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Accession: PRJNA523250 ID: 523250

RNA sequencing of isogenic BRCA2 haploinsufficient vs. wild-type T-ALL cells (human)

See Genome Information for Homo sapiens
We found a high frequency of heterozygous Fanconi-BRCA pathway mutations in pediatric T-ALL. More...
AccessionPRJNA523250; GEO: GSE126780
Data TypeTranscriptome or Gene expression
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsPouliot GP et al., "Fanconi-BRCA pathway mutations in childhood T-cell acute lymphoblastic leukemia.", PLoS One, 2019;14(11):e0221288
SubmissionRegistration date: 19-Feb-2019
Boston Children's Hospital
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments12
Publications
PubMed1
PMC1
Other datasets
BioSample12
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Supplementary Mbytes2
SRA Data Details
ParameterValue
Data volume, Gbases76
Data volume, Mbytes29875

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