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IDENTIFICATION OF NOVEL RECURRENT COPY NUMBER VARIATIONS BY HIGH RESOLUTION COMPARATIVE GENOME HYBRIDISATION

IDENTIFICATION OF NOVEL RECURRENT COPY NUMBER VARIATIONS BY HIGH RESOLUTION COMPARATIVE GENOME HYBRIDISATION

Bibliografiske detaljer
Main Authors: Schuh, A, Knight, S, SadighiAkha, E, Enver, T, Taylor, J
Format: Conference item
Udgivet: 2009
  • Beholdninger
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Lignende værker

  • 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.
    af: Knight, S, et al.
    Udgivet: (2009)
  • Quantitative Whole Genome Analysis of Sequential Samples From Patients with B-CLL Identifies Novel Recurrent Copy Number Alterations Involving Critical B-Cell Transcription Factors
    af: Timbs, A, et al.
    Udgivet: (2010)
  • Quantitative Whole Genome Analysis of Sequential Samples From Patients with B CLL Identifies Novel Recurrent Copy Number Alterations Involving Critical B Cell Transcription Factors
    af: Timbs, A, et al.
    Udgivet: (2010)
  • A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation
    af: Karimpour-Fard Anis, et al.
    Udgivet: (2010-08-01)
  • SW-ARRAY: a dynamic programming solution for the identification of copy number changes in genomic DNA using array comparative genome hybridisation data
    af: Price, T, et al.
    Udgivet: (2005)

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