mkfastq run on high power node, version 2.1.1

CHANGELOG.md

-# v2.1.0
+# v2.1.1
 **UserFacing**
 * Check Design File for spaces in name and file contents
 * Update design example, README, and astrocyte.yml with current barcode IDs

workflow/main.nf

@@ -8,6 +8,14 @@ main.nf
 *
 */
 
+//  ########  ####  ######  ######## 
+//  ##     ##  ##  ##    ## ##       
+//  ##     ##  ##  ##       ##       
+//  ########   ##  ##       ######   
+//  ##     ##  ##  ##       ##       
+//  ##     ##  ##  ##    ## ##       
+//  ########  ####  ######  ##       
+
 // Define input variables
 params.name = "run"
 params.bcl = "${baseDir}/../test_data/simple1/*.tar.gz"
@@ -24,7 +32,7 @@ bclCount = Channel
   .count()
 
 // Define regular variables
-pipelineVersion = "2.1.0"
+pipelineVersion = "2.1.1"
 name = params.name
 designLocation = Channel
   .fromPath(params.designFile)
@@ -142,6 +150,7 @@ process mkfastq {
 
   tag "${bcl.simpleName}"
   publishDir "${outDir}/${task.process}", mode: 'copy', pattern: "{*/outs/**/*.fastq.gz}"
+  queue '128GB,256GB,256GBv1,384GB'
   module 'cellranger/3.1.0:bcl2fastq/2.19.1'
 
   input:

workflow/nextflow.config

@@ -47,6 +47,6 @@ manifest {
   homePage = 'https://git.biohpc.swmed.edu/BICF/Astrocyte/cellranger_mkfastq'
   description = 'This pipeline is a wrapper for the cellranger mkfastq tool from 10x Genomics (which uses Illuminas bcl2fastq). It takes bcls and demultiplexes samples from 10x Genomics Single Cell Gene Expression libraries into fastqs.'
   mainScript = 'main.nf'
-  version = '2.1.0'
+  version = '2.1.1'
   nextflowVersion = '>=0.31.0'
 }