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Is it possible to provide documentation/overview of "logic to skip variant sites that are very clearly germline based on the evidence present in the Normal sample compared to the Tumor sample. This is done at an early stage to avoid spending computational resources on germline events"? Thanks! #11

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kiranchari opened this issue Dec 27, 2017 · 0 comments
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Is it possible to provide documentation/overview of "logic to skip variant sites that are very clearly germline based on the evidence present in the Normal sample compared to the Tumor sample. This is done at an early stage to avoid spending computational resources on germline events"? Thanks! #11

kiranchari opened this issue Dec 27, 2017 · 0 comments

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