<p>Relapse is currently the major cause of death in children with B-ALL. The goal of this study is to uncover the genetic underpinnings of relapsed B-ALL in the <a href="https://childrensoncologygroup.org/aall1331">AALL1331</a> cohort (PMID: <a href="https://pubmed.ncbi.nlm.nih.gov/33651090/">33651090</a>) via whole genome and transcriptome sequencing of matched diagnosis, relapse, and remission specimens. We aim to discover genetic alterations that drive treatment resistance in relapsed tumors. We also aim to investigate the feasibility of detecting residual tumors from remission samples with the ultimate goal to improve risk stratification using NGS-based minimal residual disease (MRD) detection. Here we only report data from patients in remission with the aim of determining MRD. We will submit corresponding data for the diagnosis and relapse components of our cohort in a future version of our study.</p>

Tracking Therapy-Resistant Alterations in Childhood Acute Lymphoblastic    Leukemia

Precursor B-Cell Lymphoblastic Leukemia-Lymphoma study with Targeted-Capture data on dbGaP (72 participants)

Tracking Therapy-Resistant Alterations in Childhood Acute Lymphoblastic Leukemia

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