I am looking to call my samples that were exome sequenced using UnifiedGenotyper program within GATK. An example of a generic command is given in the following link under “Example generic command for multi-sample SNP calling” and I am assuming that it should work for calling a single sample
I have a question on the –dcov option, what does it mean?
Also, I have seen examples of where they added -A DepthOfCoverage \
-A AlleleBalance \. Is there an optimal parameter setting to call variants for exome sequencing?
Thanks,
I have a question on the –dcov option, what does it mean?
Also, I have seen examples of where they added -A DepthOfCoverage \
-A AlleleBalance \. Is there an optimal parameter setting to call variants for exome sequencing?
Thanks,
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