Are there any examples of command lines to show how to achieve it?
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Dear colleagues:
I have got whole exome sequencing data of dozens of samples. I want to know how we can get the exome data capture quality index of coverage ratio.
Any help that can help me to understand the question would be appreciated.
Best!
Sounds like a job for Picard CalculateHsMetrics.
Run it on each bam file, then check the column PCT_SELECTED in the output metrics file for each sample.
Are there any examples of command lines to show how to achieve it?
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