--- a/snpEff.xml	Tue Mar 27 14:56:29 2018 -0400
+++ b/snpEff.xml	Thu Mar 29 20:39:49 2018 -0400
@@ -1,4 +1,4 @@
-<tool id="snpEff" name="SnpEff eff:" version="@wrapper_version@.1">
+<tool id="snpEff" name="SnpEff eff:" version="@wrapper_version@.galaxy1">
     <description> annotate variants</description>
     <macros>
         <import>snpEff_macros.xml</import>
@@ -386,7 +386,7 @@
 
 By genetic variant we mean difference between a genome and a "reference" genome. As an example, imagine we are sequencing a "sample". Here "sample" can mean anything that you are interested in studying, from a cell culture, to a mouse or a cancer patient.  It is a standard procedure to compare your sample sequences against the corresponding "reference genome". For instance you may compare the cancer patient genome against the "reference genome".
 
-In a typical sequencing experiment, you will find many places in the genome where your sample differs from the reference genome. These are called "genomic variants" or just "variants". 
+In a typical sequencing experiment, you will find many places in the genome where your sample differs from the reference genome. These are called "genomic variants" or just "variants".
 Typically, variants are categorized as follows:
 
  - SNP (Single-Nucleotide Polymorphism) Reference = 'A', Sample = 'C'
@@ -397,7 +397,7 @@
 
 This is not a comprehensive list, it is just to give you an idea.
 
-Suppose you have a huge file describing all the differences between your sample and the reference genome. But you want to know more about these variants than just their genetic coordinates. E.g.: Are they in a gene? In an exon? Do they change protein coding? Do they cause premature stop codons? SnpEff can help you answer all these questions. The process of adding this information about the variants is called "Annotation". 
+Suppose you have a huge file describing all the differences between your sample and the reference genome. But you want to know more about these variants than just their genetic coordinates. E.g.: Are they in a gene? In an exon? Do they change protein coding? Do they cause premature stop codons? SnpEff can help you answer all these questions. The process of adding this information about the variants is called "Annotation".
 SnpEff provides several degrees of annotations, from simple (e.g. which gene is each variant affecting) to extremely complex annotations (e.g. will this non-coding variant affect the expression of a gene?). It should be noted that the more complex the annotations, the more it relies in computational predictions. Such computational predictions can be incorrect, so results from SnpEff (or any prediction algorithm) cannot be trusted blindly, they must be analyzed and independently validated by corresponding wet-lab experiments.
 
 @snpeff_in_galaxy_info@