New versatile genetic test for lymphoid neoplasms supports personalized management of patients and further research (IMAGE)

Elsevier

New versatile genetic test for lymphoid neoplasms supports personalized management of patients and further research

Caption

A schematic presentation of genomic targets and molecular markers integrated within the LYmphoid NeXt-generation sequencing (LYNX) panel design for the most common lymphoid malignant tumors (1 chronic lymphocytic leukemia, 2 mantle cell lymphoma, 3 follicular lymphoma, 4 diffuse large B-cell lymphoma, 5 acute lymphoblastic leukemia, and 6 Philadelphia chromosome–like acute lymphoblastic leukemia). cnLOH, copy neutral loss of heterozygosity; CNV, copy number variant; SNP, single-nucleotide polymorphism.

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The Journal of Molecular Diagnostics

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