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