Polyphen2 drug

Aliases

PolyPhen-2, PolyPhen2 [HDIV], Polyphen2 HDIV

External links

DrugBank · PubChem

Related entities (1)

Mentioned in (24)

Papers in which this entity is mentioned.

• CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods. (2024)
• Multi-cancer analysis of clonality and the timing of systemic spread in paired primary tumors and metastases. (2020)
• dbNSFP v4: a comprehensive database of transcript-specific functional predictions and annotations for human nonsynonymous and splice-site SNVs. (2020)
• De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. (2020)
• The GenomeAsia 100K Project enables genetic discoveries across Asia. (2019)
• Comprehensive Characterization of Cancer Driver Genes and Mutations. (2018)
• GAVIN: Gene-Aware Variant INterpretation for medical sequencing. (2017)
• Evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines. (2017)
• CScape: a tool for predicting oncogenic single-point mutations in the cancer genome. (2017)
• De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
• New insights into the generation and role of de novo mutations in health and disease. (2016)
• De novo variants in sporadic cases of childhood onset schizophrenia. (2016)
• REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants. (2016)
• The human gene damage index as a gene-level approach to prioritizing exome variants. (2015)
• Genetic linkage analysis in the age of whole-genome sequencing. (2015)
• MBASED: allele-specific expression detection in cancer tissues and cell lines. (2014)
• Genome-wide association discoveries of alcohol dependence. (2014)
• Candidate gene association studies: a comprehensive guide to useful in silico tools. (2013)
• The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
• Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
• Annotation of functional variation in personal genomes using RegulomeDB. (2012)
• Evolution and functional impact of rare coding variation from deep sequencing of human exomes. (2012)
• Cancer-specific high-throughput annotation of somatic mutations: computational prediction of driver missense mutations. (2009)
• SNPs3D: candidate gene and SNP selection for association studies. (2006)

Merged raw entities (5)

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