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Article

High-throughput genomic analysis in Waldenström's macroglobulinemia.

Clinical lymphoma, myeloma & leukemia - 1 Feb 2011

Poulain Stéphanie, Braggio Esteban, Roumier Christophe, Aijjou Rachid, Broucqsault Natacha, Galiègue-Zouitina Sylvie, Manier Salomon, Soenen Valérie, Nibourel Olivier, Duthilleul Patrick, Fonseca Rafael, Leleu Xavier

Abstract excerpt

Single-nucleotide polymorphism array (SNPa) and array-based comparative genomic hybridization (aCGH) are among the most sensitive genomic high-throughput screening techniques used in the exploration of genetic abnormalities in Waldenström's macroglobulinemia (WM). SNP and aCGH allow the identification of copy number abnormalities (CNA) at the kilobase level thus identifying cryptic genetic abnormalities unseen by...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 21454205
DOI: 10.3816/CLML.2011.n.021

Genes

TNFAIP3
TRAF3

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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