Immunoglobulin Gene Mutational Status Assessment by Next Generation Sequencing in Chronic Lymphocytic Leukemia
Résumé
B cell receptor (BcR) immunoglobulins (IG) display a tremendous diversity due to complex DNA rearrangements, the V(D)J recombination, further enhanced by the somatic hypermutation process. In chronic lymphocytic leukemia (CLL), the mutational load of the clonal BcR IG expressed by the leukemic cells constitutes an important prognostic and predictive biomarker. Here, we provide a reliable methodology capable of determining the mutational status of IG genes in CLL using high-throughput sequencing, starting from leukemic cell DNA or RNA.
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Requiert hal-04453057 Logiciel Aurélien Béliard, Marc Duez, Mathieu Giraud, Ryan Herbert, Tatiana Rocher, et al.. Vidjil. 2018, ⟨swh:1:dir:919b1f80b59a0d7139e816a8acd45b5139032f55;origin=https://gitlab.inria.fr/vidjil/vidjil;visit=swh:1:snp:291e56d00815773ebeae2102804ef8be5eb62b86;anchor=swh:1:rev:5d5ebe597a7271b8c4296da422de1ad81bee0804⟩. ⟨hal-04453057⟩