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Sections/parameters of the ACMG criteria that are evaluated/not... | Download Scientific Diagram
Cruxome: a powerful tool for annotating, interpreting and reporting genetic variants | BMC Genomics | Full Text
ACMG 2019 | Genomenon
The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice - ScienceDirect
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InterVar tool to predict variant pathogenicity - YouTube
Announcing the Release of Mastermind ACMG Interpretation Tool
The list of available bioinformatics tools for mtDNA analysis. | Download Table
ASHG 2021 Poster: Automated classification of copy number variants based on 2019 ACMG standards - bionanogenomics
SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation | Human Genomics | Full Text
GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss | PLOS Computational Biology
GitHub - WGLab/InterVar: A bioinformatics software tool for clinical interpretation of genetic variants by the 2015 ACMG-AMP guideline
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ACMG/AMP guidelines for the use of computational and prediction... | Download Scientific Diagram
Frontiers | Insights on variant analysis in silico tools for pathogenicity prediction
ClassifyCNV: a tool for clinical annotation of copy-number variants | Scientific Reports
We Are Headed to ACMG 2023! | The Golden Helix Blog
Genetics in Medicine
ACMG on X: "ACMG publishes new ACMG Therapeutics Bulletin: “Omaveloxolone approved for patients aged 16 years and older with Friedreich ataxia (FRDA)” in GIM Open, the College's gold open access journal: https://t.co/43F9LEoG1S #
GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss | PLOS Computational Biology