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Accession: PRJNA157243 ID: 157243

Homo sapiens (human)

Swedish Schizophrenia Population-Based Case-control Exome Sequencing

See Genome Information for Homo sapiens
Current findings of the genetic risk of schizophrenia and bipolar disorder emerging from genome wide association studies (GWAS) support a highly polygenic model displaying the full spectrum of causal alleles that includes the extremes of rare, penetrant alleles as well as common alleles of small effect. More...
AccessionPRJNA157243; dbGaP: phs000473
Data TypePhenotype or Genotype
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 1-Jul-2012
MASSACHUSETTS GENERAL HOSPITAL
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments12380
Other datasets
BioSample12380
Genotype and Phenotype (dbGaP)1
SRA Data Details
ParameterValue
Data volume, Gbases94,929
Data volume, Tbytes46.41

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