Random Forest classifier designed to predict pairs of human genes capable to causing a digenic disease when carrying rare variants simultaneously. DiGePred has been trained using digenic pairs from DIDA and non-digenic pairs from unaffected relatives of individuals with rare undiagnosed disease.
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GRCh37, will the package be updated for GRCh38 use? #3
Our in house protocol are all performed under GRCh38
However, DiGePred still use GRCh37, I am wandering there are plans to update?
Or are there any recommendations on how may I approach this issue?
Hello,
Our in house protocol are all performed under GRCh38 However, DiGePred still use GRCh37, I am wandering there are plans to update? Or are there any recommendations on how may I approach this issue?