Hello,
I have mRNASeq data displaying counts per splice variants of mRNA, and I was just wondering how it is possible that the total number of counts in the sample is much higher than the total number of mapped reads (and of total number of reads generated by Illumina).
thank you in advance for your answer,
anna
I have mRNASeq data displaying counts per splice variants of mRNA, and I was just wondering how it is possible that the total number of counts in the sample is much higher than the total number of mapped reads (and of total number of reads generated by Illumina).
thank you in advance for your answer,
anna
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