feat: improve coverage stratification for datasets with high coverage #75
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Previous coverage stratification was only 1-10, 10-30 and >= 30. Whole exome sequencing datasets used for benchmarking somatic variant calling include much higher coverages. Therefore the coverage stratification for those datasets is expanded with categories 30-50 (instead of >=30), 50-100, 100-300 and >=300.
Currently coverage stratification is chosen via parameter in preset.yaml for each benchmark. This does not work with the expand statement in rule eval in the Snakefile.