Abstract

BackgroundChromosomal copy number changes (aneuploidies) play a key role in cancer progression and molecular evolution. These copy number changes can be studied using microarray-based comparative genomic hybridization (array CGH) or gene expression microarrays. However, accurate identification of amplified or deleted regions requires a combination of visual and computational analysis of these microarray data.ResultsWe have developed ChARMView, a visualization and analysis system for guided discovery of chromosomal abnormalities from microarray data. Our system facilitates manual or automated discovery of aneuploidies through dynamic visualization and integrated statistical analysis. ChARMView can be used with array CGH and gene expression microarray data, and multiple experiments can be viewed and analyzed simultaneously.ConclusionChARMView is an effective and accurate visualization and analysis system for recognizing even small aneuploidies or subtle expression biases, identifying recurring aberrations in sets of experiments, and pinpointing functionally relevant copy number changes. ChARMView is freely available under the GNU GPL at .

Highlights

  • Chromosomal copy number changes play a key role in cancer progression and molecular evolution

  • Methodology: statistical analysis ChARMView computational analysis automatically detects regions of non-random spatial bias and is appropriate for any genomic data associated with chromosomal coordinates

  • Statistical analysis is based on our algorithm ChARM (Chromosomal Aberration Region Miner), described in detail in [16]

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Summary

Results

We have developed ChARMView, a visualization and analysis system for guided discovery of chromosomal abnormalities from microarray data. Our system facilitates manual or automated discovery of aneuploidies through dynamic visualization and integrated statistical analysis. ChARMView can be used with array CGH and gene expression microarray data, and multiple experiments can be viewed and analyzed simultaneously

Conclusion
Background
Results and Discussion
13. Saldanha AJ
17. Fisher R
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