When I used the gene list from RefSeq and ran the DepthofCoverage on a test bam file, I got the output as follows. I wonder why the same gene names are getting repeated (referring to multiple transcripts?). Is there any detailed documentation is available to know how the coverage is getting calculated?. It would be really helpful to understand this better. Gene,total_coverage,average_coverage,Sample_total_cvg,Sample_mean_cvg,Sample_granular_Q1,Sample_granular_median,Sample_granular_Q3,Sample
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