Hi all,
To do fastq grooming on galaxy, I have to choose fastq input format, either Illumina 1.3-1.7 or Sanger, for reads done on HiSeq 2000 using GAPipeline vRTA1.10.36. A quality sample from the end of a 210 base read:
6;95;6HHHHHHHHHHHHHHHHHHHHHHHHHHFHFFHHFFFHFFHHHFFFH>?AA>#@<?##
If anyone can help me understand which input format to select, much abliged.
To do fastq grooming on galaxy, I have to choose fastq input format, either Illumina 1.3-1.7 or Sanger, for reads done on HiSeq 2000 using GAPipeline vRTA1.10.36. A quality sample from the end of a 210 base read:
6;95;6HHHHHHHHHHHHHHHHHHHHHHHHHHFHFFHHFFFHFFHHHFFFH>?AA>#@<?##
If anyone can help me understand which input format to select, much abliged.
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