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We need cram output to run with the Sanger pipeline.
trim off the first 5 bases of those libs. This is recommended by arima and they suggest to use a simple awk-script to do that:
zcat INPUT.fastq.gz | awk '{ if(NR%2==0) {print substr($1,6)} else {print} }' | gzip > OUTPUT.fastq.gz
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We need cram output to run with the Sanger pipeline.
The text was updated successfully, but these errors were encountered: