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.

ग्रंथसूची विवरण
मुख्य लेखकों:	Knight, S, Akha, E, Timbs, A, Enver, T, Pettitt, A, Taylor, J, Hatton, C, Schuh, A
स्वरूप:	Conference item
प्रकाशित:	2009

IDENTIFICATION OF NOVEL RECURRENT COPY NUMBER VARIATIONS BY HIGH RESOLUTION COMPARATIVE GENOME HYBRIDISATION
द्वारा: Schuh, A, 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)

Clinical‐grade validation of whole genome sequencing reveals robust detection of low‐frequency variants and copy number alterations in CLL
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Correction: SNP Array Analysis Reveals Novel Genomic Abnormalities Including Copy Neutral Loss of Heterozygosity in Anaplastic Oligodendrogliomas
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Correction: SNP Array Analysis Reveals Novel Genomic Abnormalities Including Copy Neutral Loss of Heterozygosity in Anaplastic Oligodendrogliomas.
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द्वारा: Guièze, R, और अन्य
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Y MAP: a pipeline for visualization of copy number variation and loss of heterozygosity in eukaryotic pathogens
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द्वारा: Anne Tyybäkinoja, और अन्य
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Genome-wide analysis of copy number change and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density SNP arrays
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प्रकाशित: (2007)

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द्वारा: Karla de Oliveira Pelegrino, और अन्य
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Genetic Diversity of the Flavohemoprotein Gene of Giardia lamblia: Evidence for High Allelic Heterozygosity and Copy Number Variation
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Comprehensive SNP array study of frequently used neuroblastoma cell lines; copy neutral loss of heterozygosity is common in the cell lines but uncommon in primary tumors
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CRISPR-Cas9 globin editing can induce megabase-scale copy-neutral losses of heterozygosity in hematopoietic cells
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Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array
द्वारा: Goldstein Alisa M, और अन्य
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Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays.
द्वारा: Wang, L, और अन्य
प्रकाशित: (2008)

Microarray-based genomic analysis identifies germline and somatic copy number variants and loss of heterozygosity in acute myeloid leukaemia
द्वारा: Ambayya @ Ampiah, A Angeli, और अन्य
प्रकाशित: (2018)

Copy neutral absence of heterozygosity on chromosome 15 distal long arm: A surrogate marker for Prader–Willi/Angelman syndromes?
द्वारा: Veronica Ortega, और अन्य
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From Copy Number Identification to Copy Number Interpretation and back again
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Copy number analysis of the low-copy repeats at the primate NPHP1 locus by array comparative genomic hybridization
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Normalization of array-CGH data: influence of copy number imbalances
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Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays
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High-resolution array copy number analyses for detection of deletion, gain, amplification and copy-neutral LOH in primary neuroblastoma tumors: Four cases of homozygous deletions of the CDKN2A gene
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Mapping recurrent mosaic copy number variation in human neurons
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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.

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