29 Feb
2012
29 Feb
'12
9:39 a.m.
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