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

समान संसाधन

• 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.
  द्वारा: Knight, S, और अन्य
  प्रकाशित: (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
  द्वारा: Timbs, A, और अन्य
  प्रकाशित: (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
  द्वारा: Timbs, A, और अन्य
  प्रकाशित: (2010)
• A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation
  द्वारा: Karimpour-Fard Anis, और अन्य
  प्रकाशित: (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
  द्वारा: Price, T, और अन्य
  प्रकाशित: (2005)