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arq5x committed Apr 8, 2015
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0.14.0 (Future)
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1. Leverage genotype likelihoods in tools (e.g., de_novo and mendelelian_violations (future)) as a means to priortize confident variants.
1. Leverage genotype likelihoods in tools (e.g., de_novo and mendelelian_violations) as a means to prioritize confident variants.
2. Standardize the output from the built-in tools into a common, BED+ format.
3. Update parsing for newer snpEff version
4. Improve and tighten up the database loading.
5. include preprocess script to support varscan, platypus (https://gist.github.com/brentp/4db670df147cbd5a2b32)
5. Include preprocess script to support varscan, platypus (https://gist.github.com/brentp/4db670df147cbd5a2b32)

0.13.0 (2015-Apr-08)
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