In order for SeqMan Pro to display the MID column in the Variant Report, you must choose either the diploid Bayesian or haploid Bayesian method of variant calculation prior to assembly in SeqMan NGen. This can be done from the following dialogs:
•Assembly Options dialog > Advanced Assembly Options button > Variants tab > SNP calculation method drop-down menu = Diploid Bayesian or Haploid Bayesian.
•Recalculate Variants > Variant Options button > SNP calculation method drop-down menu = Diploid Bayesian or Haploid Bayesian.
If you instead choose the “simple percentage” method for variant calculation from the drop-down menu, the MID column will be omitted from the Variant Report.