<HashMap><database>EGA</database><scores/><additional><omics_type>Genomics</omics_type><dataset_type>N/A</dataset_type><full_dataset_link>https://ega-archive.org/datasets/EGAD00001003568</full_dataset_link><sample_count>4</sample_count><description>EGA dataset EGAD00001003568</description><repository>EGA</repository><title>Genome - MBD4-deficient AML</title><name_synonyms>Vasp, VASP, Data Set., DmelCG15112, ENHANCER OF ATNSI ACTIVITY, MENA, NDPP1, l(2)02029, Enb, enb, ENA, Ena, CG15112, ENA/VASP</name_synonyms><description_synonyms>leukemia, Antemortem Diagnoses, screening, Antemortem Diagnosis, findings, acute non lymphoblastic leukemia, Myeloid, Genome Sequencing, Diagnosis, Examination and Diagnoses, Diagnoses, AML, Postmortem, Screenings, Complete Genome, acute non lymphoblastic leukaemia, Mass Screenings, Examinations and Diagnoses, HiSeq X Ten., Mass, symptoms, Screening, acute myeloid, Antemortem, aml1-evi-1, Postmortem Diagnosis, cbfa2, evi-1, Runx-1, Diagnoses and Examination, aml, Acute myelogenous leukemia, Postmortem Diagnoses, Leukemia, Complete, Whole Genome, Genomes, Myeloblastic, Xaml1, Acute Myeloblastic Leukemia, susceptibility to, Complete Genome Sequencing, signs, Acute Myeloid Leukemia, whole genome, Diagnoses and Examinations, amlcr1, pebp2ab, aml1, Sequencing, XAML, Acute, Whole, aml-1, ANLL, Diagnose, acute myelogenous</description_synonyms></additional><is_claimable>false</is_claimable><name>ena-DATASET-WEHI-17-08-2017-10:23:29:025-405 - samples</name><description>Genome sequencing at diagnosis and post induction for WEHI-AML-1 and WEHI-AML-2. Whole genome sequencing was performed on an Illumina HiSeq X Ten.</description><dates><updated>2018-10-02 14:23:22</updated></dates><accession>EGAD00001003568</accession><cross_references><TAXONOMY>9606</TAXONOMY><EGA>EGAC00001000709</EGA><EGA>EGAS00001002581</EGA></cross_references></HashMap>