{"database":"EGA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"dataset_type":["Illumina HiSeq 2500;"],"full_dataset_link":["https://ega-archive.org/datasets/EGAD00001000727"],"sample_count":["38"],"description":["EGA dataset EGAD00001000727"],"repository":["EGA"],"title":["Targeted resequencing of Acute Myeloid Leukemia patients with an acquired inv(3)(q21q26) or t(3;3)(q21;q26)."],"name_synonyms":["Vasp, hemophilia, hemophilia A, DmelCG15112, ENHANCER OF ATNSI ACTIVITY, classical hemophilia, classic hemophilia, factor 8 deficiency, Data Set, autosomal haemophilia a, 2-hydroxyethyl methacrylate, NDPP1, F8C, F8B, AHF., Haemophilia A, haemophilia A, l(2)02029, enb, hem A, FVIII, VASP, classic haemophilia, DXS1253E, congenital, Historesin, 2-propenoic acid, MENA, HEMA, classic, 2-methyl-, Enb, ENA, Ena, autosomal hemophilia a, CG15112, 2-hydroxyethyl ester, glycol methacrylate, classical haemophilia, ENA/VASP"],"description_synonyms":["leukemia, Engrailed/Invected, Mds1-Evi1, PRDM3, NPH2, Data Set, acute non lymphoblastic leukemia, CMKBR7, Jbo, CCR7, Client, not genetically inherited, Mds, in, acute non lymphoblastic leukaemia, CC-CKR-7, er, IV, xEvi-1, IX14, chemokine receptor CCR7, MDS1, Mds1, MIP-3 beta receptor, acute myeloid, evi-1, acute myeloid leukaemia (AML), C-C CKR-7, CD197, AML1-EVI-1, EBI1, mecom, evi1-B, FOCUS, GP63, susceptibility to, INV, Inv, CDw197, AW455512, CCR-7, NPHP2, Evi1, EVI1, Ebi1h, D630039M04Rik, Evi-1, EBV-induced G-protein coupled receptor 1., CG17835, Znfpr1b1, acute myeloid leukemia (AML), Patient, AI428552, MSP, Clients, inv, epstein-Barr virus-induced G-protein coupled receptor 1, MDS1-EVI1, Prdm3, BLR2, evi1, Nphp2, DmelCG17835, acute myelogenous"],"additional_accession":[]},"is_claimable":false,"name":"ena-DATASET-ERASMUSMC-HEMA-27-01-2014-00:25:00:919-101 - samples","description":"Targeted resequencing on the specific regions chr3:126036241-130672290 and chr3:157712147-175694147 in hg19 centered on the chromosomal regions 3q21 and 3q26 respectively. The focus lies on the detection of the exact breakpoints in Acute Myeloid Leukemia (AML) patients having acquired a inv(3)(q21q26) or t(3;3)(q21;q26). This dataset contains all information to detect all structural variants contained within these regions, including the 3q-aberrations inducing the overexpression of the proto-oncogene EVI1.","dates":{"updated":"2017-07-26 15:39:25"},"accession":"EGAD00001000727","cross_references":{"TAXONOMY":["9606"],"EGA":["EGAC00001000162","EGAS00001000669"]}}