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I am trying to trim pacbio sequencing data in a fastq file using trim galore. However, in every run trim galore gets stuck on the trimming step and never goes to the next step. I can see the trimmed file is created and has a relevant size as well.
When I checked the run status I saw that the trim galore job had been suspended for over a day.
Any help regarding this would be great. Thank you for making a nice tool.
SUMMARISING RUN PARAMETERS
==========================
Input filename: ../SRR16******.fastq
Trimming mode: single-end
Trim Galore version: 0.6.10
Cutadapt version: 4.5
Python version: could not detect
Number of cores used for trimming: 4
Quality Phred score cutoff: 7
Quality encoding type selected: ASCII+33
Using Nextera adapter for trimming (count: 468). Second best hit was smallRNA (count: 329)
Adapter sequence: 'CTGTCTCTTATA' (Nextera Transposase sequence; auto-detected)
Maximum trimming error rate: 0.1 (default)
Minimum required adapter overlap (stringency): 1 bp
Minimum required sequence length before a sequence gets removed: 1000 bp
Running FastQC on the data once trimming has completed
The text was updated successfully, but these errors were encountered:
I am not sure I can be of great help here as I have never tried to trim PacBio reads before. Trim Galore is specifically meant to be a short-read trimmer with a focus on Illumina read data. I am not sure if Cutadapt itself is capable of trimming PacBio reads, but maybe there is software out there that is specifically designed to work with it?
hmm, maybe it does work but it just takes a long time? I would probably first try it out with a small subset to see if it works in principle, and if it does through some more parallel compute power at it (via -j). Just monitor the system performance (e.g via top) to make sure that it is still running....
Hey,
I am trying to trim pacbio sequencing data in a fastq file using trim galore. However, in every run trim galore gets stuck on the trimming step and never goes to the next step. I can see the trimmed file is created and has a relevant size as well.
When I checked the run status I saw that the trim galore job had been suspended for over a day.
Any help regarding this would be great. Thank you for making a nice tool.
Cheers,
Aman
Command :
trim_galore -q 7 --fastqc --length 1000 -j 4 -o trimmed ../SRR16*****.fastq
I am also attaching the report generated.
The text was updated successfully, but these errors were encountered: