Question: computing the CNA in the cancer genomes
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gravatar for Bogdan
10 months ago by
Bogdan800
Palo Alto, CA, USA
Bogdan800 wrote:

Dear all, please may I ask for your opinion :

when analyzing the somatic Copy Number Alterations (CNA) in the cancer genomes (based on whole genome sequencing data), would you recommend using (running) the CNA_calling algorithm :

-- per EACH CHROMOSOME individually, or

-- on ALL CHROMOSOMES at the same time (on a genome-wide scale) ?

I am asking because multiple copies of a chromosome may potentially introduce biases when computing the baseline corresponding to the diploid status of the genome. Thank you !

-- bogdan

cancer cnv copy number cna • 408 views
ADD COMMENTlink modified 10 months ago by Kevin Blighe45k • written 10 months ago by Bogdan800
0
gravatar for Kevin Blighe
10 months ago by
Kevin Blighe45k
Kevin Blighe45k wrote:

Dear Bogdan, as far as I am aware, ASCAT calculates allele-specific somatic copy number events while adjusting for tumour ploidy.

Kevin

ADD COMMENTlink written 10 months ago by Kevin Blighe45k
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