ID   HPSI0713i-foop_1
AC   CVCL_AG54
SY   WTSIi067-A
DR   BioSamples; SAMEA2399242
DR   EBiSC; WTSIi067-A
DR   ECACC; 66540133
DR   ECACC; 77650097
DR   HipSci; HPSI0713i-foop_1
DR   hPSCreg; WTSIi067-A
DR   SKIP; SKIP002655
DR   Wikidata; Q54891246
RX   PubMed=28489815;
CC   From: Cambridge BioResource; Cambridge; United Kingdom.
CC   From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom.
CC   Omics: Genomics; DNA methylation analysis.
CC   Omics: Genomics; Whole exome sequencing.
CC   Omics: Transcriptomics; Microarray.
CC   Omics: Transcriptomics; RNAseq.
CC   Discontinued: ECACC; 66540133; true.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_AG55 ! HPSI0713i-foop_2
OI   CVCL_JP32 ! HPSI0713i-foop_3
SX   Female
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 23-02-16; Last updated: 10-04-25; Version: 14
//
RX   PubMed=28489815; DOI=10.1038/nature22403; PMCID=PMC5524171;
RA   Kilpinen H., Goncalves A., Leha A., Afzal V., Alasoo K., Ashford S.,
RA   Bala S., Bensaddek D., Casale F.P., Culley O.J., Danecek P.,
RA   Faulconbridge A., Harrison P.W., Kathuria A., McCarthy D.,
RA   McCarthy S.A., Meleckyte R., Memari Y., Moens N., Soares F., Mann A.,
RA   Streeter I., Agu C.A., Alderton A., Nelson R., Harper S., Patel M.J.,
RA   White A., Patel S.R., Clarke L., Halai R., Kirton C.M.,
RA   Kolb-Kokocinski A., Beales P., Birney E., Danovi D., Lamond A.I.,
RA   Ouwehand W.H., Vallier L., Watt F.M., Durbin R., Stegle O.,
RA   Gaffney D.J.;
RT   "Common genetic variation drives molecular heterogeneity in human
RT   iPSCs.";
RL   Nature 546:370-375(2017).
//