Detection of Rare Germline Variants in the Genomes of Patients with B-Cell Neoplasms

There is growing evidence indicating the implication of germline variation in cancer predisposition and prognostication. Here, we describe an analysis of likely disruptive rare variants across the genomes of 726 patients with B-cell lymphoid neoplasms. We discovered a significant enrichment for two...

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Veröffentlicht in:Cancers 2021-03, Vol.13 (6), p.1340
Hauptverfasser: Mosquera Orgueira, Adrián, Cid López, Miguel, Peleteiro Raíndo, Andrés, Díaz Arias, José Ángel, Antelo Rodríguez, Beatriz, Bao Pérez, Laura, Alonso Vence, Natalia, Bendaña López, Ángeles, Abuin Blanco, Aitor, Melero Valentín, Paula, Ferreiro Ferro, Roi, Aliste Santos, Carlos, Fraga Rodríguez, Máximo Francisco, González Pérez, Marta Sonia, Pérez Encinas, Manuel Mateo, Bello López, José Luis
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Sprache:eng
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