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97
datasets available to search
ShareScore release 0.9.0
Dataset results
97 results for “DNA variants”
MGA-seq is an efficient tool for genetic variants and extrachromosomal DNA detection in cancer cell
GEO Series GSE205293. Homo sapiens. 17 samples. Type: Expression profiling by high throughput sequencing; Other.
MGA-seq is an efficient tool for genetic variants and extrachromosomal DNA detection in cancer cell [MGA-Seq]
GEO Series GSE205286. Homo sapiens. 11 samples. Type: Other.
The histone H3 variant H3.3 regulates gene body DNA methylation [BiSulfite-seq]
GEO Series GSE95175. Arabidopsis thaliana. 3 samples. Type: Methylation profiling by high throughput sequencing.
Variants of DNMT3A cause transcript-specific DNA methylation changes
GEO Series GSE103006. Homo sapiens. 24 samples. Type: Methylation profiling by array.
ZBTB10 binds the telomeric variant repeat TTGGGG and interacts with TRF2 [DNA-Seq validation of KO]
GEO Series GSE117213. Homo sapiens. 10 samples. Type: Other.
TONSOKU reads the histone H3.1 variant to mediate DNA repair during replication
GEO Series GSE184738. Arabidopsis thaliana. 20 samples. Type: Expression profiling by high throughput sequencing; Other.
DNA binding analysis of rare variants in homeodomains reveals homeodomain specificity-determining residues
GEO Series GSE233827. Homo sapiens; synthetic construct. 122 samples. Type: Genome binding/occupancy profiling by array.
Chromatin remodeling of histone H3 variants by DDM1 underlies epigenetic inheritance of DNA methylation [bisulfite-seq]
GEO Series GSE231564. Arabidopsis thaliana. 16 samples. Type: Methylation profiling by high throughput sequencing.
Variants of DNMT3A cause transcript-specific DNA methylation and gene expression changes
GEO Series GSE103008. Homo sapiens. 48 samples. Type: Expression profiling by array; Methylation profiling by array.
Chromatin remodeling of histone H3 variants by DDM1 underlies epigenetic inheritance of DNA methylation.
GEO Series GSE231565. Arabidopsis thaliana. 52 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Methylation profiling by high throughput sequencing.
Androgen receptor variants mediate DNA repair after prostate cancer irradiation
GEO Series GSE102164. Homo sapiens. 6 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Histone variant H2AFV equips glioblastoma stem cells with transcriptional potency and efficient DNA damage response [ATAC-seq]
GEO Series GSE152858. Homo sapiens. 6 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Detection of 5mC and 5hmC in DNA templates generated by PCR using modified dCTPs by linear PCR using KTq DNA polymerase variant RIV A8
GEO Series GSE270850. synthetic construct. 3 samples. Type: Other.
Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach
GEO Series GSE94994. Homo sapiens. 159 samples. Type: Genome variation profiling by array.
Chromatin remodeling of histone H3 variants by DDM1 underlies epigenetic inheritance of DNA methylation [ChIP-seq]
GEO Series GSE231563. Arabidopsis thaliana. 36 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
SCN1A pathogenic variants do not have a distinctive blood-derived DNA methylation signature
GEO Series GSE280241. Homo sapiens. 45 samples. Type: Methylation profiling by array.
Detection of 5mC in DNA templates generated by PCR and HeLa human genomic DNA by linear PCR using KTq DNA polymerase variants
GEO Series GSE233599. synthetic construct; Homo sapiens. 18 samples. Type: Other.
RING1 missense variants reveal sensitivity of DNA damage repair to H2A monoubiquitination dosage during neurogenesis [bulk RNA-seq]
GEO Series GSE252447. Homo sapiens. 15 samples. Type: Expression profiling by high throughput sequencing.
Analysis of the DNA accessibility upon multiple histone H1 variants by ATAC-seq (6 samples)
GEO Series GSE100762. Homo sapiens. 6 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Functional DNA methylation signatures for genomic loci that confer an increased risk for autism spectrum disorder: 16p11.2 deletions and CHD8 variants
GEO Series GSE113967. Homo sapiens. 134 samples. Type: Methylation 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.