Genome/read simulator and debugging toolkit for aligners and variant callers. Long Description (required)
Mitty generates reads from genomes or regions, handles ploidy from VCF genotypes, supports tumor/normal and contamination mixes, adds sequencing errors, creates perfect-aligner BAM truth output, and can simulate VCFs with SNPs and indels for aligner/caller testing. genomics; read simulation; variant calling; aligner debugging; VCF; tumor-normal https://github.com/sbg/Mitty
Step 1: Use the attribute tree to add new attributes or remove pre-selected attributes to describe the simulator.
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Summary of Proposed Changes Step 2: Review list of proposed attribute addition(s) and subtraction(s).
Can't Find the Attribute You Are Looking For? If you would like to propose an attribute that you cannot find in the tree above, or if you would like to add a clarification to one or more attributes for this simulator (e.g. a specific file format for attribute /Output/File Format/Other), please list them in the Additional Comment box of the Submit tab .
Summary of Proposed Changes Current Citations/Applications