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In most cases, the next step would be to remove duplicate reads and to ensure that base quality scores are properly calibrated. To save time, we'll skip those steps now.
In most cases, the next step would be to remove duplicate reads and to ensure that base quality scores are properly calibrated. To save time, we'll skip those steps now.
=== Calling variants and Inferring genotypes ===
== Initial set of variant calls ==
== Initial set of variant calls ==
