Software tools for manipulating and adding annotations to variant... | Download Scientific Diagram
Novel scripts for improved annotation and selection of variants from whole exome sequencing in cancer research - ScienceDirect
Variant calling and annotation
Genetic Clinics
ClassifyCNV: a tool for clinical annotation of copy-number variants | Scientific Reports
GitHub - vatlab/varianttools: software tool for the manipulation, annotation, selection, and analysis of variants in the context of next-gen sequencing analysis
Variant filtering and annotation workflow. The analysis pipeline... | Download Scientific Diagram
Annotation Tool Comparison. | Download Table
Transcript expression-aware annotation improves rare variant interpretation | Nature
Genes | Free Full-Text | iVar, an Interpretation-Oriented Tool to Manage the Update and Revision of Variant Annotation and Classification
A performance evaluation study: Variant annotation tools - the enigma of clinical next generation sequencing (NGS) based genetic testing - ScienceDirect
Summary of the main variant annotation tools for non-coding DNA regions | Download Table
ANNOVAR - Wikipedia
VCF Annotation Tools (VAtools) — VCF Annotation Tools (VAtools) 5.1.1 documentation
Protocol for unbiased, consolidated variant calling from whole exome sequencing data - ScienceDirect
Variant Detection Analysis Software – Partek Inc
SNP/Variant Calling Tutorial
ANNOVAR - Wikipedia
Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR | Nature Protocols
Frontiers | Insights on variant analysis in silico tools for pathogenicity prediction
Variant annotation
BasePlayer manual
Variant prioritization with Gemini | In-depth-NGS-Data-Analysis-Course
10. Variants-of-interest — Genomics Tutorial 2020.2.0 documentation
