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69
datasets available to search
ShareScore release 0.9.0
Dataset results
69 results for “biallelic”
SuperSeries=Mouse neural stem and progenitor cells (NSPC) derived from embryonic stem cells, with biallelic Sox2 enhancer cluster deletions
GEO Series GSE237778. Mus musculus. 20 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Gene expression profiles of mono- and biallelic CEBPA mutations in cytogenetically normal AML
GEO Series GSE15210. Homo sapiens. 61 samples. Type: Expression profiling by array.
Biallelic TET2 mutation sensitizes to 5’-azacitidine in acute myeloid leukemia. Stolzel et al. JCI Insight.
GEO Series GSE218228. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing; Methylation profiling by array.
Biallelic deleterious variants in SNAPIN, a retrograde dynein adaptor, cause a prenatal-onset neurodevelopmental disorder [2]
GEO Series GSE298994. Danio rerio. 6 samples. Type: Expression profiling by high throughput sequencing.
A biallelic multiple nucleotide length polymorphism explains functional causality at the 5p15.33 prostate cancer risk locus [ATAC-Seq]
GEO Series GSE231750. Homo sapiens. 3 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Allele-specific expression in a family quartet with autism reveals mono-to-biallelic switch and novel transcriptional processes
GEO Series GSE98581. Homo sapiens. 4 samples. Type: Expression profiling by high throughput sequencing; Other.
Biallelic non-productive enhancer-promoter interaction precedes imprinted expression of KcnK9 during mouse neural commitment [Cut&Run]
GEO Series GSE244145. Mus musculus. 12 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
A pilot study of integrative genomics analysis of genes with biallelic loss and its relation to the expression of mRNA and micro-RNA in esophageal squamous cell cancer
GEO Series GSE38129. Homo sapiens. 60 samples. Type: Expression profiling by array.
Biallelic TET2 mutation sensitizes to 5’-azacitidine in acute myeloid leukemia. Stolzel et al. JCI Insight. [Illumina Infinium]
GEO Series GSE217940. Homo sapiens. 6 samples. Type: Methylation profiling by array.
Bulk ATAC-seq of mouse neural stem and progenitor cells (NSPC) derived from embryonic stem cells, with biallelic Sox2 enhancer cluster deletions
GEO Series GSE237777. Mus musculus. 6 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression (1)
GEO Series GSE35551. Homo sapiens. 7 samples. Type: Expression profiling by array.
Biallelic non-productive enhancer-promoter interaction precedes imprinted expression of KcnK9 during mouse neural commitment [4C-seq]
GEO Series GSE244143. Mus musculus. 9 samples. Type: Other.
Biallelic variants in SNUPN cause a limb girdle muscular dystrophy with myofibrillar-like features
GEO Series GSE253519. Homo sapiens. 5 samples. Type: Expression profiling by high throughput sequencing.
Biallelic deleterious variants in SNAPIN, a retrograde dynein adaptor, cause a prenatal-onset neurodevelopmental disorder [1]
GEO Series GSE298991. Danio rerio. 4 samples. Type: Expression profiling by high throughput sequencing.
Biallelic RNU12 noncoding variants cause CDAGS syndrome
GEO Series GSE155099. Homo sapiens. 5 samples. Type: Expression profiling by high throughput sequencing.
Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression
GEO Series GSE35554. Drosophila melanogaster; Mus musculus; Homo sapiens. 33 samples. Type: Expression profiling by array; Expression profiling by high throughput sequencing.
Biallelic variants in CSPG4 cause a novel neurodevelopmental disorder with intellectual disability, global developmental delay and facial anomalies
GEO Series GSE229401. Danio rerio. 4 samples. Type: Expression profiling by high throughput sequencing.
A novel biallelic missense variant in the BTB domain of ZBTB24 leads to Immunodeficiency, Centromeric instability and Facial anomalies type 2 syndrome
GEO Series GSE249219. Homo sapiens. 5 samples. Type: Methylation profiling by genome tiling array.
Biallelic null variants in PNPLA8 cause microcephaly through the reduced abundance of basal radial gliaナカセンセイキニュウ
GEO Series GSE229956. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing.
Biallelic null variants in PNPLA8 cause microcephaly through the reduced abundance of basal radial glia
GEO Series GSE248252. Homo sapiens. 2 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.