Related Experiment Video
Updated: Aug 11, 2026

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
Published on: February 21, 2015
Detection of gene copy number changes in CGH microarrays using a spatially correlated mixture model
Philippe Broët1, Sylvia Richardson
1Faculté de Médecine, Université Paris-XI IFR69, 16 Avenue Paul Vaillant Couturier 94807 Villejuif Cedex, France. broet@vjf.inserm.fr
Motivation:
Comparative genomic hybridization array experiments that investigate gene copy number changes present new challenges for statistical analysis and call for methods that incorporate spatial dependence between sequences along the chromosome. For this purpose, we propose a novel method called CGHmix. It is based on a spatially structured mixture model with three states corresponding to genomic sequences that are either unmodified, deleted or amplified. Inference is performed in a Bayesian framework. From the output, posterior probabilities of belonging to each of the three states are estimated for each genomic sequence and used to classify them.
Results:
Using simulated data, CGHmix is validated and compared with both a conventional unstructured mixture model and with a recently proposed data mining method. We demonstrate the good performance of CGHmix for classifying copy number changes. In addition, the method provides a good estimate of the false discovery rate. We also present the analysis of a cancer related dataset.
Supplementary Information:
http://www.bgx.org.uk/papers.html
More Related Videos
Related Concept Videos
DNA Microarrays
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...

