EGAGenomicsIllumina HiSeq 2000Cancer Genomicshttps://ega-archive.org/studies/EGAS00001000033EGAEGA study EGAS00001000033Fanconi Anemia transformation to AMLEGArestrictedRunx-1, aml, leukemia, Acute myelogenous leukemia, Fanconi anemia, Leukemia, pancytopenia, Fanconi's Anemia, acute non lymphoblastic leukemia, Myeloid, Myeloblastic, Xaml1, Fanconi Pancytopenia, Acute Myeloblastic Leukemia, Fanconi's anemia, susceptibility to, Fanconi pancytopenia, Acute Myeloid Leukemia, aml1., primary erythroid hypoplasia, amlcr1, pebp2ab, Fanconi Panmyelopathy, Fanconi panmyelopathy, AML, XAML, Fanconi Anemias, Anemia, Acute, Panmyelopathy, acute non lymphoblastic leukaemia, Anemias, congenital, Fanconi, aml-1, Fanconi Hypoplastic Anemia, Fanconi's, ANLL, acute myeloid, aml1-evi-1, Fanconi's anaemia, cbfa2, evi-1, FA, acute myelogenousMyelogenous Leukemias, Myelocytic, Acute Myeloblastic, PS, acute myeloblastic leukemia, human being, Materials, nj42, Nonlymphocytic Leukemia, beta-PS, acute non lymphoblastic leukemia, Myeloid, popliteal pterygium syndrome, acute myeloblastic leukaemia, olfC, acute myelogenous leukaemia, Neoplasms, Fanconi's anemia, Fanconi pancytopenia, number, Benign Neoplasm, Myelocytic Leukemia, Gene, beta-Int, CG1560, broad, multiple pterygium syndrome, Tumor, Bartsocas-Papas type, Malignant, presence, Acute Myeloid, gDNA, Acute Myelocytic Leukemias, Human, Mys, acute non lymphoblastic leukaemia, Homo sapiens, beta[[PS]]-integrin, congenital, Fanconi, PSbeta, Acute Myelocytic, Acute Nonlymphoblastic, acute myeloid, betaPS-integrin, Myeloblastic Leukemia, Man, BC, Leukemia, Man (Taxonomy), Genetic, Fanconi's Anemia, Genomes, Malignancy, BetaPS-Int, Acute Myelogenous, Acute Myeloblastic Leukemia, BCs, Myelogenous Leukemia, beta-integrin, MAb6G11, Acute Nonlymphocytic Leukemias, l(1)mys, betamys, Fanconi panmyelopathy, beta[[P]]S, Acute Myeloid Leukemia without Maturation, Neoplasias, l(1)7Dn, Acute Nonlymphoblastic Leukemia, l(1)7Db, Acute Nonlymphocytic Leukemia, Anemias, malignant neoplasm, Myeloid Leukemia, Myelocytic Leukemias, CG7659, integrin beta[[PS]], Fanconi's, ANLL, Malignancies, Nonlymphoblastic Leukemias, BetaPS, l(1)G0281, popliteal, HHT1, acute myelogenous, Cancer, Tumors, leukemia, Myelogenous, Tap, Fanconi anemia, M1, M2, acute myelogenous leukemia, wide/broad, Malignant Neoplasm, pterygium popliteal lethal type, Edg, bHLHc9, Modern, betaPS1, popliteal pterygium syndrome lethal type, primary erythroid hypoplasia, Cistrons, Leukemias, Fanconi Panmyelopathy, AML, Acute Myelocytic Leukemia, Nonlymphoblastic Leukemia, Nonlymphocytic Leukemias, DmelCG1560, betaPS Int, count in organism, Anemia, Nonlymphoblastic, MT, Benign, Acute Myeloid Leukemias, Myeloid Leukemias, lethal type, Fanconi Hypoplastic Anemia, Neoplasm, Genetic Materials, l(1)EM28, b[[PS]], Acute Nonlymphocytic, END, Library, FA, Genetic Material, Acute Myelogenous Leukemia, l(1)G0233, acute, Acute myelogenous leukemia, DmelCG7659, BPS, primary cancer, CT40473, pancytopenia, Myeloblastic, Fanconi Pancytopenia, EM28, l(1)968, susceptibility to, Myeloblastic Leukemias, pterygium, l(1)DA551, betaInt, Acute Myeloid Leukemia, acute myeloid leukemia, Benign Neoplasms, beta1, acute myeloid leukaemia, INSDC_feature:gene, whole genome, Cancers, Nonlymphocytic, malignant tumor, human, Malignant Neoplasms, beta[[PS]], Fanconi Anemias, Acute Myeloid Leukemia with Maturation, BPs, bps, beta[[mys]], bPS, wide, Acute, Panmyelopathy, l(1)93p, Acute Nonlymphoblastic Leukemias, Material, Acute Myeloblastic Leukemias, Modern Man, cardinality, Acute Myelogenous Leukemias, betaPS, Cistron, beta-int, PS[[beta]], Genetic Material., Fanconi's anaemia, ORW1, l(3)01658, AML - acute Myeloid Leukemia, Neoplasia, Aslan typefalse1 Fanconi Anemia transformation to AMLGenomic libraries (500 bps) will be generated from total genomic DNA derived from 7 Fanconi anemia (FA) derived Acute myeloid leukemia samples and subjected to total of two lanes of 50 bp, paired end sequencing on the llumina HiSeq. Paired reads will be mapped to build 37 of the human reference genome to facilitate the generation of genome wide copy number information, and the identification of novel rearranged cancer genes and gene fusions.2017-07-26 15:39:24EGAS000010000339606EGAD00001000072EGAC00001000000