Variant Annotation, Segregation and Exclusion for family or cohort based rare-disease sequencing studies.
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Updated
Jun 2, 2022 - Python
Variant Annotation, Segregation and Exclusion for family or cohort based rare-disease sequencing studies.
Extends core Tripal with support focused on genotypic data, genetic markers, sequence variants, etc.
Code and raw data used in the analyses for: Trans-acting genetic variation affects the expression of adjacent genes via horizontal mechanisms.
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