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69
datasets available to search
ShareScore release 0.9.0
Dataset results
69 results for “biallelic”
Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with Multiple Myeloma
GEO Series GSE164551. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Integrative genomics analysis of genes with biallelic loss and its relation to the expression of mRNA and micro-RNA in esophageal squamous cell carcinoma
GEO Series GSE66274. Homo sapiens. 60 samples. Type: Other.
SNP confirmation: Sequencing of PCR amplicons that contained potential biallelic SNPs in HD-B and DM1-A patient cells.
GEO Series GSE148181. Homo sapiens. 126 samples. Type: Other.
Biallelic TET2 mutation sensitizes to 5’-azacitidine in acute myeloid leukemia. Stolzel et al. JCI Insight. [RNA-Seq]
GEO Series GSE218227. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Human germline biallelic complete NFAT1 deficiency causes the triad of joint contractures, osteochondromas, and susceptibility to B cell malignancy
GEO Series GSE193415. Homo sapiens. 20 samples. Type: Expression profiling by high throughput sequencing.
Gene Therapy in Subjects With Biallelic RPE65 Mutation-associated Retinal Dystrophy
ClinicalTrials.gov study NCT05858983. IPD Sharing: NO. Countries: 1. Publications: 0.
The Safety and Efficacy of ZVS106e in the Treatment of IRDs Caused by Biallelic Mutations in ABCA4
ClinicalTrials.gov study NCT07241169. IPD Sharing: NO. Countries: 0. Publications: 0.
A Clinical Trial of EHT102 Injection in Pediatric Patients With Biallelic hOTOF Mutations
ClinicalTrials.gov study NCT07288580. IPD Sharing: NO. Countries: 1. Publications: 0.
A Study of CHeckpoint Inhibitors in Men With prOgressive Metastatic Castrate Resistant Prostate Cancer Characterized by a Mismatch Repair Deficiency or Biallelic CDK12 Inactivation
ClinicalTrials.gov study NCT04104893. IPD Sharing: NO. Countries: 1. Publications: 0.
A biallelic multiple nucleotide length polymorphism explains functional causality at the 5p15.33 prostate cancer risk locus
GEO Series GSE231751. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Biallelic mutations in the 3’ exonuclease TOE1 cause Pontocerebellar Hypoplasia Type 7 and result in snRNA processing defects
GEO Series GSE71536. Homo sapiens. 154 samples. Type: Expression profiling by high throughput sequencing.
Transcriptome analysis of patient derived induced pluripotent stem cell derived cardiomyocytes with severe, early onset hypertrophic cardiomyopathy due to biallelic MYBPC3 variants c.442G>A and c.506-
GEO Series GSE274124. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Biallelic non-productive enhancer-promoter interaction precedes imprinted expression of KcnK9 during mouse neural commitment
GEO Series GSE244147. Mus musculus. 41 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other.
Biallelic non-productive enhancer-promoter interaction precedes imprinted expression of KcnK9 during mouse neural commitment [RNA-seq]
GEO Series GSE244146. Mus musculus. 8 samples. Type: Expression profiling by high throughput sequencing.
Effects of Arid1a knockout in murine ovarian endometrioid carcinomas with biallelic inactivation of Apc and Pten
GEO Series GSE67695. Mus musculus. 6 samples. Type: Expression profiling by array.
Biallelic non-productive enhancer-promoter interaction precedes imprinted expression of KcnK9 during mouse neural commitment [ChIP-seq]
GEO Series GSE244144. Mus musculus. 12 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
A biallelic multiple nucleotide length polymorphism explains functional causality at the 5p15.33 prostate cancer risk locus [ChIP-Seq]
GEO Series GSE231748. Homo sapiens. 3 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Biallelic BRF2 mutations cause syndromic immunodeficiency and change RNA polymerase III-mediated transcription
GEO Series GSE280098. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
RNA expression in KATOIII cells harboring biallelic deletions of the +22.6-kb site, epithelial-specific enchancer of ABO gene
GEO Series GSE169059. Homo sapiens. 3 samples. Type: Expression profiling by high throughput sequencing.
Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression (2)
GEO Series GSE35552. Drosophila melanogaster. 18 samples. Type: Expression profiling by 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.