Thank you Sean for your answer. So for the first step, should I just extract the aligned bam file from bowtie alignment?
• 0 views
•
link
I have a fastq file and a fasta file with one sequence. I want to plot a figure to show all the reads in fastq file aligned to the fasta file as shown in the figure below. I want to plot for both plus and minus strands. How can I do this (preferably using R)? Thank you for your help. Plot I want: https://ibb.co/eV7EDx
Just a suggestion:
Log in to answer this question.
qualimap(http://qualimap.bioinfo.cipf.es/ ) can be an option once you have the BAM file.