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Accession: PRJNA281248 ID: 281248

Homo sapiens (human)

Rare variants affecting the Fanconi Anemia/homologous recombination DNA repair gene network confer increased risk for AML and are associated with abnormal karyotype

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This study was to compare gene expression profiles of human AMLs that either carry or lack potentially deleterious variants in genes of the Fanconi Anemia-Homologous Recombination DNA repair network” . More...
AccessionPRJNA281248; GEO: GSE67936
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
SubmissionRegistration date: 15-Apr-2015
University of South Australia
RelevanceMedical
Project Data:
Resource NameNumber
of Links
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots2017210
Data volume, Processed Mbytes56
Data volume, Supplementary Mbytes29

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