Hello Friends,
I am very new to NGS even though I am studying Bioinformatics.
While trying to gain hands on experience on NGS analysis, I have been using tophat on paired end data. I used the following command and my mentor said that my -r option was wrong and asked me to figure it out. The code ran smoothly and I even got the output. But, wat was my mistake is a major concern now.
So, any help is appreciated.
tophat -r 140 -p 4 -o /path/output/ --solexa1.3-quals --library-type fr-unstranded /path/to/ebwt_files /path/to/s_7_1.fq /path/to/s_7_2.fq
I am very new to NGS even though I am studying Bioinformatics.
While trying to gain hands on experience on NGS analysis, I have been using tophat on paired end data. I used the following command and my mentor said that my -r option was wrong and asked me to figure it out. The code ran smoothly and I even got the output. But, wat was my mistake is a major concern now.
So, any help is appreciated.
tophat -r 140 -p 4 -o /path/output/ --solexa1.3-quals --library-type fr-unstranded /path/to/ebwt_files /path/to/s_7_1.fq /path/to/s_7_2.fq
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