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SOPHiA GENETICS EN
SOPHiA DDM™
SOPHiA DDM™ – How to interprete results/Bioinformatics explanations
SOPHiA DDM™ – How to interprete results/Bioinformatics explanations
Why does the Coverage Calculator in the SOPHiA DDM™ Platform show zero coverage for some genes when other sources indicate there are sufficient reads to detect variants?
What are the criteria for a variant to be classified as a “low confidence” variant?
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