Dear all,
here i have a question "whether the unique mapping reads should be extracted in Small RNA-Seq".
i have some datasets, useing bowtie for mapping the reads, only about 30% of the mapping reads are uniqued mapped. Is this normal? and my species is human.
thanks
here i have a question "whether the unique mapping reads should be extracted in Small RNA-Seq".
i have some datasets, useing bowtie for mapping the reads, only about 30% of the mapping reads are uniqued mapped. Is this normal? and my species is human.
thanks