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.
المؤلفون الرئيسيون: | Knight, S, Akha, E, Timbs, A, Enver, T, Pettitt, A, Taylor, J, Hatton, C, Schuh, A |
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التنسيق: | Conference item |
منشور في: |
2009
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مواد مشابهة
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IDENTIFICATION OF NOVEL RECURRENT COPY NUMBER VARIATIONS BY HIGH RESOLUTION COMPARATIVE GENOME HYBRIDISATION
حسب: Schuh, A, وآخرون
منشور في: (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
حسب: Timbs, A, وآخرون
منشور في: (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
حسب: Timbs, A, وآخرون
منشور في: (2010) -
Clinical‐grade validation of whole genome sequencing reveals robust detection of low‐frequency variants and copy number alterations in CLL
حسب: Klintman, J, وآخرون
منشور في: (2018) -
Integrated analysis of copy number and loss of heterozygosity in primary breast carcinomas using high-density SNP array
حسب: Ching, H.C., وآخرون
منشور في: (2011)