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

Míreanna comhchosúla

• 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.
  de réir: Knight, S, et al.
  Foilsithe / Cruthaithe: (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
  de réir: Timbs, A, et al.
  Foilsithe / Cruthaithe: (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
  de réir: Timbs, A, et al.
  Foilsithe / Cruthaithe: (2010)
• A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation
  de réir: Karimpour-Fard Anis, et al.
  Foilsithe / Cruthaithe: (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
  de réir: Price, T, et al.
  Foilsithe / Cruthaithe: (2005)