mrFAST
mrFAST & mrsFAST are designed to map short reads generated with the Illumina platform to reference genome assemblies; in a fast and memory-efficient manner.
Currently Supported Features:
- Output in SAM format
- Indels up to 8 bp (4 bp deletions and 4 bp insertions)
- Paired-end mapping
- Discordant option to generate mapping file ready for VariationHunter to detect structural variants.
- One end anchored (OEA) map locations for novel sequence insertion detection with NovelSeq
- Matepair library mapping (long inserts with RF orientation).
Planned Features: