Closed ArtPoon closed 2 years ago
iVar seems to be popular for Illumina data: https://github.com/andersen-lab/ivar
Need to adapt existing pipeline to record not only individual mutations, but also mutations observed in linkage in short reads - this will need some custom data structure
See reading list
How much will we have to modify these existing pipelines to obtain frequency data of individual polymorphisms (substitutions, indels)?