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InterVar is a bioinformatics software tool for clinical interpretation of genetic variants by the ACMG/AMP 2015 guideline.
InterVar is a bioinformatics software tool for clinical interpretation of genetic variants by the ACMG/AMP 2015 guideline.
A bioinformatics software tool for clinical interpretation of genetic variants by the 2015 ACMG-AMP guideline - WGLab/InterVar.
Feb 2, 2017 · InterVar can take a pre-annotated or VCF file as input and generate automated interpretation on 18 criteria. Furthermore, we have developed a companion web server, wInterVar, to enable user-friendly variant interpretation with an automated interpretation step and a manual adjustment step.
InterVar is a bioinformatics software tool for clinical interpretation of genetic variants by the ACMG/AMP 2015 guideline.
InterVar is bioinformatics software tool for clinical interpretation of genetic variants by the ACMG-AMP 2015 guidelines, which are published by the American College of Medical Genetics and Genomics (ACMG) and the Association for Molecular Pathology (AMP).
InterVar is a bioinformatics software tool for clinical interpretation of genetic variants by the ACMG2015 guideline. The input to InterVar is an annotated file generated from ANNOVAR, while the output of InterVar is the classification of variants into 'benign', 'likely benign', 'VUS', 'likely pathogenic' and 'pathogenic', together with ...
Jan 26, 2017 · InterVar is a free online bioinformatic tool and variant database which is built for variant interpretation based on the American College of Medical Genetics and Genomics and the Association for...
InterVar is a software tool to aid the clinical interpretation of sequence variants according to the 2015 American College of Medical Genetics and Genomics (ACMG) and the Association for Molecular Pathology (AMP) guidelines. A web-based version, winterVar, is available at http://wintervar.wglab.org.
InterVar is a bioinformatics software tool for clinical interpretation of genetic variants by the ACMG/AMP 2015 guideline. The input to InterVar is an annotated file generated from ANNOVAR, while the output of InterVar is the classification of variants into 'Benign', 'Likely benign', 'Uncertain significance', 'Likely pathogenic' and 'Pathogenic ...
