From 0845fabbfbf9c5435b65b12cdbc31f27d55cc411 Mon Sep 17 00:00:00 2001 From: Florent Yvon Date: Mon, 11 Mar 2024 15:02:13 +0000 Subject: [PATCH] Fixed typo --- curation/scripts/qc_ref_genome_readme.md | 4 ++-- 1 file changed, 2 insertions(+), 2 deletions(-) diff --git a/curation/scripts/qc_ref_genome_readme.md b/curation/scripts/qc_ref_genome_readme.md index bffd06b5..6a52b557 100644 --- a/curation/scripts/qc_ref_genome_readme.md +++ b/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. \ No newline at end of file +* *flip*: default is off. If flip is on, all variants will be tested against the reverse strand if using coordinates without rsID.