home > biosample > SAMN01906001
identifier SAMN01906001
type biosample
sameAs
sra-sample　 SRS449756
organism 9606
attributes
gap_accession　 phs000553
submitter handle　 Rare_Pediatric_Phenotypes
biospecimen repository　 Rare_Pediatric_Phenotypes
study name　 Familial Exome Sequencing in Rare Pediatric Phenotypes
study design　 Family/Twin/Trios
biospecimen repository sample id　 S2
submitted sample id　 S2
submitted subject id　 x2
gap_sample_id　 915365
gap_subject_id　 706659
sex　 female
study disease　 Mendelian
body site　 Blood
histological type　 Whole blood leukocytes
analyte type　 DNA
is tumor　 No
subject is affected　 Yes
molecular data type　 SNP Genotypes (Array)
gap_consent_code　 1
gap_consent_short_name　 GRU-MDS
properties　▽ 
{...}
dbXrefs
bioproject　 PRJNA177192
sra-run　 SRR907621
sra-submission　 SRA091298
sra-study　 SRP026145
sra-sample　 SRS449756
sra-experiment　 SRX309643
distribution JSONJSON-LD
Download
biosample_set.xml.gz　 HTTPS FTP
status public
visibility controlled-access
dateCreated 2013-01-26T01:28:23Z
dateModified 2019-07-03T19:12:23Z
datePublished 2013-01-26T01:28:23Z