Skip to content
New issue

Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.

By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.

Already on GitHub? Sign in to your account

Question about euploid samples #28

Open
emanuelavilla opened this issue Sep 9, 2024 · 1 comment
Open

Question about euploid samples #28

emanuelavilla opened this issue Sep 9, 2024 · 1 comment

Comments

@emanuelavilla
Copy link

Hello!
Thanks for this interesting tool!

I have a question for you: I could not well understand from the paper if the tool could work for diploid cells (for example I am working on scATAC-Seq data from pre-leukemic murine cells).

Thanks

@thek71
Copy link
Collaborator

thek71 commented Sep 9, 2024

Hi,

in the paper we have a examples of different diploid samples (brain, bone marrow and PBMCs) that epiAneufinder should not have identified CNVs.
What we did find and report in the paper is that there where actually no CNVs found, just some random noise.
Based on the above, we conclude that epiAneufinder manages to identify diploid samples as such.

Best,
Katia

Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment
Labels
None yet
Projects
None yet
Development

No branches or pull requests

2 participants