Dear all,
I would like to ask for a suggestion on whether I could fit a CNA profile of a sample that I do have to known CNV signatures.
I have used the package sigminer, that seems to focus entirely on CNV signature discovery nowadays, and not on fitting of a sample CNV to known CNV profiles (that are listed on https://cancer.sanger.ac.uk/signatures/cn/)
Given the data in the format :
*Chromosome Start.bp End.bp modal_cn minor_cn sample
1 chr1 1439593 2042815 3 1 EA5040545.EA5040598
2 chr1 2425333 5924715 1 0 EA5040545.EA5040598*
which package shall I use in the order to find the proxy of my sample to known CNA signatures ?
Thanks a lot,
Bogdan
HI Vincent,
thank you for your suggestions.I came across SigMIner https://shixiangwang.github.io/sigminer-book/analysis-supps.html ; documentation can be also found on the page : https://github.com/ShixiangWang/sigminer
I am testing it now to check whether it fits our needs.
Thanks so much,
~ Bogdan
copy that - good luck