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Would you knowingly leave any stone unturned in your quest to solve an elusive diagnostic odyssey case? Our solution for hereditary disease research is widely adopted, with unsurpassed comprehensiveness of validated content and accuracy. Easily analyze, discover, and interpret the causal agents of the disease for higher case solve rates and peace of mind for more families.
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Do you want to discover the most promising causal variants without spending a lot of time and effort ruling out false positives? Maximize your chance of success with our streamlined solution for analysis to interpretation, and see how it delivers unsurpassed accuracy and coverage for the detection of challenging low frequency variants.
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