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

Ejemplares similares

• 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.
  por: Knight, S, et al.
  Publicado: (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
  por: Timbs, A, et al.
  Publicado: (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
  por: Timbs, A, et al.
  Publicado: (2010)
• SW-ARRAY: a dynamic programming solution for the identification of copy number changes in genomic DNA using array comparative genome hybridisation data
  por: Price, T, et al.
  Publicado: (2005)
• Profiling of DNA Copy Number Microaberrations Associated with Congenital Disorders Among Malaysian Children Using Array Comparative Genomic Hybridisation
  por: Kharuddin, Fatim
  Publicado: (2010)