Dear Glaxy users and admin
I ran my sequence data on FASTQC tool,
output says it is
EncodingSanger / Illumina 1.9
now i want to groom my file, but groomer does not have option for 1.9 in "Input
FASTQ quality scores type"
any idea which option i should select to grroom my file,
later i want to run Bowtie or Tophat,
Thanks
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