Thanks for helping Felix. A simple typo on my end unfortunately. Problem solved!
Unconfigured Ad
Collapse
X
-
For those with weaker heart (those that cannot use complex scripts in Linux and need a graphic interface)
here is another (free) program for trimming qualities:
An efficient SFF/FastQ viewer and editor (GUI)

The gray/green curves in the second graphic shows the average quality before and after trimming the low quality ends.
Only works on Fasta, FastQ, SFF for the moment.
Sorry.Last edited by create.share; 05-30-2015, 12:19 AM.
Comment
-
Hi everyone,
not sure if this is the right thread but I'll give it a go:
I'm trying to get rid of adapters in my sequences. There aren't many with adapters but I'd like to save what I can.
When I run my command I get the following error:
==================================================================
Your job looked like:
------------------------------------------------------------
# LSBATCH: User input
/gpfs/scratch/cbh12wsu/trim/trim_galore -phred33 --illumina --paired -phred33 --path_to_cutadapt /gpfs/scratch/cbh12wsu/trim/cutadapt.py -o adaptrim.fastq -length 50 1_L.fastq 2_R.fastq
------------------------------------------------------------
Exited with exit code 2.
The output (if any) follows:
Path to Cutadapt set as: '/gpfs/scratch/cbh12wsu/trim/cutadapt.py' (user defined)
File "/gpfs/scratch/cbh12wsu/trim/cutadapt.py", line 99
print(rest, match.read.name, file=self.file)
^
SyntaxError: invalid syntax
Cutadapt seems to be working fine (tested command '/gpfs/scratch/cbh12wsu/trim/cutadapt.py --version')
File "/gpfs/scratch/cbh12wsu/trim/cutadapt.py", line 99
print(rest, match.read.name, file=self.file)
^
SyntaxError: invalid syntax
Failed to write to file '1_L.fastq_trimming_report.txt': No such file or directory
==================================================================
Does indicate a problem with the cutadapt.py?
Thanks!
Comment
-
Hmm, when you just type "/gpfs/scratch/cbh12wsu/trim/cutadapt.py" on the command line do you see something like:
?Code:cutadapt version 1.8.1 Copyright (C) 2010-2015 Marcel Martin <[email protected]> cutadapt removes adapter sequences from high-throughput sequencing reads. Usage: cutadapt -a ADAPTER [options] [-o output.fastq] input.fastq
Comment
-
Hi Felix,
thanks for replying so quick!
I get the following error when I try your command:
File "/gpfs/scratch/cbh12wsu/trim/cutadapt.py", line 99
print(rest, match.read.name, file=self.file)
^
SyntaxError: invalid syntax
I think I should mention that I made cutadapt.py an executable. And copied it from it's original folder into the trim folder.
Comment
-
I put it back where it belongs and tried again. Same error as before.
With normal installation you mean the pip command? I tried that before but I'm not allowed to do that on the cluster. I can load a cutadapt module but I was hoping making it an executable would solve the problem.
Comment
-
I've installed it and when I run felix's command I get:
cutadapt version 1.8.1
...
But I still get this error:
Path to Cutadapt set as: '/gpfs/scratch/cbh12wsu/trim/cutadapt/cutadapt/scripts/cutadapt' (user defined)
1.8.1
Cutadapt seems to be working fine (tested command '/gpfs/scratch/cbh12wsu/trim/cutadapt/cutadapt/scripts/cutadapt --version')
Failed to write to file '1_L.fastq_trimming_report.txt': No such file or directory
Used this command:
bsub -N -q short -o cut3.txt "/gpfs/scratch/cbh12wsu/trim/trim_galore -phred33 --illumina --paired -phred33 --path_to_cutadapt /gpfs/scratch/cbh12wsu/trim/cutadapt/cutadapt/scripts/cutadapt -o adaptrim.fastq -length 50 1_L.fastq 2_R.fastq"
More ideas?
Comment
-
no that shouldn't matter... Could it be that your queuing system does not take you to the same directory (option like -cwd)? What happens if you just run the command without using the queue?
By the way you can shorten the command like this:
By the way -o is meant to be an output directory, not a file name. This might be the reason why it can't create the output files in the directory called adaptrim.fastqCode:/gpfs/scratch/cbh12wsu/trim/trim_galore --paired --path_to_cutadapt /gpfs/scratch/cbh12wsu/trim/cutadapt/cutadapt/scripts/cutadapt [COLOR="Red"]-o adaptrim.fastq[/COLOR] -length 50 1_L.fastq 2_R.fastq
Comment
Latest Articles
Collapse
-
by SEQadmin2
NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...-
Channel: Articles
Today, 06:46 AM -
-
by SEQadmin2
Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?
Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating...-
Channel: Articles
10-14-2026, 09:55 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Genome Sequencing Reveals Large, Repeat-Rich DNA in Trapdoor Spider Named for Stephen Colbert
by SEQadmin2
Started by SEQadmin2, 10-28-2026, 09:57 AM
|
0 responses
22 views
0 reactions
|
Last Post
by SEQadmin2
10-28-2026, 09:57 AM
|
||
|
Started by SEQadmin2, 10-28-2026, 09:51 AM
|
0 responses
14 views
0 reactions
|
Last Post
by SEQadmin2
10-28-2026, 09:51 AM
|
||
|
Started by SEQadmin2, 10-22-2026, 11:13 AM
|
0 responses
67 views
0 reactions
|
Last Post
by SEQadmin2
10-22-2026, 11:13 AM
|
||
|
Started by SEQadmin2, 10-22-2026, 10:48 AM
|
0 responses
47 views
0 reactions
|
Last Post
by SEQadmin2
10-22-2026, 10:48 AM
|
Comment