Topic: snpeff Goto Github
Some thing interesting about snpeff
Some thing interesting about snpeff
snpeff,Highly Open Workflow for Annotation & Ranking toward genomic variant Discovery
User: bioinfo-chru-strasbourg
snpeff,Generate an interactive HTML-based report from M.tb SnpEff annotated VCF(s)
Organization: combat-tb
snpeff,A tool to import SnpEff annotated files to a Neo4j Graph database
Organization: combat-tb
snpeff,Genomic Analysis Pipeline: Automate data preprocessing, variant calling, and annotation with Snakemake. Ensure reproducibility and reliability in genomic studies.
User: orangepomeranian
snpeff,A collection of scripts for filtering annotated variant call format files
Organization: scholl-lab
snpeff,HgvsGo is a program designed for analyzing "c." and "p." HGVS (Human Genome Variation Society) notations for single nucleotide variations (SNVs) and small insertions/deletions (indels) after variant calling. It serves as an alternative to tools like snpEff and VEP.
User: soloedward
snpeff,Snakemake workflow designed to annotate VCF files withe SnpEff / SniSift
User: tdayris-perso
snpeff,Multi-bAse Codon-Associated variant Re-annotatiON (MACARON)
User: waqasuddinkhan
Home Page: http://www.genmed.fr/images/publications/data/MACARON_GenMed.zip
snpeff,The AlleleCatalog pipeline is built for generating Allele Catalog datasets using next-generation sequencing (NGS) based genetic data and metadata.
User: yenon118
Home Page: https://github.com/yenon118/AlleleCatalog
snpeff,The PhenoDist pipeline is built for generating phenotype distributions for alleles in variant positions and utilizing statistical methods to test for variant position significance.
User: yenon118
Home Page: https://github.com/yenon118/PhenoDist
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