custom_scripts_for_16s_rrna_sequence_analysis
Custom scripts for 16S rRNA sequence analysis
merge_paired_fastq.sh
#!/bin/bash # # modified from 'Merge_Reads_Script.sh' available from: # https://github.com/edamame-course/Amplicon_Analysis/blob/master/resources/Merged_Reads_Script.sh # out=merged_dir if [ ! -d merged_reads ]; then echo Creating ${out} directory... mkdir ${out} fi for f in *F_sub.* do if [ ! -e ${f} ]; then echo Can\'t find 'F_sub' reads! echo You have to set fwd/rev read indicators in this script! exit fi r=$(sed -e "s/F_sub/R_sub/" <<< "$f") file=$(cut -d_ -f1 <<< "$f") echo Processing ${f} and ${r} '===>' ${out}/${file}_merged.fastx join_paired_ends.py -f ${f} -r ${r} -o ${file}/ mv ${file}/fastqjoin.join.fastq ${out}/${file}_merged.fastq convert_fastaqual_fastq.py -c fastq_to_fastaqual -f ${out}/${file}_merged.fastq -o ${out}/${file} mv ${out}/${file}/${file}_merged.fna ${out}/${file}_merged.fasta rm -r ${out}/${file} rm -r ${file}/ done
custom_scripts_for_16s_rrna_sequence_analysis.txt · Last modified: 2021/03/17 13:09 by 127.0.0.1