Genome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays

We describe a method for automatic detection of absolute segmental copy numbers and genotype status in complex cancer genome profiles measured with single-nucleotide polymorphism (SNP) arrays. The method is based on pattern recognition of segmented and smoothed copy number and allelic imbalance prof...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Popova, Tatiana, Manié, Elodie, Stoppa-Lyonnet, Dominique, Rigaill, Guillem, Barillot, Emmanuel, Stern, Marc Henri
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2009
Aiheet:
Method
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2810663/
https://ncbi.nlm.nih.gov/pubmed/19903341
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2009-10-11-r128
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