I'm processing two fastq files through the Du Novo pipeline. I planned to proceed as suggested by the processing steps posted in the github page. At the 'optional' error correction step, the program produces an error:
"Could not locate a Bowtie index corresponding to basename "refdir/barcodes-ref".
Command: bowtie-align --wrapper basic-0 --chunkmbs 512 --threads 1 -f --sam -a --best -v 3 refdir/barcodes-ref refdir/barcodes.fa /rugpfs/fs0/marr_lab/store/jmathai/WTminus/Analysis_dunovo/barcodes.sam
I've provided the script details below. If you could clarify why this error is occurring, that would be greatly appreciated!
Thanks!
SCRIPT:
conda activate dunovo
DUNOVO_HOME="/rugpfs/fs0/marr_lab/store/jmathai/softwares/miniconda/envs/dunovo/dunovo"
RAW_DATA="/rugpfs/fs0/marr_lab/store/jmathai/WTminus"
WORKING_DIR="/rugpfs/fs0/marr_lab/store/jmathai/WTminus/Analysis_dunovo"
cd $WORKING_DIR
pwd
## Sort the reads into families based on their barcodes and split the barcodes from the sequence
$DUNOVO_HOME/make-families.sh $RAW_DATA/WTminus_R1.fastq $RAW_DATA/WTminus_R2.fastq > families.tsv
echo "[CMD] make-families.sh $RAW_DATA/WTminus_R1.fastq $RAW_DATA/WTminus_R2.fastq > families.tsv"
## Correct errors in barcodes
$DUNOVO_HOME/baralign.sh families.tsv refdir $WORKING_DIR/barcodes.sam
echo "[CMD] baralign.sh families.tsv refdir barcodes.sam"
$DUNOVO_HOME/correct.py families.tsv refdir/barcodes.fa barcodes.sam | sort > families.corrected.tsv
echo "[CMD] correct.py families.tsv refdir/barcodes.fa barcodes.sam | sort > families.corrected.tsv"
Hi,
I'm processing two fastq files through the Du Novo pipeline. I planned to proceed as suggested by the processing steps posted in the github page. At the 'optional' error correction step, the program produces an error:
I've provided the script details below. If you could clarify why this error is occurring, that would be greatly appreciated!
Thanks!
SCRIPT: