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Epigenetics/genetics of the patient-derived xenografts of pediatric T-cell leukemia

We compared 12 pediatric T cell acute lymphoblastic leukemias collected at initial diagnosis and relapse with their corresponding PDX models. The analysis was performed on genomic level (whole genome sequencing (WGS), whole exome sequencing (WES), multiplex ligation probe amplification (MLPA), targeted sequencing) and the epigenetic level (DNA methylation, Assay for Transposase-Accessible Chromatin sequencing (ATAC-seq)). In sum, this study underlines the remarkable genomic stability, and for the first time documents the preservation of the epigenomic landscape in T-ALL-derived PDX models.

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
EGAD00001004459 Illumina HiSeq 2000 Illumina HiSeq 2500 NextSeq 500 164
Publications Citations
PDX models recapitulate the genetic and epigenetic landscape of pediatric T-cell leukemia.
EMBO Mol Med 10: 2018 e9443
23
Single-cell analysis of structural variations and complex rearrangements with tri-channel processing.
Nat Biotechnol 38: 2020 343-354
35
Chromatin accessibility landscape of pediatric T-lymphoblastic leukemia and human T-cell precursors.
EMBO Mol Med 12: 2020 e12104
6
Pediatric T-ALL type-1 and type-2 relapses develop along distinct pathways of clonal evolution.
Leukemia 36: 2022 1759-1768
3
Functional analysis of structural variants in single cells using Strand-seq.
Nat Biotechnol 41: 2023 832-844
8