Hi All,
Can you the experienced comment the use of MiSeq in doing RNA-Seq? Is the number of reads with MiSeq too little for RNA-Seq, esp for a big genome such as human? And, do people usually do Paired-end or single-end for RNA-Seq?
Thanks much,
Wingtec
Can you the experienced comment the use of MiSeq in doing RNA-Seq? Is the number of reads with MiSeq too little for RNA-Seq, esp for a big genome such as human? And, do people usually do Paired-end or single-end for RNA-Seq?
Thanks much,
Wingtec
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