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

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

Bibliographic Details
Main Authors:	Schuh, A, Knight, S, SadighiAkha, E, Enver, T, Taylor, J
Format:	Conference item
Published:	2009

Similar Items

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.
by: Knight, S, et al.
Published: (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
by: Timbs, A, et al.
Published: (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
by: Timbs, A, et al.
Published: (2010)

SW-ARRAY: a dynamic programming solution for the identification of copy number changes in genomic DNA using array comparative genome hybridisation data
by: Price, T, et al.
Published: (2005)

Profiling of DNA Copy Number Microaberrations Associated with Congenital Disorders Among Malaysian Children Using Array Comparative Genomic Hybridisation
by: Kharuddin, Fatim
Published: (2010)

Elusive copy number variation in the mouse genome.
by: Agam, A, et al.
Published: (2010)

High-resolution genomic profiling of myelodysplasia (MDS) by microarray comparative genomic hybridisation (CGH)
by: Esoof, N, et al.
Published: (2005)

Mapping copy number variation by population-scale genome sequencing
by: Handsaker, Robert E.
Published: (2020)

Mapping copy number variation by population-scale genome sequencing.
by: Mills, R, et al.
Published: (2011)

From Copy Number Identification to Copy Number Interpretation and back again
by: Hehir-Kwa, J, et al.
Published: (2012)

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
by: Montanucci, L, et al.
Published: (2023)

Copy number variation in common disease.
by: Brand, O, et al.
Published: (2011)

SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data.
by: Price, T, et al.
Published: (2005)

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder.
by: Newbury, D, et al.
Published: (2013)

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder
by: Newbury, D, et al.
Published: (2013)

Gene copy number variations in adaptive evolution: the genomic distribution of gene copy number variations revealed by genetic mapping and their adaptive role in an undomesticated species, white spruce (Picea glauca)
by: Prunier, J, et al.
Published: (2017)

Burden of copy number variation in common variable immunodeficiency
by: Keller, M, et al.
Published: (2014)

Burden of copy number variation in common variable immunodeficiency.
by: Keller, M, et al.
Published: (2014)

Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders
by: D'Abate, L, et al.
Published: (2019)

Bayesian Nonparametric Hidden Markov Models with application to the analysis of copy-number-variation in mammalian genomes.
by: Yau, C, et al.
Published: (2008)

Bayesian Nonparametric Hidden Markov Models with application to the analysis of copy-number-variation in mammalian genomes.
by: Yau, C, et al.
Published: (2011)

Interrogation of genomes by molecular copy-number counting (MCC).
by: Daser, A, et al.
Published: (2006)

TARDBP in amyotrophic lateral sclerosis: identification of a novel variant but absence of copy number variation.
by: Bäumer, D, et al.
Published: (2009)

Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease.
by: Aldhous, Marian C., et al.
Published: (2010)

Quantification of subclonal distributions of recurrent genomic aberrations in paired pre-treatment and relapse samples from patients with B-cell chronic lymphocytic leukemia.
by: Knight, S, et al.
Published: (2012)

Quantification of subclonal distributions of recurrent genomic aberrations in paired pre-treatment and relapse samples from patients with B-cell chronic lymphocytic leukemia.
by: Knight, S, et al.
Published: (2012)

Aneuploidy and recombination in the human preimplantation embryo. Copy number variation analysis and genome-wide polymorphism genotyping
by: Konstantinidis, M, et al.
Published: (2019)

Large mosaic copy number variations confer autism risk
by: Sherman, Maxwell A, et al.
Published: (2022)

Clinical significance of de novo and inherited copy-number variation.
by: Vulto-van Silfhout, A, et al.
Published: (2013)

Clinical Significance of De Novo and Inherited Copy-Number Variation
by: Vulto-van Silfhout, A, et al.
Published: (2013)

Certified copy of resolutions
by: Cork County Association, CCA

Development of copy number assays for detection and surveillance of piperaquine resistance associated plasmepsin 2/3 copy number variation in Plasmodium falciparum
by: Ansbro, MR, et al.
Published: (2020)

Whole-genome sequencing reveals high complexity of copy number variation at insecticide resistance loci in malaria mosquitoes.
by: Lucas, E, et al.
Published: (2019)

Identification and characterization of copy number variations (CNVs) in dengue patients and its impact with vascular leakage / Zuraihan Zakaria
by: Zakaria, Zuraihan
Published: (2016)

Identification and characterization of copy number variations (CNVs) in dengue patients and its impact with vascular leakage / Zuraihan Zakaria
by: Zakaria, Zuraihan
Published: (2016)

Copy number variation of KIR genes influences HIV-1 control
by: Pelak, K, et al.
Published: (2011)

Global diversity, population stratification, and selection of human copy-number variation
by: Sudmant, P, et al.
Published: (2015)

Identification of copy number alterations by array comparative genomic hybridization in patients with late chronic or accelerated phase chronic myeloid leukemia treated with imatinib mesylate
by: Nadarajan, V.S., et al.
Published: (2011)

Gene copy number variation in natural populations of Plasmodium falciparum in Eastern Africa
by: Simam, J, et al.
Published: (2018)

Functional impact of global rare copy number variation in autism spectrum disorders.
by: Pinto, D, et al.
Published: (2010)