ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants

Keyphrases

• Allele Frequency 100%
• NsSNPs 100%
• Prediction Tool 100%
• Disease Pattern 50%
• Cancer Disease 50%
• Pathogenicity 50%
• Area under the Curve 50%
• Machine Learning Algorithms 50%
• Rare Diseases 50%
• Human Genome 50%
• Training Set 50%
• Cause of Disease 50%
• High-throughput DNA Sequencing 50%
• Loss Function 50%
• Computational Approach 50%
• Two-machine 50%
• Phenotypic Effects 50%
• Exome 50%
• Superior Accuracy 50%
• Missense Variants 50%
• Population Allele Frequencies 50%
• Variant Impact 50%
• Normal Population 50%
• Gain-of-function 50%
• GnomAD 50%
• Pathogenicity Test 50%
• Synonymous Variant 50%

Biochemistry, Genetics and Molecular Biology

• Gene Frequency 100%
• Single-Nucleotide Polymorphism 100%
• Deep Sequencing 33%
• Human Genome 33%
• Missense 33%
• Exome 33%

Neuroscience

• Allele Frequency 100%
• Single-Nucleotide Polymorphism 100%
• Deep Sequencing 33%
• Machine Learning Algorithm 33%