Dear Glaxy users and admin
I ran my sequence data on FASTQC tool,
output says it is
Encoding
Sanger / 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