Fixed typo

curation/scripts/qc_ref_genome_readme.md

@@ -1,6 +1,6 @@
 ## About the reference genome QC script
 
-This scripts verifies if the variant positions of a scoring file match the given reference genome.
+This script verifies if the variant positions of a scoring file match the given reference genome.
 
 ### How it works
 
@@ -31,4 +31,4 @@ qc_ref_genome.py [-h] [--scoring_file SCORING_FILE] [--ref {auto,37,38}] [--n_re
 * *scoring_file* : the scoring file to validate (unzipped)
 * *ref*: allowed values: **auto**, **37**, **38**. If set to auto, the reference genome found in the header of the scoring file will be used.
 * *n_requests*: maximum number of requests (or number of samples) sent to the Ensembl API. Default: **1**
-* *flip*: default is off. If flip is on, all variants will be tested against the reverse strand if using coordinates without rsID.
+* *flip*: default is off. If flip is on, all variants will be tested against the reverse strand if using coordinates without rsID.