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jhoogenboom authored
* 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.)
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