* Allelefinder can now combine data from multiple files into a
  single sample (this happens when the same sample tag was
  extracted from their names).
* Allelefinder can now automatically convert sequences to a given
  format (this is optional though). This is particularly useful
  when combining the knownalleles.csv and newalleles.csv files of
  a sample. (Note that allelefinder still assumes that the files
  contain different alleles; no attempt is made to check whether
  the same allele was represented in multiple files.)