Hi,
I've two alignment of short reads in bam format. In one sample I've a lot of alignment in one position of the sequence ( ~ 100000 reads aligned ) and in the other sample I've, in the same position, very few aligned reads ( ~ 100 ).
When I load the two bam files in IGV, I wanted to compare (visually) the two alignment. The problem is that the y axis scale is different for the two track and it seems that the two samples have the same number of aligned reads.
Here's a picture

Uploaded with ImageShack.us
How can I have the same scale for the two coverage ?
Thanks
N.
I've two alignment of short reads in bam format. In one sample I've a lot of alignment in one position of the sequence ( ~ 100000 reads aligned ) and in the other sample I've, in the same position, very few aligned reads ( ~ 100 ).
When I load the two bam files in IGV, I wanted to compare (visually) the two alignment. The problem is that the y axis scale is different for the two track and it seems that the two samples have the same number of aligned reads.
Here's a picture

Uploaded with ImageShack.us
How can I have the same scale for the two coverage ?
Thanks
N.
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