Wdlupdate (#12)

* removed wording for use on exomes
gatk-workflows · Aug 1, 2018 · 89f11be · 89f11be
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diff --git a/README.md b/README.md
@@ -3,9 +3,7 @@ Workflows used for germline short variant discovery in WGS data
 ### germline_single_sample_workflow :
 This WDL pipeline implements data pre-processing and initial variant calling (GVCF
 generation) according to the GATK Best Practices (June 2016) for germline SNP and
-Indel discovery in human whole-genome sequencing and exome sequencing data. The provided
-intervals in the json are intended for whole-genome sequencing, users are expected to use
-thier own exome intervals for exome sequencing. 
+Indel discovery in human whole-genome sequencing data.
 
 Note: For those users interested in running this wdl on FireCloud (FC), the FC
 version has been provided as fc_germline_single_sample_workflow.wdl. Please visit the 

diff --git a/fc_germline_single_sample_workflow.wdl b/fc_germline_single_sample_workflow.wdl
@@ -2,7 +2,7 @@
 ##
 ## This WDL pipeline implements data pre-processing and initial variant calling (GVCF
 ## generation) according to the GATK Best Practices (June 2016) for germline SNP and
-## Indel discovery in human whole-genome and exome sequencing data.
+## Indel discovery in human whole-genome.
 ##
 ## Requirements/expectations :
 ## - Human whole-genome pair-end sequencing data in unmapped BAM (uBAM) format

diff --git a/germline_single_sample_workflow.wdl b/germline_single_sample_workflow.wdl
@@ -2,7 +2,7 @@
 ##
 ## This WDL pipeline implements data pre-processing and initial variant calling (GVCF
 ## generation) according to the GATK Best Practices (June 2016) for germline SNP and
-## Indel discovery in human whole-genome and exome sequencing data.
+## Indel discovery in human whole-genome.
 ##
 ## Requirements/expectations :
 ## - Human whole-genome pair-end sequencing data in unmapped BAM (uBAM) format