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10.1 years ago
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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!
Are there any examples of command lines to show how to achieve it?
It's something like
but do check the details of the syntax on their website, it changed recently so the above might not be correct (but correct-ish).
What would be the metrics.txt file look like?