16  Variant calling analysis

16.1 Common mutations

16.2 Structural variants

16.3 Genome rearrangements

16.4 Read mapping algorithms and programs

16.4.1 Burrow-Wheeler-Alignment

16.4.2 BWA-MEM2

16.4.3 Minimap2

16.4.4 SAM, BAM and CRAM formats

16.5 Identifying mutations

16.5.1 Freebayes and Snippy

16.5.2 The VCF file