[ENH] add autosomal dominant tool
[ENH] upgrade to dbSNP build 137
[ENH] upgrade to ESP 6500 samples (from 5400)
[ENH] added new de_novo mutations tool.
[DOC] Minor tweaks
[ENH] store the depth of aligned sequence for each sample.  The _genotype_'s DP column.
omitted from previous commit
[ENH] Add new tool (gemini de_novo) for finding cand. de novo mutations in trios.
track gemini_subjects.py and update auto_* tools
[ENH] update 1000G VCF annotation file
[ENH] added first cut at testing suite
several tweaks to gemini_query.py
prefer HET, HOM_REF, HOM_ALT, UNKNOWN for genotype constants
tweaks to is_exonic and is_coding
add OrderedSet to utilities
tweaks to snpEff exonic logic
minor tweaks to test suite
[DOC] Add genotype-specific query examples to README
typo
Update README.md

Readme typos.