Thanks, it works well. The empty reads are removed.
But the head @ characters of the read name line (line1) at each read were also removed.
So I couldn't FastQC these processed fastq...
Hello,
I would like to remove empty reads from fastq_file after trimming adapter sequencing. This fastq is from 454 GS-FLX.
I tried to remove that using following fastx_clipper(in fastx_toolkit)
fastx_clipper -Q33 -l 1 -i in.fastq -o out.fastq
But I received following error message:
Segmentation fault (core dumped)
Anybody has solution about this problem? Other software can remove these empty reads?
Thanks.
If you just want to get rid of short sequences, you can use biowak
bioawk -cfastx 'length($seq) > 1 {print "@"$name"\n"$seq"\n+\n"$qual}'
Edit: FIXED based on comment below!
Thanks, it works well. The empty reads are removed.
But the head @ characters of the read name line (line1) at each read were also removed.
So I couldn't FastQC these processed fastq...
Oh yeah, I forgot. The command should include printing @ before the name:
bioawk -cfastx 'length($seq) > 1 {print "@"$name"\n"$seq"\n+\n"$qual}'
Hello,
I too want to remove the empty reads after the adapter trimming. Could you please elaborate your code
bioawk -cfastx 'length($seq) > 1 {print "@"$name"\n"$seq"\n+\n"$qual}'
I mean what part does what and where is the input file ?
Hey,
bioawk works like a typical awk command but has been modified to understand some of the common ngs file formats (fasta, fastq, gff etc), hence we the -c flag (to consider the format as fastq). Like awk, it needs
awk 'condition{action}' filename.
The condition here is length($seq) > 1 which means length of the sequence is greater than 1
The action here is {print "@"$name"\n"$seq"\n+\n"$qual}' which is to print the sequence back in fastq format (if the condition is satisfied).
You supply the filename after you close the single quote as shown above.
PS: you should not ask a question in a existing thread. This should have been simply a followup comment in the above answer.
Thank you so much Arnstrm.
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In the latest documentation, I can't find a Q flag for the fastx_clipper command. Maybe try removing that flag?