IDENTIFICATION OF NOVEL RECURRENT COPY NUMBER VARIATIONS BY HIGH RESOLUTION COMPARATIVE GENOME HYBRIDISATION
Prif Awduron: | Schuh, A, Knight, S, SadighiAkha, E, Enver, T, Taylor, J |
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Fformat: | Conference item |
Cyhoeddwyd: |
2009
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Eitemau Tebyg
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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.
gan: Knight, S, et al.
Cyhoeddwyd: (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
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Cyhoeddwyd: (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
gan: Timbs, A, et al.
Cyhoeddwyd: (2010) -
A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation
gan: Karimpour-Fard Anis, et al.
Cyhoeddwyd: (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
gan: Price, T, et al.
Cyhoeddwyd: (2005)