Table 1.
Software |
Version |
Summary |
---|---|---|
Abricate |
1.0.1 |
Detection of antimicrobial resistance genes, plasmids and virulence factors |
AMRfinder |
3.8.4 |
Detection of antimicrobial resistance genes from assembled contigs |
Any2fasta |
0.4.2 |
Converts any genomic data format to fasta format |
Assembly-stats |
1.0.1 |
Summarizes quality assembly metrics from contigs |
Biopython.convert |
1.0.3 |
Conversion and manipulation of different genomic data formats |
BMGE |
1.12 |
Block mapping and gathering with entropy for removal of ambiguously aligned reads from multiple sequence alignments |
BWA |
0.7.17 |
Burrow–Wheeler algorithm for fast alignment of short sequence reads |
Cairosvg |
2.4.2 |
Converts SVG to PDF and PNG formats |
Fastqc |
0.11.9 |
Quality control and visualization of HTS data |
Fasttree |
2.1.10 |
Ultra-fast inference of phylogeny using the maximum-likelihood method |
Freebayes |
1.3.2 |
Bayesian-based haplotype prediction of nucleotide variants |
ISMapper |
2.0.1 |
Detection of insertion sequences within genomes |
IQtree |
2.0.3 |
Inference of phylogeny using the maximum-likelihood method |
Kleborate |
1.0.0 |
Screening for AMR genes and MLSTs from genome assemblies |
Lxml |
4.5.2 |
Parsing of XML and HTML using Python |
Mafft |
7.471 |
Algorithm for performing multiple sequence alignments |
Multiqc |
1.9 |
Aggregates numerous HTML quality reports into a single file |
Megahit |
1.2.9 |
Ultra-fast genome assembly algorithm |
Mlst |
2.19.0 |
Characterization and detection of clones within a population of pathogenic isolates |
Nextflow |
20.07.1 |
Portable next-generation workflow language that enables reproducibility and development of pipelines |
Parallel |
20200722 |
Executes jobs in parallel |
Prinseq |
0.20.4 |
Trims, filters and reformats genomic sequence data |
Prodigal |
2.6.3 |
Prediction of protein-coding genes in prokaryotic genomes |
Prokka |
1.14.6 |
Fast and efficient annotation of prokaryotic assembled genomes |
Quast |
5.0.2 |
Quality assembly assessment tool |
Roary |
3.13.0 |
Large-scale pangenome analysis |
R-base |
4.0.2 |
Statistical data computing and graphical software |
Samclip |
0.4.0 |
Filters SAM file for soft and hard clipped alignments |
Samtools |
1.9 |
Tools for manipulation of next-generation sequence data |
Shovill |
1.0.9 |
Illumina short-read assembler for bacterial genomes |
Snippy |
4.3.6 |
Rapid haploid bacterial variant caller |
Snpeff |
4.5covid19 |
Functional effect and variant predictor suite |
SRA-tools |
2.10.8 |
Toolbox for acquisition and manipulation of sequences from the NCBI |
Trimmomatic |
0.39 |
Illumina short-read adapter trimming algorithm |
Unicycler |
0.4.8 |
A hybrid assembly pipeline for Illumina and long-read sequence data |
Vt |
2015.11.10 |
A tool for normalizing variants in genomic sequence data |