Quantification of subclonal distributions of recurrent genomic aberrations in paired pre-treatment and relapse samples from patients with B-cell chronic lymphocytic leukemia.
Genome-wide array approaches and sequencing analyses are powerful tools for identifying genetic aberrations in cancers, including leukemias and lymphomas. However, the clinical and biological significance of such aberrations and their subclonal distribution are poorly understood. Here, we present th...
Main Authors: | Knight, S, Yau, C, Clifford, R, Timbs, A, Sadighi Akha, E, Dréau, H, Burns, A, Ciria, C, Oscier, D, Pettitt, A, Dutton, S, Holmes, C, Taylor, J, Cazier, J, Schuh, A |
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Format: | Journal article |
Sprog: | English |
Udgivet: |
2012
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Lignende værker
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Quantification of subclonal distributions of recurrent genomic aberrations in paired pre-treatment and relapse samples from patients with B-cell chronic lymphocytic leukemia.
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Identification of Novel Recurrent Copy Number Variations and Regions of Copy-Neutral Loss of Heterozygosity by High Resolution Genomic Array in Pre-Treatment and Relapsed B-CLL.
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Quantitative Whole Genome Analysis of Sequential Samples From Patients with B-CLL Identifies Novel Recurrent Copy Number Alterations Involving Critical B-Cell Transcription Factors
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Quantitative Whole Genome Analysis of Sequential Samples From Patients with B CLL Identifies Novel Recurrent Copy Number Alterations Involving Critical B Cell Transcription Factors
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Evolution and Impact of Subclonal Mutations in Chronic Lymphocytic Leukemia
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