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1.the raw data is the pair-end illumina GA2 data, but after the transformation
the result contains 3: xxxx_1.fastq,xxxx_2.fastq,xxxx.fastq,and the xxxx.fastq 's size is very small. Is that means xxxx.fastq is the unpaired reads?
2.I use the fastq-dump command, is that suitable to the sequencing value of illumina GA2? or I should try the illumina-dump...
I am a rookie. Thank you all guys in advance
the result contains 3: xxxx_1.fastq,xxxx_2.fastq,xxxx.fastq,and the xxxx.fastq 's size is very small. Is that means xxxx.fastq is the unpaired reads?
2.I use the fastq-dump command, is that suitable to the sequencing value of illumina GA2? or I should try the illumina-dump...
I am a rookie. Thank you all guys in advance
