Hello Jianguang,
Given this information, you will not need to run FASTQ Groomer, but
simply proceed with Fastqc and FASTQ Trimmer.
Best,
Jen
Galaxy team
On 8/14/12 11:12 AM, Du, Jianguang wrote:
Dear All,
I have some FASTQ datasets in phred 33 offset, and I have already
assinged them Fastqsanger format. Do I need to run FASTQ Groomer on
these datasets before I check the data quality by "Fastqc: Fastqc QC"
and "FASTQ Trimmer by column" to remove bad nucleotides at 3' end of reads?
Should I select "Sanger" as "Input FASTQ quality scores type:" if I need
to run Groomer?
Thanks.
Jianguang Du
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