Identification of cancer-causing variants
bioinformatics
annotations
clinical
dbsnp
variants
cancer-genomics
clinvar
diseases
cancer-research
grch37
cancer-detection
allele-frequencies
conservation-scores
functional-prediction
pathogenic-variants
dbnsfp
gnomad
clinical-significance
hereditary-cancer-syndrome
acmg-guidelines
-
Updated
Apr 19, 2024 - Python