From be512736683cf29aa50e3c8da2b78443ddb03a8b Mon Sep 17 00:00:00 2001 From: not populated not populated <ameynert@sdf-cs1.eidf.epcc.ed.ac.uk> Date: Wed, 29 Sep 2021 13:41:36 +0100 Subject: [PATCH] Links rather than text copy for config files and bcbio templates --- ...SOP_alignment_variant_annotation_ultra2.md | 48 +------------------ 1 file changed, 2 insertions(+), 46 deletions(-) diff --git a/docs/SOP_alignment_variant_annotation_ultra2.md b/docs/SOP_alignment_variant_annotation_ultra2.md index 4800942..097facb 100644 --- a/docs/SOP_alignment_variant_annotation_ultra2.md +++ b/docs/SOP_alignment_variant_annotation_ultra2.md @@ -78,55 +78,11 @@ The project working directories will be in the folder `/home/u035/u035/shared/an ## Project configuration -A configuration script sets environment variables common to scripts used in this SOP. This is stored at `/home/u035/u035/shared/scripts/trio_whole_exome_config.sh`. - -``` -#!/usr/bin/bash -# -# Basic configuration options for trio WES pipeline -# - -BASE=/home/u035/u035/shared -SCRIPTS=$BASE/scripts -BCBIO_TEMPLATE=$SCRIPTS/trio_whole_exome_bcbio_template.yaml -TARGET=$BASE/resources/Twist_Exome_RefSeq_targets_hg38.plus15bp.bed -DOWNLOAD_DIR=$BASE/data -REFERENCE_GENOME=$BASE/software/bcbio/genomes/Hsapiens/hg38/seq/hg38.fa - -PARAMS_DIR=$BASE/analysis/params -READS_DIR=$BASE/analysis/reads -CONFIG_DIR=$BASE/analysis/config -WORK_DIR=$BASE/analysis/work -OUTPUT_DIR=$BASE/analysis/results - -export PATH=$BASE/software/bcbio/tools/bin:$PATH -```` +A [configuration script](../trio_whole_exome_config.sh) sets environment variables common to scripts used in this SOP. ## Template for bcbio configuration -Bcbio requires a template file in YAML format to define the procedures run in the pipeline. The template for this project is stored at `/home/u035/u035/shared/scripts/trio_whole_exome_bcbio_template.yaml`. - -``` -details: -- algorithm: - platform: illumina - quality_format: standard - aligner: bwa - mark_duplicates: true - realign: false - recalibrate: true - effects: vep - effects_transcripts: all - variantcaller: gatk-haplotype - indelcaller: false - remove_lcr: true - tools_on: - - vep_splicesite_annotations - analysis: variant2 - genome_build: hg38 -upload: - dir: /home/u035/u035/shared/results -``` +Bcbio requires a [template file in YAML format](../trio_whole_exome_bcbio_template.yaml). to define the procedures run in the pipeline. Runs from the Edinburgh CRF have a [slightly different template file](../trio_whole_exome_bcbio_crf_template.yaml) which adds read trimming parameters specific to NextSeq 2000 output. ## Output -- GitLab