From a97e34ad19d8c6e9d33ce2f87ac313ac93335e21 Mon Sep 17 00:00:00 2001
From: Cory McLean <cym@google.com>
Date: Thu, 20 Sep 2018 09:26:51 -0400
Subject: [PATCH] Update README since gVCF inputs are now supported

Change-Id: I583dc2d07b4359c82d315dd353973789237ab889
---
 README.md | 4 ----
 1 file changed, 4 deletions(-)

diff --git a/README.md b/README.md
index faf9e11..971b473 100644
--- a/README.md
+++ b/README.md
@@ -134,7 +134,3 @@ unambiguous mapping. The guarantee GenomeWarp provides is that all
 confidently-called regions in the target assembly faithfully reproduce the same
 haplotypes as were provided in the query assembly (i.e., GenomeWarp gives 100%
 specificity at a possible sacrifice to sensitivity).
-
-GenomeWarp currently handles variant-only VCF files (i.e. gVCFs are not
-supported). A gVCF can be processed using the workaround [described
-here](https://github.com/verilylifesciences/genomewarp/issues/2).