Open martinezvbs opened 3 months ago
Hi,
I am currently running
nextflow run matsengrp/phip-flow -r main \ --sample_table sample_table.csv \ --peptide_table peptide_table.csv \ --read_length 189 \ --oligo_tile_length 189 \ --output_tall_csv true \ --output_wide_csv true \ --results "$(date -I)" \ -profile docker
and I am getting the following error
executor > local (29) [01/9a1585] process > ALIGN:validate_sample_table (1) [100%] 1 of 1 ✔ [5d/c9e72c] process > ALIGN:validate_peptide_table (1) [100%] 1 of 1 ✔ [c7/a14c72] process > ALIGN:generate_fasta_reference (1) [100%] 1 of 1 ✔ [9b/051e5f] process > ALIGN:generate_index (1) [100%] 1 of 1 ✔ [df/5f63eb] process > ALIGN:short_read_alignment (12) [ 12%] 1 of 8, failed: 1 set -euo pipefail STREAM_FILE_CMD=zcat FASTQ=D152-YO-PCD-BREAST_S16_L001_R1_001.fastq INDEX=peptide_index/peptide ALIGN_OUT_FN=9.sam READ_LENGTH=189 PEPTIDE_LENGTH=117 CPUS=1 MM=2 OP_ARGS="--tryhard --nomaqround --norc --best --sam --quiet" if [ ${PEPTIDE_LENGTH} -lt ${READ_LENGTH} ]; then let TRIM3=${READ_LENGTH}-${PEPTIDE_LENGTH} else TRIM3=0 fi echo $OP_ARGS $STREAM_FILE_CMD $FASTQ | bowtie \ --trim3 $TRIM3 \ --threads $CPUS \ -n $MM \ -l $PEPTIDE_LENGTH \ $OP_ARGS \ -x $INDEX - > $ALIGN_OUT_FN Command exit status: 1 Command error: --tryhard --nomaqround --norc --best --sam --quiet gzip: D152-YO-PCD-BREAST_S16_L001_R1_001.fastq.gz: No such file or directory Error: reads file does not look like a FASTQ file Command: /bowtie-1.3.1-linux-x86_64/bowtie-align-s --wrapper basic-0 --trim3 72 --threads 1 -n 2 -l 117 --tryhard --nomaqround --norc --best --sam --quiet -x peptide_index/peptide -
What could I change to make it work? Thanks!
Hi,
I am currently running
and I am getting the following error
What could I change to make it work? Thanks!