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Accession: PRJNA635176 ID: 635176

Primary ciliary dyskinesia without obvious electron microscopy defects (human)

See Genome Information for Homo sapiens
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This project is a component of the Primary ciliary dyskinesia without obvious electron microscopy defects
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66644 additional projects are related by organism.
This study of 59 primary ciliary dyskinesia (PCD) patients utilized whole-exome capture sequencing to help identify variants that may be causative for PCD. More...
AccessionPRJNA635176; dbGaP: phs002035
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: 26-May-2020
WASHINGTON UNIVERSITY
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments59
Other datasets
BioSample59
Genotype and Phenotype (dbGaP)1
SRA Data Details
ParameterValue
Data volume, Gbases443
Data volume, Tbytes0.18

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