Hi everyone!
Running the fastx-toolkit for my HiSeq data--using the standard protocol I have been in the past for previous data.
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5 results in 0.0021 seconds.
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fastx-toolkit Abort trap: 6 error
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fastq_quality_trimmer
Hi there,
I am confused about the behaviour of fastq_quality_trimmer from the fastx-toolkit.
I use it like so
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counting the details of a .SFF file
Hii All,
Is there a way/utility to get the details of any .SFF file?? I want to
calculate the total no of reads, bases, and Q20... -
Trim the paired-end data
I am a beginner at bioinformatics, please forgive me if I asked silly questions.
I am trying to do the alignment for some paired-end Illumina... -
matching up paired-end reads after fastx-toolkit filtering
Hi,
I just learned that most genome assemblers rely on the order of sequences within paired read files to maintain read pairings. Unfortunately,...
