Dear all,

Initially, I had 4 .fastq file, L001-L004, obtained from NGS of a mixture of RNAs. After several processes, I got 4 corresponding sorted bam files. Now, I want to obtain a text file that show the starting position of reads in reference sequences. However, by using

for i in *.sorted.bam; do bedtools genomecov -d -5 -ibam $i > $i.txt; done

I was only able to obtain 4 seperate txt file. Moreover, starting positions that have no reads were also included. Here is your reference when position 2, 4, 7, 10 were included:

Pri-let-7e 1 3

Pri-let-7e 2 0

Pri-let-7e 3 1

Pri-let-7e 4 0

Pri-let-7e 5 1

Pri-let-7e 6 2

Pri-let-7e 7 0

Pri-let-7e 8 1

Pri-let-7e 9 1

Pri-let-7e 10 0

Pri-let-7e 11 1

Pri-let-7e 12 3

So, is there any way that I can take to get ONE txt file reporting the starting positions with read counts from 4 sorted bam files and obmitting that with 0 count? Thank you all!

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