisomy 21 [scRNA-seq]
GEO Series GSE306773. Homo sapiens; Mus musculus. 29 samples. Type: Expression profiling by high throughput sequencing.
A human mutation in STAT3 promotes type 1 diabetes through a defect in CD8+ T cell tolerance [scATAC]
GEO Series GSE173412. Mus musculus. 2 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Age-related epithelial defects limit thymic function and regeneration [bulk]
GEO Series GSE240017. Mus musculus. 13 samples. Type: Expression profiling by high throughput sequencing.
Centromeric R loops contribute to defects in kinetochore assembly and chromosomal instability
GEO Series GSE151849. Saccharomyces cerevisiae. 8 samples. Type: Other.
Opposing Roles for C/EBPα and Notch in Irradiation-induced Hematopoietic Stem Cell Defects
GEO Series GSE61602. Mus musculus. 18 samples. Type: Expression profiling by high throughput sequencing.
Defects in the alternative splicing-dependent regulation of REST cause deafness - [mouse cultured organ of Corti].
GEO Series GSE111603. Mus musculus. 16 samples. Type: Expression profiling by high throughput sequencing.
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation.
GEO Series GSE138864. Homo sapiens. 6 samples. Type: Methylation profiling by genome tiling array.
PRPF8-mediated dysregulation of hBrr2 helicase disrupts human spliceosome kinetics and 5'-splice-site selection causing tissue-specific defects
GEO Series GSE236702. Homo sapiens. 96 samples. Type: Expression profiling by high throughput sequencing.
A BRCA1 coiled-coil domain variant disrupting PALB2 interaction predisposes to mammary tumors with a targetable defect in homologous recombination repair [CNV-seq]
GEO Series GSE182449. Mus musculus. 101 samples. Type: Other.
Dyw2-DYW2_OTP100: Identification of the transcriptome defects (nuclear and organelles) of the T-DNA KO mutants of DYW2 and OTP100
GEO Series GSE100298. Arabidopsis thaliana. 12 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.