home > sra-sample > SRS1053688
identifier SRS1053688
type sra-sample
sameAs
biosample　 SAMN03578339
organism Homo sapiens
attributes
gap_accession　 phs000288
submitter handle　 NHGRI_Ciliopathies_Exome
biospecimen repository　 NHGRI_Ciliopathies_Exome
study name　 Ciliopathies Exome Sequencing Initiative
study design　 Case-Control
biospecimen repository sample id　 4257462358
submitted sample id　 4257462358
submitted subject id　 4257462358
gap_sample_id　 1549488
gap_subject_id　 1195327
sex　 female
study disease　 Congenital Abnormalities
body site　 whole blood
histological type　 whole blood
analyte type　 DNA
is tumor　 No
subject is affected　 Yes
molecular data type　 SNP/CNV Genotypes (NGS)
gap_consent_code　 1
gap_consent_short_name　 GRU
properties　▽ 
{...}
dbXrefs
bioproject　 PRJNA74825
sra-run　 SRR2232883
sra-submission　 SRA291502
biosample　 SAMN03578339
sra-study　 SRP003277
sra-experiment　 SRX1179738
distribution JSONJSON-LD
Download
SRA291502.sample.xml　 HTTPS FTP
status public
visibility controlled-access
dateCreated 2015-09-02T22:35:20Z
dateModified 2021-08-28T02:23:27Z
datePublished 2017-11-16T21:47:31Z