Entering edit mode
3.9 years ago
hans
▴
20
Hello I need to map Illumina's 150PE RNAseq reads to a reference genome. I wonder if minimap is suitable for this task or I should use different software. The goal of the mapping is variant calling. If minimap is a good choice, which parameters should I use? Thank you
I eventually found the the answer in minimap manual: "Minimap2 does not work well with short spliced reads. There are many capable RNA-seq mappers for short reads."