Question: Sam Tools Pileup
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gravatar for Patrick Kenneth Gonzales
6.7 years ago by
Can we use the SAM tools pileup tool in Galaxy to get an accurate count of the coverage across the genome? I ask because I have run the pileup tool in Galaxy with bam files generated from tophat and noticed that the coverage reported in the pileup data was consistently lower then what I see in IGV. For example, I look at chr_1, coordinate 3515 and I see 10 reads mapped to that coordinate. I look in the pileup and it reads 1x coverage. I have not applied any filter to the pileup because all I want is a readout of the coverage at each NT including the number of variants that occur. My settings for generate pileup were: do not print mapping quality, print all lines, cap mapping quality to- 0, call consensus according to MAQ model- NO. Any suggestions? Is there a tool in Galaxy other than pileup that can do this? Thanks, Patrick
galaxy • 1.1k views
ADD COMMENTlink written 6.7 years ago by Patrick Kenneth Gonzales20
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