ID HG00278 AC CVCL_P799 DR ArrayExpress; E-GEUV-1 DR ArrayExpress; E-GEUV-2 DR ArrayExpress; E-GEUV-3 DR BioSamples; SAME123425 DR Coriell; HG00278 DR GEO; GSM649627 DR GEO; GSM1718183 DR IGSR; HG00278 DR Wikidata; Q54883448 RX PubMed=21397061; RX PubMed=24037378; RX PubMed=27617755; CC Part of: International Genome Sample Resource (1000 genomes project) cell lines. CC Population: Caucasian; Finnish in Finland (FIN). CC Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV). CC Omics: Genomics; Whole genome sequencing. CC Omics: Transcriptomics; RNAseq. CC Omics: Variations; CNV analysis. 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: 10-04-25; Version: 16 // RX PubMed=21397061; DOI=10.1016/j.ajhg.2011.02.004; PMCID=PMC3059424; 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=24037378; DOI=10.1038/nature12531; PMCID=PMC3918453; RA Lappalainen T., Sammeth M., Friedlander M.R., 't Hoen P.A.C., RA Monlong J., Rivas M.A., Gonzalez-Porta M., Kurbatova N., Griebel T., RA Ferreira P.G., Barann M., Wieland T., Greger L., van Iterson M., RA Almlof J.C., Ribeca P., Pulyakhina I., Esser D., Giger T., Tikhonov A., RA Sultan M., Bertier G., MacArthur D.G., Lek M., Lizano E., RA Buermans H.P.J., Padioleau I., Schwarzmayr T., Karlberg O., Ongen H., RA Kilpinen H., Beltran S., Gut M., Kahlem K., Amstislavskiy V., RA Stegle O., Pirinen M., Montgomery S.B., Donnelly P., McCarthy M.I., RA Flicek P., Strom T.-M., Lehrach H., Schreiber S., Sudbrak R., RA Carracedo A., Antonarakis S.E., Hasler R., Syvanen A.-C., RA van Ommen G.-J.B., Brazma A., Meitinger T., Rosenstiel P., Guigo R., RA Gut I.G., Estivill X., Dermitzakis E.T.; RG Geuvadis Consortium; RT "Transcriptome and genome sequencing uncovers functional variation in RT humans."; RL Nature 501:506-511(2013). // RX PubMed=27617755; DOI=10.1038/srep32406; PMCID=PMC5019111; RA Ferreira P.G., Oti M., Barann M., Wieland T., Ezquina S., RA Friedlander M.R., Rivas M.A., Esteve-Codina A., Rosenstiel P., RA Strom T.-M., Lappalainen T., Guigo R., Sammeth M.; RG Geuvadis Consortium; RT "Sequence variation between 462 human individuals fine-tunes RT functional sites of RNA processing."; RL Sci. Rep. 6:32406-32406(2016). //