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Accession: PRJNA560894 ID: 560894

Molecular insight into the Lin28R192G mutation in human ESCs and Parkinson's disease

This SuperSeries is composed of the SubSeries listed below. Overall design: Refer to individual Series
AccessionPRJNA560894; GEO: GSE135996
TypeUmbrella project
SubmissionRegistration date: 19-Aug-2019
Genomics Core Facility, Biomedical research institute, Seoul national University Hospital
RelevanceSuperseries
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments5
Other datasets
BioSample5
GEO DataSets3
GEO Data Details
ParameterValue
Data volume, Supplementary Mbytes2
SRA Data Details
ParameterValue
Data volume, Gbases48
Data volume, Mbytes25323
Molecular insight into the Lin28R192G mutation in human ESCs and Parkinson's disease encompasses the following 2 sub-projects:
Project TypeNumber of Projects
Transcriptome or Gene expression2
BioProject
accession
OrganismTitle
PRJNA560904Homo sapiensLin28R192G mutation in Parkinsons's disease (Genomics Core Facility, Biomedical...)
PRJNA560905Homo sapiensMolecular insight into the Lin28R192G mutation in human ESCs (Genomics Core Facility, Biomedical...)

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