TP métagénomique

16S_workflow.sh 1.1KB

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  1. #!/bin/bash
  2. raw_reads_dir=$1
  3. output_dir=$2
  4. #mkdir $output_dir
  5. #mkdir trimmed_reads
  6. #TRIM READS WITH ALIENTRIMMER
  7. #for R1 in $(ls $raw_reads_dir/*R1.fastq);
  8. # do
  9. # R2=`echo $R1 | sed 's/R1/R2/g'`
  10. # oR1=`echo $R1 | sed 's/\.fastq/\.at\.fq/g'`
  11. # oR1=`echo $oR1 | sed 's/fastq\///g'`
  12. # oR2=`echo $R2 | sed 's/\.fastq/\.at\.fq/g'`
  13. # oR2=`echo $oR2 | sed 's/fastq\///g'`
  14. # java -jar soft/AlienTrimmer.jar -if $R1 -ir $R2 -q 20 -c databases/contaminants.fasta -of trimmed_reads/$oR1 -or trimmed_reads/$oR2
  15. # done
  16. # MERGE READS AND OUTPUT FASTA
  17. mkdir fasta
  18. for R1 in $(ls trimmed_reads/*R1.at.fq);
  19. do
  20. R2=`echo $R1 | sed 's/R1/R2/g'`
  21. outname=`echo $R1 | sed 's/_R1\.at\.fq/\.fasta/g'`
  22. label=`echo $outname | sed 's/trimmed_reads\///g'`
  23. outname=`echo $outname | sed 's/trimmed_reads/fasta/g'`
  24. label=`echo $label | sed 's/\.fasta//g'`
  25. soft/vsearch --fastq_mergepairs $R1 --reverse $R2 --fastaout $outname --label_suffix ";sample=$label;"
  26. done
  27. # MERGE ALL FASTAS TO 'amplicon.fasta'
  28. cat fasta/*.fasta > fasta/amplicon.fasta