Difference between revisions of "1. Read Quality Assessment"
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Running FASTQC on the raw reads: | Running FASTQC on the raw reads: | ||
+ | |||
+ | Use the following sge script: | ||
#$ -S /bin/sh | #$ -S /bin/sh | ||
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##$ -q amd.q,large.q,intel.q | ##$ -q amd.q,large.q,intel.q | ||
##$ -l h_vmem=40G | ##$ -l h_vmem=40G | ||
− | |||
module load fastqc/0.11.2 | module load fastqc/0.11.2 | ||
− | |||
FILES=/ibers/ernie/scratch/userName/Fastq_RAW/*_4.fq.gz | FILES=/ibers/ernie/scratch/userName/Fastq_RAW/*_4.fq.gz | ||
− | |||
for f in $FILES | for f in $FILES | ||
do | do |
Revision as of 14:10, 6 March 2017
Running FASTQC on the raw reads:
Use the following sge script:
#$ -S /bin/sh #$ -cwd ##$ -q amd.q,large.q,intel.q ##$ -l h_vmem=40G module load fastqc/0.11.2 FILES=/ibers/ernie/scratch/userName/Fastq_RAW/*_4.fq.gz for f in $FILES do fastqc $f done
This generates an html file for each library containing views into the quality of the reads. You can view the results in your favourite web browser.