| Literature DB >> 35622326 |
Anne Langlois de Septenville1, Myriam Boudjoghra1, Clotilde Bravetti1,2, Marine Armand1,2, Mikaël Salson3, Mathieu Giraud3, Frederic Davi4,5.
Abstract
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.Entities:
Keywords: Chronic lymphocytic leukemia; Immunoglobulin genes; Mutational status; Next generation sequencing; Somatic hypermutation analysis
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Year: 2022 PMID： 35622326 DOI： 10.1007/978-1-0716-2115-8_10
Source DB: PubMed Journal: Methods Mol Biol ISSN： 1064-3745