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Accession: PRJNA280730 ID: 280730

Homo sapiens (human)

A genome-wide analysis of MDS and MDS/MPN patients

See Genome Information for Homo sapiens
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66643 additional projects are related by organism.
To characterize the molecular changes in myelodysplastic syndromes (MDS) and to explore novel genetic abnormalities occurring in these disorders through a genome-wide study in a series of MDS and MDS/MPN patients. More...
AccessionPRJNA280730; GEO: GSE67682
Data TypeVariation
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsAbáigar M et al., "Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes.", PLoS One, 2016;11(10):e0164370
SubmissionRegistration date: 8-Apr-2015
Centro de Investigación del Cáncer
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots40616037
Data volume, Processed Mbytes908
Data volume, Supplementary Mbytes3160

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