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2 changes: 1 addition & 1 deletion src/sites/iva/conf/opencga-variant-constants.js
Original file line number Diff line number Diff line change
Expand Up @@ -868,7 +868,7 @@ const tooltips = {
"This knowledge is both human-readable and machine-readable, and is a foundation for computational analysis of large-scale molecular biology and genetics experiments in biomedical research.",
hpo: "The Human Phenotype Ontology (HPO) provides a standardized vocabulary of phenotypic abnormalities encountered in human disease.",
clinvar: "Filter out variants falling outside the genomic features (gene, transcript, SNP, etc.) defined",
fullTextSearch: "Filter out variants falling outside the genomic features (gene, transcript, SNP, etc.) defined",
fullTextSearch: "Filter out variants that do not match with the IDs or the full text provided",
cadd: "Raw values have relative meaning, with higher values indicating that a variant is more likely to be " +
"simulated (or not observed) and therefore more likely to have deleterious effects. If discovering causal variants " +
"within an individual, or small groups, of exomes or genomes te use of the scaled CADD score is recommended",
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