Question: Software for Quality Check of reads
gravatar for utkarsh.sood
2.0 years ago by
utkarsh.sood30 wrote:


I have reads generated for metagenome sequence using Illumina Miseq paired-end reads with the read length of 250 bp. I want to perform the quality check for the obtained sequence.

Could anyone please let me know the software that can be used? I read about Prinseq standalone version but it has various options. I am a little confused about which parameters to use.

I want to remove sequences that have Phred score below 20.


ADD COMMENTlink modified 2.0 years ago by genomax83k • written 2.0 years ago by utkarsh.sood30
gravatar for genomax
2.0 years ago by
United States
genomax83k wrote:

FastQC for general QC. from BBMap for scanning and trimming of data. Some quality related options.

trimq=6             Regions with average quality BELOW this will be trimmed,
                    if qtrim is set to something other than f.  Can be a 
                    floating-point number like 7.3.
maxlength=          Reads longer than this after trimming will be discarded.
                    Pairs will be discarded only if both are longer.
minavgquality=0     (maq) Reads with average quality (after trimming) below 
                    this will be discarded.
maqb=0              If positive, calculate maq from this many initial bases.
minbasequality=0    (mbq) Reads with any base below this quality (after 
                    trimming) will be discarded.
ADD COMMENTlink modified 2.0 years ago • written 2.0 years ago by genomax83k
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