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