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Update README since gVCF inputs are now supported
Change-Id: I583dc2d07b4359c82d315dd353973789237ab889
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README.md

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@@ -134,7 +134,3 @@ 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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