<HashMap><database>EGA</database><scores/><additional><omics_type>Genomics</omics_type><study_type>Other</study_type><full_dataset_link>https://ega-archive.org/studies/EGAS00001003651</full_dataset_link><host>EGA</host><description>EGA study EGAS00001003651</description><dataset_title>MultiOMICS study of a pair of infant monozygotic twins with concordant B-cell ALL (WGBS)</dataset_title><dataset_title>MultiOMICS study of a pair of infant monozygotic twins with concordant B-cell ALL (WGS)</dataset_title><category>restricted</category><repository>EGA</repository></additional><is_claimable>false</is_claimable><name>multi-OMICs study of a pair of infant monozygotic twins with concordant B-cell ALL</name><description>B-cell acute lymphoblastic leukemia (B-cell ALL) is the most common cancer in childhood. Studying identical twins with B-cell ALL provides a unique and tractable model for deciphering the developmental timing of pre- and post-natal mutations contributing to clonal evolution. To date, this has mainly focused on major cytogenetic subgroups of childhood B-cell ALL, including MLL fusions, ETV6-RUNX1, hyperdiploidy, and BCR-ABL1. However, formal demonstration of the prenatal origin and “backtracking” the natural history of the leukemia remains understudied in “B-other”/Normal Karyotype (NK) B-cell ALL. To characterize the genetic and the epigenetic landscape of this particular leukemia subtype, we performed whole genome DNA-, B-cell receptor (BCR)-, and DNA bisulfite-sequencing on a pair of 8-month-old monozygotic twins diagnosed with concordant “B-other”/NK B-cell ALL.</description><dates><updated>2020-07-16 15:33:08</updated></dates><accession>EGAS00001003651</accession><cross_references><TAXONOMY>9606</TAXONOMY><EGA>EGAD00001005017</EGA><EGA>EGAD00001005018</EGA><EGA>EGAC00001001202</EGA></cross_references></HashMap>