Entering edit mode
11.2 years ago
rob234king
▴
610
Is there a tool or maybe a method in R to produce a line graph of the coverage of mapped resequencing, for each chromosome of the mapped bam file? I'm looking to compare the coverage across the genome of mapped reads using two different mapping software.
one-line command rocks !
I use your command from above (shown below) but remove some of the spaces in -d ' ' part to get it to work but I don't think my output looks correct? Seems to give me the total reads mapped for each chromosome (note chromosome 0 are a series of contigs which may explain why repeats it) but I'm thinking now that it would be more useful if I could do something more detailed like average coverage every 100 bases and print figure and average position so I could evaluate the coverage between the two mappers over different regions. Couldn't see an option in samtools to refine this command, any suggestions would be welcomed.
Below is the output I'm getting
Thanks