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Accession: PRJNA163327 ID: 163327

Homo sapiens (human)

Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

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Expression profiling of lymphoblast cell lines of autisms from Simons Simplex Families. More...
AccessionPRJNA163327; GEO: GSE37772
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
PublicationsLuo R et al., "Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.", Am J Hum Genet, 2012 Jul 13;91(1):38-55
SubmissionRegistration date: 4-May-2012
Daniel Geschwind Lab, Human Genetics, UCLA
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots10766914
Data volume, Processed Mbytes256
Data volume, Supplementary Mbytes77

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