Add one more SCE after initial assignment, if it improves concordance. Add more than one if necessary to render the assignment valid.

Script for improved SCE calling based on comparing single-cell segmentations to multi-cell segmentations

Upgrade environment to get WhatsHap 0.17, which correctly handles haplotagging when chromosomes are missing in VCF file

Add means to narrow down the number of considered genotypes (a bit less drastic than forcing biallelic); apply haplotag probabilities only after that

subset regions to the regions that have non-zero read count

Added rules to re-genotype a set of given SNVs (e.g. from 1000G) and to do haplotagging of BAM files. Slightly reorganized input file structure: now expect two separate folders "bam/{sample}/selected" and "bam/{sample}/all", where "selected" should contain the good Strand-seq libraries, where all should contain all libraries that can be used for SNV calling/genotyping.