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How To Calculate Read Count For Antisense Study?

Hi All, I am going to identify antisense for RNAseq using the R package NASTI-seq, but to run this package we should calculate read counts. Does any one know how to do that.

read

Do you need to perform the read counts in R? If not, you can easily count the number of reads in a FASTQ file by typing, in bash wc -l [your unzipped FASTQ file] and dividing the result by four. If the file is gzipped, then just type zcat [your gzipped FASTQ file] | wc -l

Hi Deedee,

I know how to count read in fastq file. My question is how to calculate them to identifying antisense from mapped data

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