You can avoid the space/time overhead of grooming and get
comprehensive QC reports using the new wrapper for FastQC (under NGS:
QC) - it takes fastq of any flavour (and bam) groomed or not,
producing a superset of the compute quality stats output without the
need for an intermediate step. Highly recommended.

On Wed, Jun 1, 2011 at 12:02 PM, John David Osborne <ozb...@uab.edu> wrote:
> I noticed that for our new Ilumina data (which generate Sanger format) the
> FastQ groomer output is identical to the Ilumina FastQ input file.
>
> I was hoping to go ahead and just use the raw FastQ files as input (saving
> disk space) for computing quality statistics to look at box plots, but it
> appears that the tool "Compute Quality Statistics" appears to require that
> the data have been run through FastQ Groomer first.
>
> Is there a way to get around this and is this a bug? I assuming this is some
> sort of safety measure built into this tool?
>
>  -John
>
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-- 
Ross Lazarus MBBS MPH;
Associate Professor, Harvard Medical School;
Director of Bioinformatics, Channing Lab; Tel: +1 617 505 4850;
Head, Medical Bioinformatics, BakerIDI; Tel: +61 385321444;

___________________________________________________________
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