home > sra-sample > SRS1049612
identifier SRS1049612
type sra-sample
sameAs
biosample　 SAMN03578856
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　 3202990466
submitted sample id　 3202990466
submitted subject id　 3202990466
gap_sample_id　 1549329
gap_subject_id　 1195168
sex　 male
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　 SRR2218357
sra-submission　 SRA291502
biosample　 SAMN03578856
sra-study　 SRP003277
sra-experiment　 SRX1174340
distribution JSONJSON-LD
Download
SRA291502.sample.xml　 HTTPS FTP
status public
visibility controlled-access
dateCreated 2015-08-31T13:40:12Z
dateModified 2021-08-28T02:23:09Z
datePublished 2015-08-31T13:40:12Z