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

Protein sequence abundance #13

Open
cmorganl opened this issue Jul 18, 2019 · 5 comments
Open

Protein sequence abundance #13

cmorganl opened this issue Jul 18, 2019 · 5 comments
Labels
enhancement New feature or request

Comments

@cmorganl
Copy link

Hi there,

I've just started using PLASS, specifically plass assemble, and I really like it!

This isn't an issue but a potential enhancement. I was wondering how I might be able to recover abundance information for each protein assembled. Its not as simple as with nucleotide contigs since I'm unable to align the reads back to the assembly in this case.

Could the abundance of proteins be included in the header, as SPAdes does? Alternatively, a table mapping header to its respective abundance would be convenient as well. I hope I haven't misinterpreted the output and its already provided :)

Thanks!
Connor

@martin-steinegger martin-steinegger added the enhancement New feature or request label Jul 18, 2019
@martin-steinegger
Copy link
Member

martin-steinegger commented Jul 18, 2019

Yes I would love to have this as well. 👍
But so far I did not come up with an solution how I could gather this information.

It is hard to set rules what alignments should be part of the abundance computation since plass allows to assemble similar proteins and not just exact once.

We estimated the abundance in the plass publication using the mmseqs map workflow. This workflow performs a six frame translated search and has strict mapping thresholds.

@apcamargo
Copy link

Wouldn't it possible to use an EM algorithm to "distribute" the read among its multiple hits?

@martin-steinegger
Copy link
Member

@apcamargo yes this a good idea. But do you know if EM would be fast enough to handle this large amount of data?

@apcamargo
Copy link

apcamargo commented Jul 25, 2019

I don't know. It would depend on the total amount of proteins and reads. I imagine it would be much slower than a typical RNA-Seq quantification, but not unfeasible. But that's just my impression, I've never done something like that.

@mooreryan
Copy link

I was just thinking about this as well...are there any current plans to include this in plass, or would it be better for now to try the mmseqs map workflow?

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

No branches or pull requests

4 participants