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Accession: PRJNA284111 ID: 284111

Homo sapiens (human)

Homo sapiens Genome sequencing

See Genome Information for Homo sapiens
Whole-exome sequencing identifies a de novo mutation in TRPM4 causing congenital atrial septal defects
AccessionPRJNA284111
Data TypeGenome sequencing
ScopeMonoisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 15-May-2015
Chinese Academy of Sciences
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments3
Other datasets
BioSample3
SRA Data Details
ParameterValue
Data volume, Gbases24
Data volume, Mbytes11596

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