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, 

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