ID   GM18516
AC   CVCL_P463
DR   CLO; CLO_0024892
DR   Coriell; GM18516
DR   GEO; GSM112581
DR   GEO; GSM112885
DR   GEO; GSM188861
DR   GEO; GSM273461
DR   GEO; GSM291718
DR   GEO; GSM315148
DR   GEO; GSM485466
DR   GEO; GSM485431
DR   GEO; GSM485482
DR   GEO; GSM485416
DR   GEO; GSM649225
DR   GEO; GSM649861
DR   GEO; GSM1164206
DR   GEO; GSM1164216
DR   GEO; GSM1164226
DR   GEO; GSM1164236
DR   GEO; GSM1164246
DR   GEO; GSM1204878
DR   GEO; GSM1719851
DR   IGSR; NA18516
DR   PRIDE; PXD000419
DR   PRIDE; PXD001406
DR   Wikidata; Q54849592
RX   PubMed=17122850;
RX   PubMed=19043577;
RX   PubMed=19797678;
RX   PubMed=20220758;
RX   PubMed=21397061;
RX   PubMed=24136357;
RX   PubMed=24136359;
CC   Part of: International Genome Sample Resource (1000 genomes project) cell lines.
CC   Population: African; Yoruba in Ibadan, Nigeria (YRI).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Omics: CNV analysis.
CC   Omics: Deep proteome analysis.
CC   Omics: Genome sequenced.
CC   Omics: H3K27ac ChIP-seq epigenome analysis.
CC   Omics: H3K27me3 ChIP-seq epigenome analysis.
CC   Omics: H3K4me1 ChIP-seq epigenome analysis.
CC   Omics: H3K4me3 ChIP-seq epigenome analysis.
CC   Omics: Transcriptome analysis by microarray.
CC   Omics: Transcriptome analysis by RNAseq.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Age unspecified
CA   Transformed cell line
DT   Created: 05-11-13; Last updated: 30-01-24; Version: 18
//
RX   PubMed=17122850; DOI=10.1038/nature05329;
RA   Redon R., Ishikawa S., Fitch K.R., Feuk L., Perry G.H., Andrews T.D.,
RA   Fiegler H., Shapero M.H., Carson A.R., Chen W.-W., Cho E.K., Dallaire S.,
RA   Freeman J.L., Gonzalez J.R., Gratacos M., Huang J., Kalaitzopoulos D.,
RA   Komura D., MacDonald J.R., Marshall C.R., Mei R., Montgomery L.,
RA   Nishimura K., Okamura K., Shen F., Somerville M.J., Tchinda J.,
RA   Valsesia A., Woodwark C., Yang F.-T., Zhang J.-J., Zerjal T., Zhang J.,
RA   Armengol L., Conrad D.F., Estivill X., Tyler-Smith C., Carter N.P.,
RA   Aburatani H., Lee C., Jones K.W., Scherer S.W., Hurles M.E.;
RT   "Global variation in copy number in the human genome.";
RL   Nature 444:444-454(2006).
//
RX   PubMed=19043577; DOI=10.1371/journal.pgen.1000287;
RA   Choy E., Yelensky R., Bonakdar S., Plenge R.M., Saxena R.,
RA   De Jager P.L., Shaw S.Y., Wolfish C.S., Slavik J.M., Cotsapas C.,
RA   Rivas M.A., Dermitzakis E.T., Cahir-McFarland E., Kieff E.D.,
RA   Hafler D.A., Daly M.J., Altshuler D.M.;
RT   "Genetic analysis of human traits in vitro: drug response and gene
RT   expression in lymphoblastoid cell lines.";
RL   PLoS Genet. 4:E1000287-E1000287(2008).
//
RX   PubMed=19797678; DOI=10.1101/gr.097600.109;
RA   Nayak R.R., Kearns M., Spielman R.S., Cheung V.G.;
RT   "Coexpression network based on natural variation in human gene
RT   expression reveals gene interactions and functions.";
RL   Genome Res. 19:1953-1962(2009).
//
RX   PubMed=20220758; DOI=10.1038/nature08872;
RA   Pickrell J.K., Marioni J.C., Pai A.A., Degner J.F., Engelhardt B.E.,
RA   Nkadori E., Veyrieras J.-B., Stephens M., Gilad Y., Pritchard J.K.;
RT   "Understanding mechanisms underlying human gene expression variation
RT   with RNA sequencing.";
RL   Nature 464:768-772(2010).
//
RX   PubMed=21397061; DOI=10.1016/j.ajhg.2011.02.004;
RA   Campbell C.D., Sampas N., Tsalenko A., Sudmant P.H., Kidd J.M.,
RA   Malig M., Vu T.H., Vives L., Tsang P., Bruhn L., Eichler E.E.;
RT   "Population-genetic properties of differentiated human copy-number
RT   polymorphisms.";
RL   Am. J. Hum. Genet. 88:317-332(2011).
//
RX   PubMed=24136357; DOI=10.1126/science.1242379;
RA   Khan Z., Ford M.J., Cusanovich D.A., Mitrano A., Pritchard J.K.,
RA   Gilad Y.;
RT   "Primate transcript and protein expression levels evolve under
RT   compensatory selection pressures.";
RL   Science 342:1100-1104(2013).
//
RX   PubMed=24136359; DOI=10.1126/science.1242429;
RA   McVicker G., van de Geijn B., Degner J.F., Cain C.E., Banovich N.E.,
RA   Raj A., Lewellen N., Myrthil M., Gilad Y., Pritchard J.K.;
RT   "Identification of genetic variants that affect histone modifications
RT   in human cells.";
RL   Science 342:747-749(2013).
//