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GAP | A tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays

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A method for automatic detection of absolute segmental copy numbers and genotype status in complex cancer genome profiles measured by SNP arrays.

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GAP forum

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GAP classification

GAP specifications

Unique identifier:
OMICS_02119
Software type:
Package/Module
Restrictions to use:
None
Computer skills:
Advanced
Maintained:
Yes
Name:
Genome Alteration Print
Interface:
Command line interface
Operating system:
Unix/Linux
Stability:
Stable

GAP distribution

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No versioning.

Credits

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Publications

Institution(s)

Centre de Recherche, Institut Curie, Paris, France

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