ArticleBMC genomics2009
CGHnormaliter: an iterative strategy to enhance normalization of array CGH data with imbalanced aberrations.
Article in BMC genomics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Integrating copy number data of 64 iAMP21 BCP-ALL patients narrows the common region of amplification to 1.57 Mb.Frontiers in oncology · 2023Article
- High STAP1 expression in DUX4-rearranged cases is not suitable as therapeutic target in pediatric B-cell precursor acute lymphoblastic leukemia.Scientific reports · 2018Article
- Tyrosine kinase fusion genes in pediatric BCR-ABL1-like acute lymphoblastic leukemia.Oncotarget · 2017Article
- Genome instability model of metastatic neuroblastoma tumorigenesis by a dictionary learning algorithm.BMC medical genomics · 2015Article
- Impact of centralization on aCGH-based genomic profiles for precision medicine in oncology.Annals of oncology : official journal of the European Society for Medical Oncology · 2015Article
- PAIR: paired allelic log-intensity-ratio-based normalization method for SNP-CGH arrays.Bioinformatics (Oxford, England) · 2013Article
- A high-throughput computational framework for identifying significant copy number aberrations from array comparative genomic hybridisation data.Advances in bioinformatics · 2012Article
- Single-cell copy number variation detection.Genome biology · 2011Article
- aCGH.Spline--an R package for aCGH dye bias normalization.Bioinformatics (Oxford, England) · 2011Article
- A critical assessment of cross-species detection of gene duplicates using comparative genomic hybridization.BMC genomics · 2010Article
- Multiplex Amplicon Quantification (MAQ), a fast and efficient method for the simultaneous detection of copy number alterations in neuroblastoma.BMC genomics · 2010Article
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5 authors.
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Abstract
backgroundArray comparative genomic hybridization (aCGH) is a popular technique for detection of genomic copy number imbalances. These play a critical role in the onset of various types of cancer. In the analysis of aCGH data, normalization is deemed a critical pre-processing step. In general, aCGH normalization approaches are similar to those used for gene expression data, albeit both data-types differ inherently. A particular problem with aCGH data is that imbalanced copy numbers lead to improper normalization using conventional methods.
resultsIn this study we present a novel method, called CGHnormaliter, which addresses this issue by means of an iterative normalization procedure. First, provisory balanced copy numbers are identified and subsequently used for normalization. These two steps are then iterated to refine the normalization. We tested our method on three well-studied tumor-related aCGH datasets with experimentally confirmed copy numbers. Results were compared to a conventional normalization approach and two more recent state-of-the-art aCGH normalization strategies. Our findings show that, compared to these three methods, CGHnormaliter yields a higher specificity and precision in terms of identifying the 'true' copy numbers.
conclusionWe demonstrate that the normalization of aCGH data can be significantly enhanced using an iterative procedure that effectively eliminates the effect of imbalanced copy numbers. This also leads to a more reliable assessment of aberrations. An R-package containing the implementation of CGHnormaliter is available at http://www.ibi.vu.nl/programs/cghnormaliterwww.
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