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

Comments

2 participants
@thejmazz
Member

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 referenced this issue May 22, 2016

Closed

Week 1 #9

7 of 7 tasks complete

@thejmazz thejmazz added this to the Week 1 milestone May 22, 2016

@thejmazz

This comment has been minimized.

Member

thejmazz commented May 23, 2016

All papers read and highlighted

@thejmazz

This comment has been minimized.

Member

thejmazz commented May 23, 2016

@thejmazz

This comment has been minimized.

Member

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