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

Collate notes from 4 NGS VC papers into summary+questions #3

Closed
thejmazz opened this issue May 22, 2016 · 3 comments
Closed

Collate notes from 4 NGS VC papers into summary+questions #3

thejmazz opened this issue May 22, 2016 · 3 comments
Assignees
Labels
Milestone

Comments

@thejmazz
Copy link
Member

@thejmazz thejmazz commented May 22, 2016

  • Review of alignment and SNP calling algorithms for next-generation sequencing data (Mielczarek, 2015)
  • Genotype and SNP calling from next-generation sequencing data (Nielson, 2011)
  • Best practices for evaluating single nucleotide variant calling methods for microbial genomics (Olson, 2015)
  • A survey of tools for variant analysis of next-generation genome sequencing data (Pabinger, 2012)
@thejmazz thejmazz mentioned this issue May 22, 2016
7 of 7 tasks complete
@thejmazz thejmazz added this to the Week 1 milestone May 22, 2016
@thejmazz
Copy link
Member Author

@thejmazz thejmazz commented May 23, 2016

All papers read and highlighted

@thejmazz
Copy link
Member Author

@thejmazz thejmazz commented May 23, 2016

@thejmazz
Copy link
Member Author

@thejmazz thejmazz commented May 25, 2016

Going to mark this as complete for now. More notes will get done as I write up a blog post on the topic

Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment
Projects
Linked pull requests

Successfully merging a pull request may close this issue.

None yet
2 participants