Changes compared to previous release:

• Change model for HET variants. The model now also considers the distribution of the reads between the reference allele and the variant allele to make overall more accurate predictions.
• Add parameter -q to control the assumed probability of drawing a deletion allele in a HET scenario.
• Add paramter -f to controll the size of the pseudo counts.
• Add paramter -mrg to popdel profile to merge all read groups of one sample.
• Fix wrong type of SVLEN INFO field in VCF header.