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.

Míreanna comhchosúla

• IDENTIFICATION OF NOVEL RECURRENT COPY NUMBER VARIATIONS BY HIGH RESOLUTION COMPARATIVE GENOME HYBRIDISATION
  de réir: Schuh, A, 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)
• Clinical‐grade validation of whole genome sequencing reveals robust detection of low‐frequency variants and copy number alterations in CLL
  de réir: Klintman, J, et al.
  Foilsithe / Cruthaithe: (2018)
• Integrated analysis of copy number and loss of heterozygosity in primary breast carcinomas using high-density SNP array
  de réir: Ching, H.C., et al.
  Foilsithe / Cruthaithe: (2011)