Repository macaron
Name: macaron
Owner: waqas
Synopsis: A python framework to identify and re-annotate multi-base affected codons in whole genome/exome sequence data
Predicted deleteriousness of coding variants is a frequently used criterion to filter out variants detected in next-generation sequencing projects and to select candidates impacting on the risk of human diseases. Most available dedicated tools implement a base-to-base annotation approach that could be biased in presence of several variants in the same genetic codon. We here proposed the MACARON program that, from a standard VCF file, identifies, re-annotates and predicts the amino acid change resulting from multiple single nucleotide variants (SNVs) within the same genetic codon.
Type: unrestricted
Revision: 0:c9636a827049
This revision can be installed: False
Times cloned / installed: 209

Categories
Genome annotation - Tools for annotating genomic information
Sequence Analysis - Tools for performing Protein and DNA/RNA analysis
Tool Dependency Packages - Repositories that contain third-party tool dependency package installation definitions
Variant Analysis - Tools for single nucleotide polymorphism data such as WGA