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Update README.md to include workaround for processing gVCFs.
Change-Id: I0985dffc7f83b4c4076063521ec1ba983a4b817d
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README.md

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@@ -134,3 +134,7 @@ unambiguous mapping. The guarantee GenomeWarp provides is that all
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confidently-called regions in the target assembly faithfully reproduce the same
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haplotypes as were provided in the query assembly (i.e., GenomeWarp gives 100%
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specificity at a possible sacrifice to sensitivity).
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GenomeWarp currently handles variant-only VCF files (i.e. gVCFs are not
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supported). A gVCF can be processed using the workaround [described
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here](https://github.com/verilylifesciences/genomewarp/issues/2).

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