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Pathogen Informatics, Wellcome Sanger Institute's Projects

panito icon panito

Calculate genome wide average nucleotide identity (gwANI) for a multiFASTA alignment

plasmidtron icon plasmidtron

Assembling the cause of phenotypes and genotypes from NGS data

pymummer icon pymummer

Python3 module for running MUMmer and reading the output

roary icon roary

Rapid large-scale prokaryote pan genome analysis

saffrontree icon saffrontree

SaffronTree: Reference free rapid phylogenetic tree construction from raw read data

seroba icon seroba

k-mer based Pipeline to identify the Serotype from Illumina NGS reads

singularity-bsub icon singularity-bsub

Provides wrapper scripts for executing LSF commands within a Singularity container

snp-sites icon snp-sites

Finds SNP sites from a multi-FASTA alignment file

snpeffwrapper icon snpeffwrapper

Takes a VCF and applies annotations from a GFF using SnpEff

software-tracker icon software-tracker

API and helper scripts for the pathogen software installation tracking database

tprnaseq icon tprnaseq

A bacterial RNAseq pipeline, designed for analysis of Treponema pallidum data

unix-training icon unix-training

A set of jupyter notebooks to provide unix training developed by Pathogen Informatics at Wellcome Sanger Institute.

vr-codebase icon vr-codebase

The overall codebase developed and used by the Vertebrate Resequencing group at the Sanger Institute

writedb_entry_set icon writedb_entry_set

Repo to hold the writedb_entry_set Python code extracted from the Pathogen Informatics general GitLab repo.

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