Hi! I'm working with Illumina paired end short reads fastq mapping using Artemis for a course I'm taking. While I'm able to get all SAM/BAM files without errors, I noticed my mapping visualization on Artemis looks different than it should: I understand (From the manual and various online tutorials) that there should be blue (unique reads) and green (dupliate reads) stacks on the BAM panel, but I only get blue ones (even for actual duplicated reads).
Has anyone experienced anything like this?
Has anyone experienced anything like this?